Viewpoint: An argument for CRISPR crops ‘Very little about modern life is natural and it’s time we all got over it’ – Genetic Literacy Project

Life goes on as gene-edited foods begin to hit the market. Japanese consumers have recently started buying tomatoes that fight high blood pressure, and Americanshave been consuming soyengineered to produce high amounts of heart-healthy oils for a little over two years. Few people noticed these developments because, as scientists have said for a long time, the safety profile of a crop is not dictated by the breeding method that produced it. For all intents and purposes, it seems that food-safety regulators have done a reasonablejob of safeguarding public health against whatever hypothetical risks gene editing may pose.Credit: Karuchibe

But this has not stopped critics of genetic engineering from advocating for more federal oversight of CRISPR and othertechniquesused to make discrete changes to the genomes of plants, animals and other organisms we use for food or medicine. Over at The Conversation, a team of scientists recently made the case for tighter rules inCalling the latest gene technologies natural is a semantic distraction they must still be regulated.

Many scientists have defended gene editing, in part, by arguing that it simply mimics nature. A mutation that boosts the nutrient content of rice, for example, is the same whether it was induced by a plant breeder or some natural phenomenon. Indeed, the DNA of plants and animals we eatcontains untold numbersof harmless, naturally occurringmutations. But The Conversation authors will havenone of this:

Unfortunately, the risks from technology dont disappear by calling it natural Proponents of deregulation of gene technology use the naturalness argument to make their case. But we argue this is not a good basis for deciding whether a technology should be regulated.

They have written a very longpeer-reviewed articleoutlining a regulatory framework based on scale of use.The ideais that the more widely a technology is implemented, the greater risk it may pose to human health and the environment, which necessitates regulatory control points to ensure its safe use. Its an interesting proposal, but its plagued by several serious flaws.

The most significant issue with a scale-based regulatory approachis that its a reaction to risks that have never materialized. This isnt to say that a potentially harmful genetically engineered organism will never be commercialized. But if were going to upend our biotechnology regulatory framework, we need to do so based on real-world evidence. Some experts have actually argued, based on decades of safety data, that the US over-regulates biotech products. As biologist and ACSHadvisorDr. Henry Miller and legal scholar John Cohrssen wroterecently in Nature:

After 35 years of real-world experience with genetically engineered plants and microorganisms, and countless risk-assessment experiments, it is past time to reevaluate the rationale for, and the costs and benefits of, the case-by-case reviews of genetically engineered products now required by the US Environmental Protection Agency (EPA), US Department of Agriculture (USDA) and US Food and Drug Administration (FDA).

Real-world data aside for the moment, there are some theoretical problems with the scalabilitymodel as well. Theargument assumes thatrisks associated with gene editing proliferate as use of the technology expands, because each gene edit carries a certain level of risk. This is a false assumption, as plant geneticist Kevin Folta pointed out on a recentepisode of the podcastwe co-host (21 minute mark).

Scientists have a variety of tools with which to monitor and limit the effects of specific gene edits. For example,proteins known asanti-CRISPRs can be utilized to halt the gene-editing machinery so it makes only the changes we want it to. University of Toronto biochemist Karen Maxwell has explained how this couldwork in practice:

In genome editing applications, anti-CRISPRs may provide a valuable off switch for Cas9 activity for therapeutic uses and gene drives. One concern of CRISPR-Cas gene editing technology is the limited ability to control its activity after it has been delivered to the cell . which can lead to off-target mutations. Anti-CRISPRs can potentially be exploited to target Cas9 activity to particular tissues or organs, to particular points of the cell cycle, or to limit the amount of time it is active

Suffice it to say that these and other safeguards significantly alter the risk equation and weaken concerns about a gene-edits-gone-wild scenario. Parenthetically, scientists design these sorts of preventative measures as they developmoregenetic engineering applications for widespread use. This is why the wide variety of cars in production todayhave safety featuresthat would have been unheard of in years past.

To bolster their argument, The Conversation authors made the following analogy:

Imagine if other technologies with the capacity to harm were governed by resemblance to nature. Should we deregulate nuclear bombs because the natural decay chain of uranium-238 also produces heat, gamma radiation and alpha and beta particles? We inherently recognize the fallacy of this logic. The technology risk equation is more complicated than a supercilious its just like nature argument

If someone has to resort to this kind of rhetoric, the chances are excellent that their argument is weak. Fat Man and Little Boy,the bombs droppedon Japan in 1945, didnt destroy two cities because a nuclear physicist in New Mexico made a technical mistake. These weapons are designed to wreak havoc. Tomatoes bred to produce more of an amino acid, in contrast, are not.

The point of arguing that gene-editing techniques mimic natural processes isnt to assert that natural stuff is good; therefore, gene editing is also good. Instead, the point is to illustrate that inducing mutations in the genomes of plants and animals is not novel or uniquely risky. Even the overpriced products marketed as all-naturalhave been improvedby mutations resulting from many years of plant breeding.

Nonetheless, some scientistshave arguedthat reframing the gene-editing conversation in terms of risk vs benefit would be a smarter approach than making comparisons to nature. I agree with them, so lets start now. The benefits of employing gene editing to improve our food supply and treat disease far outweigh the potential risks, which we can mitigate. Very little about modern life is naturaland its time we all got over it.

Cameron J. English is the director of bio-sciences at theAmerican Council on Science and Health. Visithis websiteand follow ACSH on Twitter@ACSHorg

A version of this article was originally posted at theAmerican Council on Science and Healthand is reposted here with permission. The American Council on Science and Health can be found on Twitter@ACSHorg

Go here to see the original:

Viewpoint: An argument for CRISPR crops 'Very little about modern life is natural and it's time we all got over it' - Genetic Literacy Project

New gene-writing technology to obtain more effective and safe therapies developed – EurekAlert

image:From left to right: Marc Gell, Dimitrije Ivani, Avencia Snchez-Mejas and Maria Pallars. view more

Credit: UPF

An international, multidisciplinary team of researchers from theTranslational Synthetic Biology Laboratoryat Pompeu Fabra University (Barcelona, Spain), led by Dr.Marc Gell, has published an article in the scientific journalNature Communicationsshowing the potential of Find Cut-and-Transfer (FiCAT) technology as a state-of-the-art tool forgene writingto develop advanced therapies that are safer and more effective in their future clinical application in patients withgenetic and oncological diseasesthat have few treatment options.

The UPF Translational Synthetic Biology Laboratory has been working on gene editing and synthetic biology applied to gene therapies since 2017. FiCAT technology is an important scientific breakthrough to overcome the current limitations of the technology used today for genome editing and gene therapy.

Human genome engineering has significantly progressed in the last decade with the development of new editing tools, but there was still a technology gap that would allow therapeutic genes to be transferred efficiently with few size limitations, comments Dr. Marc Gell, supervisor of the study.

In this work, the researchers develop an efficient and precise programmable gene writing technology based on the combination of modified proteins CRISPR-cas and piggy Bac transposase (PB), succeeding in inserting small and large fragments. Dr.Maria Pallars, co-first author of the study explains that: CRISPR stands out for its precision when editing small fragments. However, transposases allow us to insert large fragments but in an uncontrolled manner. We have combined the best of each technology.

In this way, FiCAT technology allows us to precisely insert large fragments of DNA into the genome. This means we can develop therapeutic solutions to diseases that currently have no treatment, such as Duchenne muscular dystrophy, or some cases of hereditary blindness, in which the affected gene is large in size, asserts Dr.Avencia Snchez-Mejas, a senior researcher with the group and co-supervisor of the work.

They tested the technology in human and mouse cell lines achieving efficiencies of 522% with minimal off-target insertions and have demonstrated on-target gene transfer in vivo in mouse liver and germline cells in mouse models. Lastly, they performed a directed evolution of FiCAT and further improved efficiency by 25-30%. We have been progressively modifying enzymes so that they acquire the function we were looking for, selecting the ones that displayed a better function, detailsDimitrije Ivani, co-first author of the article. Our work is a clear example that enzyme engineering in the context of genome editing has great potential, he concludes.

UPF has transferred FiCAT technology via the spinoffIntegra Therapeutics, founded in 2020 by the researchers Marc Gell and Avencia Snchez-Mejas, seeking to get this scientific knowledge and technological capacity to reach the biopharmaceutical industry to develop safe and efficient advanced technologies that reach patients. Recently, Integra Tx has obtained 4.5 million euros in funding from Advent France Biotechnology (France), Invivo Capital (Spain) and Takeda Ventures (USA).

The work published in Nature Communications was carried out with funding from the Societal challenges AEI, AGAUR- PRODUCTE, UPGRADE-Horizon 2020 of the European Commission; la Caixa CaixaImpulse Validate and CaixaImpulse Consolidate programmes; the Ramn Areces Foundation; and the Ramn y Cajal programme of the Spanish Ministry of Economy, Industry and Competitiveness.

Reference article:

Pallars-Masmitj, M; Ivani, D; Mir-Pedrol, J; Jaraba-Wallace, J; Tagliani, T; Oliva, B; Snchez-Mejas, A; Gell, M. Find and cut-and-transfer (FiCAT) mammalian genome engineering. Nature Communications (2021). DOI: 10.1038/s41467-021-27183-x.

Nature Communications

Experimental study

Cells

Find and cut-and-transfer (FiCAT) mammalian genome engineering

3-Dec-2021

A.S.-M., D.I., M.G. and M.P.-M. have filed patent applications on FiCAT technology. Patent applicant: Pompeu Fabra University; application number: PCT/IB2020/055507; status of application: pending; specific aspect of manuscript covered in patent application: this patent application covered the general aspects of DNA binding proteins fused to integrases and transposases. Specifically, Fig. 1b, Supplementary Fig. 2a and preliminary data on activity characterization of some of the hyPB mutants included in Fig. 1c, d were disclosed in this patent application. A.S.-M. and M.G. are shareholders of Integra Therapeutics, company that licensed FiCAT technology. The remaining authors declare no competing interests.

Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.

Read this article:

New gene-writing technology to obtain more effective and safe therapies developed - EurekAlert

Researchers Dig Up Genes and Cells Related to Skull Formation in Mice – Genetic Engineering & Biotechnology News

In a new mouse study, scientists at the Icahn School of Medicine at Mount Sinai demonstrate how the activity of one gene, turned on in a newly discovered group of bone-bordering cells, may play an important role in shaping the skull.

The findings are published in the journalNature Communications in a paper titled, Single-cell analysis identifies a key role for Hhip in murine coronal suture development, and led by Greg Holmes, PhD, assistant professor of genetics and genomic sciences at Icahn Mount Sinai.

Craniofacial development depends on formation and maintenance of sutures between bones of the skull, the researchers wrote. In sutures, growth occurs at osteogenic fronts along the edge of each bone, and suture mesenchyme separates adjacent bones. Here, we perform single-cell RNA-seq analysis of the embryonic, wild type murine coronal suture to define its population structure.

Researchers focused on the cells of the coronal suture, a fibrous joint that connects the front and middle bone plates.

The Holmes lab worked with researchers in the labs of Bin Zhang, PhD, Harm van Bakel, PhD, and Ethylin Wang Jabs, MD, of Icahn Mount Sinai. Together they studied how the genetic activity in the cells of the coronal suture changes during early development.

Their findings suggested that a gene encoding a molecule called hedgehog interacting protein (HHIP) plays a unique role in coronal suture development. The researchers observed the gene was more active in a novel group of mesenchyme cells than it was in osteoblasts.

Using single-cell with bulk RNA-seq analysis we have better defined the distinctive composition of the coronal suture at the transcriptional and cell population levels, the researchers wrote.

Looking toward the future, the researchers hope that advanced single-cell genetic studies like this one will pave the way for a more thorough understanding of how a skull is shaped under healthy and disease conditions.

Our transcriptomic approach greatly expands opportunities for hypothesis-driven research in coronal and other suture development, concluded the researchers.

See more here:

Researchers Dig Up Genes and Cells Related to Skull Formation in Mice - Genetic Engineering & Biotechnology News

Nature Communications paper published by two collaborating teams at Clarkson University (NY, USA) and Queensland University of Technology (Australia)…

Figure 1. Leading researchers in the collaborative project. The full list of the co-authors in the Nature Communication paper: Zhong Guo, Oleh Smutok, Wayne A. Johnston, Patricia Walden, Jacobus P. J. Ungerer, Thomas S. Peat, Janet Newman, Jake Parker, Tom Nebl, Caryn Hepburn, Artem Melman, Richard J. Suderman, Evgeny Katz, Kirill Alexandrov.

The best and most efficient way to perform multi-disciplinary research is by doing it in collaboration. One of such research programs, including synthetic biology, materials science, bioelectrochemistry, bioelectronics, and biosensors, has been performed in a close collaboration between scientists at the Department of Chemistry and Biomolecule Science, Clarkson University, Dr. Oleh Smutok, Dr. Artem Melman (deceased on November 25, 2021), and Dr. Evgeny Katz, with a team of Australian scientists led by Dr. Kirill Alexandrov, Queensland University of Technology (Figure 1). This collaboration being active for several years has been supported with grants from Human Frontiers Science Program (HFSP) and US Department of Defense with the total funding over 1 million dollars. The results from the collaborative efforts have been published in numerous scientific papers and covered by several patents. The most recent and impressive publication was a paper in Nature Communications one of the top scientific journals (Impact Factor 14.92). The paper entitled Design of a methotrexate-controlled chemical dimerization system and its use in bio-electronic devices (Nature Commun. 2021, 12 article No. 7137) reports on a novel artificial enzyme produced by genetic engineering that can be activated with a drug (methotrexate) molecules. The artificial enzyme was immobilized at an electrode surface and used for the drug biosensing with extremely high sensitivity and specificity (Figure 2).

In addition to the fundamental novelty of using the artificial signal-activated enzyme, the study is highly relevant for practical biomedical application. Methotrexate is a toxic drug used in anti-cancer chemotherapy and its overdose has serious, life-threatening side effects. Thus, the methotrexate analysis in biological fluids is important for keeping the drug at the optimal concentration. The study opens the future options for biomedical applications of the developed biosensor and possibilities for other biosensing systems based on the same concept. It should be noted that the success of this project was based on the collaboration of scientists with expertise in different areas, synthetic biology, synthetic organic chemistry, and bioelectrochemistry. This is an exemplary collaboration that serves as a model of performing multi-disciplinary research. While the artificial enzyme preparation was carried out by the Australian team led by Dr. Alexandrov, the bioelectrochemical study of the developed biosensor was performed by Dr. Smutok at Clarkson University. Both US and Australian teams are continuing their successful work combining synthetic biology and bioelectronics and are expecting many more interesting and practically important results. The scientific efforts are combined with the education of graduate and undergraduate students participating in the project.

Originally posted here:

Nature Communications paper published by two collaborating teams at Clarkson University (NY, USA) and Queensland University of Technology (Australia)...

Poseida Therapeutics Provides Update on BCMA-Targeted CAR-T Clinical Trials at the 2021 American Society of Hematology (ASH) Annual Meeting – Yahoo…

P-BCMA-101 demonstrated strong anti-tumor activity and was well tolerated in nearly 100 patients with R/R multiple myeloma at the time of data cutoff

P-BCMA-101 in combination with rituximab achieved an improved overall response rate of 78% and 100% overall survival

Learnings from P-BCMA-101 informed development of the Company's first fully allogeneic CAR-T product candidate, P-BCMA-ALLO1

SAN DIEGO, Dec. 13, 2021 /PRNewswire/ -- Poseida Therapeutics, Inc. (Nasdaq: PSTX), a clinical-stage biopharmaceutical company utilizing proprietary genetic engineering platform technologies to create cell and gene therapeutics with the capacity to cure, today reported interim results from its Phase 1/2 PRIME clinical trial of P-BCMA-101 for the treatment of relapsed/refractory multiple myeloma (R/R MM) at the 2021 American Society of Hematology (ASH) Annual Meeting.

Poseida Therapeutics (PRNewsfoto/Poseida Therapeutics, Inc.)

The results show that P-BCMA-101, a non-viral transposon-based autologous CAR-T, was well tolerated and demonstrated strong anti-tumor activity in advanced, late line R/R MM patients. The learnings from P-BCMA-101 informed the development of the Company's first allogeneic program, P-BCMA-ALLO1 which is also being evaluated in R/R MM patients. The Company previously announced that it is winding down the P-BCMA-101 autologous program in favor of the allogeneic program, P-BCMA-ALLO1.

"We are encouraged by the outcomes seen from our clinical trial of P-BCMA-101, results that continue to validate our approach and that have informed P-BCMA-ALLO1, our first fully allogeneic CAR-T program for patients with multiple myeloma, as well as our other programs. Our focus is on creating differentiated product candidates with a high percentage of T stem cell memory (Tscm) cells," said Eric Ostertag, M.D., Ph.D., chief executive officer of Poseida Therapeutics. "Looking ahead, we continue to advance P-BCMA-ALLO1 and P-MUC1C-ALLO1 and look forward to presenting data in 2022 for both of these allogeneic programs."

Story continues

The PRIME trial is a Phase 1/2, open label 3+3 single dose escalation of P-BCMA-101 CAR-T cells. The primary objective of the study is to determine the safety and maximum tolerated dose of P-BCMA-101 based on dose limiting toxicities (DLT), and the key secondary objective is to assess the anti-myeloma effect of the product. The median patient age was 62, with a median time since diagnosis of approximately 5.8 years. Patients were heavily pre-treated, with a median of 7 prior lines of therapy (2-18). As of the data cut-off date of October 15, 2021, a total of 98 patients have been dosed with P-BCMA-101.

The best observed treatment regimen was a combination with rituximab (n=14), with an overall response rate (ORR) of 78%, a VGPR/sCR rate of 43% and 100% overall survival at the time of the data cutoff. Progression free survival was also improved with rituximab, with median overall survival rates not yet reached in several cohorts including the rituximab combination cohorts. Response rates for other cohorts are consistent with results previously reported.

Across the study, no dose-limiting toxicities were observed. 28% of patients developed cytokine release syndrome (CRS) and 7% of patients developed neurotoxicity. None of the patients developed Grade 3 or higher CRS, and 2% of patients developed Grade 3 neurotoxicity. There were no treatment-related deaths among the patient population and no patients needed ICU admission as a result of CAR-T related toxicities. 28 patients were treated on a fully outpatient basis.

"P-BCMA-101 demonstrated strong anti-tumor activity in advanced multiple myeloma patients, and cohorts to date have shown minimal CRS and neurotoxicity, which allows for safe administration in an outpatient environment and combinations with other therapies," said Caitlin Costello, M.D., Associate Clinical Professor of Medicine and member of the Division of Blood and Marrow Transplantation at the University of California, San Diego. "These data indicate that the piggyBac transposon-based platform is an attractive option for allogeneic CAR-T cells, which has led to a first-in-human Phase 1 study."

The Company's first fully allogeneic CAR-T cell product, P-BCMA-ALLO1 utilizes Poseida's proprietary piggyBac DNA delivery system and Cas-CLOVER site-specific gene editing system to create an allogeneic product that prevents both graft-vs-host and host-vs-graft diseases and also incorporates a next-generation BCMA binder. P-BCMA-ALLO1 manufacturing involves a proprietary "booster" molecule that allows for numerous doses to be produced from a single manufacturing run, while maintaining desirable Tscm cells, which can reach percentages in the 60-80% range.

The Investigational New Drug (IND) application for P-BCMA-ALLO1 was given a safe to proceed designation by the FDA in August 2021. The Phase 1 study is an open label, dose escalation study following a 3+3 design of dose escalation in subjects with R/R MM. The study will assess the safety and maximum tolerated dose of P-BCMA-ALLO1 based on dose limiting toxicities. Key secondary objectives of the study include the anti-myeloma effect and safety of P-BCMA-ALLO1.

About Poseida Therapeutics, Inc.Poseida Therapeutics is a clinical-stage biopharmaceutical company dedicated to utilizing our proprietary genetic engineering platform technologies to create next generation cell and gene therapeutics with the capacity to cure. We have discovered and are developing a broad portfolio of product candidates in a variety of indications based on our core proprietary platforms, including our non-viral piggyBac DNA Delivery System, Cas-CLOVER Site-specific Gene Editing System and nanoparticle- and AAV-based gene delivery technologies. Our core platform technologies have utility, either alone or in combination, across many cell and gene therapeutic modalities and enable us to engineer our portfolio of product candidates that are designed to overcome the primary limitations of current generation cell and gene therapeutics. To learn more, visit http://www.poseida.com and connect with us on Twitter and LinkedIn.

Forward-Looking StatementStatements contained in this press release regarding matters that are not historical facts are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include statements regarding, among other things, the potential benefits of Poseida's technology platforms and product candidates, Poseida's plans and strategy with respect to developing its technologies and product candidates, and anticipated timelines and milestones with respect to Poseida's development programs and manufacturing activities. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. These forward-looking statements are based upon Poseida's current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, risks and uncertainties associated with development and regulatory approval of novel product candidates in the biopharmaceutical industry and the other risks described in Poseida's filings with the Securities and Exchange Commission. All forward-looking statement contained in this press release speak only as of the date on which they were made. Poseida undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law.

Cision

View original content to download multimedia:https://www.prnewswire.com/news-releases/poseida-therapeutics-provides-update-on-bcma-targeted-car-t-clinical-trials-at-the-2021-american-society-of-hematology-ash-annual-meeting-301442793.html

SOURCE Poseida Therapeutics, Inc.

Original post:

Poseida Therapeutics Provides Update on BCMA-Targeted CAR-T Clinical Trials at the 2021 American Society of Hematology (ASH) Annual Meeting - Yahoo...

Genome Editing Market to hit US$ 10691.0 Million, Globally, by 2025 at 17.0% CAGR: The Insight Partners – Digital Journal

The global genome editing market is expected to reach US$ 10,691.0 million by 2025 from US$ 3,210.1 million in 2017; it is estimated to grow at a CAGR of 17.0% from 2018 to 2027.

According The Insight Partners study on Genome Editing Market Forecast to 2027 COVID-19 Impact and Global Analysis by Technology, Application, End User, The report highlights trends existing in the market, and drivers and hindrances pertaining to the market growth. Factors such as Increase in funding for the genome editing, rising prevalence of the genetic disorders, rise in the advancements for genome editing technology and rise in the production of genetically modified crops are the driving factors for the growth of the market.

Genome editing is a technique that is utilized for the changes that are to be done in the DNA of a cell or an organism. The technique involves cutting DNA sequences for the addition or removing the DNA in the genome. The changes in the genome are done for the required characteristics of the cell. Genome editing is done for the research purpose, the treatment of the diseases, and the biotechnological purpose.

Get Sample PDF Copy of Genome Editing Market at: https://www.theinsightpartners.com/sample/TIPHE100000853/

Market Insights

Increase in Funding for the Genome Editing

The market for genome editing is expected to grow in the coming near future due to the growth factor that is driving the market is the increase in the funding. The different government in the different regions are increasing their funds and grants to develop genome editing research. Owing to genome editings advantages, the various government is supporting their public and private research and academic institutes for increasing the research activities for the genome editing and genetic engineering.

Across the world, funding is being provided by every nation. However, the more funds, for instance, in January 2018 US government announced donating US$ 190 million for research for the next six years. Also, the government is hoping to develop therapies to treat cancer and other diseases using gene editing. In addition, the National Institutes of Health (NIH) has kept approximately US$ 45.5 million aside for the next four fiscal years for the Somatic Cell Genome Editing program. Moreover, in the Asia Pacific region, the countries are also investing more in the development of genome editing technology for two-three years back. For instance, in April 2016, Japan invested approximately US$76million for the five years for the creation of Japanese owned genome editing technologies.

Furthermore, the investments are made for private companies operating for genome editing. For instance, in August 2015, Editas Medicine is a company at the forefront of developing the gene-editing technology CRISPR has received US$ 120 million to create a new treatment for the conditions which include cancer, retinal diseases, and sickle cell anemia. Therefore, the rise in the funding for genome editing is likely to drive the market for genome editing in the forecast period. The rise in the funding will enhance the research and development of the gene-editing technologies and products for the researchers for efficient and effective genome editing. The funding will also enable the biopharmaceutical and pharmaceutical companies to develop technologies for the therapies using gene editing to treat and diagnose chronic diseases.

It also includes the impact of the COVID-19 pandemic on the market across all the regions. The Genome Editing Market , by region, is segmented into North America, Europe, Asia Pacific (APAC), Middle East and Africa (MEA), and South and Central America (SAM).

COVID-19 first began in Wuhan (China) during December 2019 and since then it has spread at a fast pace across the globe. The US, India, Brazil, Russia, France, the UK, Turkey, Italy, and Spain are some of the worst affected countries in terms confirmed cases and reported deaths. The COVID-19 has been affecting economies and industries in various countries due to lockdowns, travel bans, and business shutdowns.

Download the Latest COVID-19 Analysis on Genome Editing Market Growth Research Report at: https://www.theinsightpartners.com/covid-analysis-sample/TIPHE100000853

Based on technology, the genome editing market is segmented into transcription activator-like effector nucleases (TALENS), clustered regularly interspaced short palindromic repeats (CRISPR), zinc finger nucleases (ZFNs), antisense RNA and others. In 2017, the CRISPR segment held the largest share of the market, by technology owing to the applications and its benefits offered. The TALENs segment is expected to grow at the fastest rate during the coming years.

Based on application, the genome editing market is segmented into genetic engineering, cell line engineering and others. In 2017, cell line segment held the largest share of the market, by application. Moreover, the genetic engineering segment is expected to grow at the fastest rate during the coming years owing to its sub segments such as animal genetic engineering and plant genetic engineering that are being carried out extensively.

Based on end user, the genome editing market is segmented into biotechnology & pharmaceutical companies, contract research organizations, academic & government research organization and other end users. The market is dominated by the biotechnology & pharmaceutical companies and is expected to surge significantly during the forecast period from 2017 to 2025. The biotechnology & pharmaceutical companies segment is expected gain its market share during the forecast period. Also, biotech & pharmaceutical companies is expected to show a prime CAGR owing to the increasing government funding and partnerships between the various organizations in all the regions.

Genome Editing Market : Competitive Landscape and Key Developments

Transposagen Biopharmaceuticals, Inc.,Integrated DNA Technologies, Inc.,Thermo Fisher Scientific Inc.,GenScript,Lonza,Horizon Discovery Group plc,Sangamo Therapeutics, Inc.,New England Biolabs,Editas Medicine,Merck KGaA.

Order a Copy of Genome Editing Market Shares, Strategies and Forecasts 2021-2025 Research Report at https://www.theinsightpartners.com/buy/TIPHE100000853/

About Us:

The Insight Partners is a one stop industry research provider of actionable intelligence. We help our clients in getting solutions to their research requirements through our syndicated and consulting research services. We specialize in industries such as Semiconductor and Electronics, Aerospace and Defense, Automotive and Transportation, Biotechnology, Healthcare IT, Manufacturing and Construction, Medical Device, Technology, Media and Telecommunications, Chemicals and Materials.

Contact Us:

If you have any queries about this report or if you would like further information, please contact us:

Contact Person:Sameer Joshi

E-mail: sales@theinsightpartners.com

Phone:+1-646-491-9876

Press Release: https://www.theinsightpartners.com/pr/genome-editing-market/

Original post:

Genome Editing Market to hit US$ 10691.0 Million, Globally, by 2025 at 17.0% CAGR: The Insight Partners - Digital Journal

In 2022, Molecular Farming Startups Will Move Toward Commercialization of Animal-Free Proteins – The Spoon

Like many of the technologies that are driving innovation in the alternative protein space, plant molecular farming has traditionally been used in the pharmaceutical industry. The practice which involves genetically editing a crop so that its cells produce a desired protein is being discussed as a way to rapidly produce proteins for COVID-19 vaccines.

In the food industry, molecular farming is one route to producing the animal proteins that give egg, dairy, and meat products their visual, taste, and functional properties. Molecular farming allows you to use the exact same protein that would normally be produced by a chicken or cow, without the need for any actual animals.

Moolec Science, a spinoff of Argentina-based agtech company Bioceres Crop Solutions, is probably the most prominent name in molecular farming for the food industry. Moolec already sells chymosin, a cheesemaking enzyme, which the company grows in safflower plants. Theyve also successfully grown meat proteins in soybean and pea plants.

The Moolec team believes that molecular farming can help to bring down the end costs of alternative meat products. (Theres nothing better than low-tech farming to produce at an enhanced scale and low cost, company CEO and co-founder Gastn Paladini told The Spoon back in October.) And they may be right.

Molecular farming can help producers to avoid some of the costly and tricky problems of growing proteins in traditional bioreactors. When you use a plant as your bioreactor, as food scientist and thought leader Tony Hunter pointed out in an article this year, you dont need to worry about maintaining sterile conditions: Plants have built-in immune systems.

Moolec plans to launch its first animal-free meat protein in late 2022 or early 2023. The company is currently working toward regulatory approval for its products and its progress will be an interesting test of regulatory tolerance of Moolecs brand of genetic engineering.

One potential concern for regulators as they scrutinize molecular farming processes will be the possibility of gene flow from modified crops to related plants. Tiamat Sciences, a Belgium-based molecular farming startup, is limiting that possibility by growing its crops in a contained vertical farming system.

Tiamat has plans to expand alongside the cell-based meat industry. By targeting nascent markets on the verge of scale-up, weve already demonstrated significant traction for our solutions and an early revenue potential that is outstanding for a biotech startup, said Tiamats founder and CEO France-Emmanuelle Adil in a recent press release. The company currently produces GRAS-certified, animal-free growth factors for cultivated meat, and also manufactures proteins for the pharmaceutical industry.

Last month, Tiamat announced that it had raised a $3 million seed funding round led by Silicon Valley venture capital firm True Ventures. The company is using those funds to construct a pilot facility in Durham, N.C. so we may see them boost their capacity in the year to come.

Molecular farming startups still have some issues to work out. As Tony Hunter noted in his piece on molecular farming, plant tissue has larger and fewer protein-producing cells compared to the same volume of mammal tissue, making plants less productive as protein factories. And there are costs associated with extracting protein molecules from plants at the cellular level.

Still, the same upsides of molecular farming that make it attractive to the pharmaceutical industry will likely continue to spark interest from alternative protein producers especially as those producers seek ways to bring down the retail prices of their products.

Related

Read this article:

In 2022, Molecular Farming Startups Will Move Toward Commercialization of Animal-Free Proteins - The Spoon

The tomatoes at the forefront of a food revolution – BBC News

One 2021 study looked at the genome of Solanum sitiens a wild tomato species which grows in the extremely harsh environment of the Atacama Desert in Chile, and can be found at altitudes as high as 3,300m (10,826ft). The study identified several genes related to drought-resistance in Solanum sitiens, including one aptly named YUCCA7 (yucca are draught-resistant shrubs and trees popular as houseplants).

They are far from the only genes that could be used to give the humble tomato a boost. In 2020 Chinese and American scientists performed a genome-wide association study of 369tomato cultivars, breeding lines and landraces, and pinpointed a gene called SlHAK20 as crucial for salt tolerance.

Once the climate-smart genes such as these are identified, they can be targeted using Crispr to delete certain unwanted genes, to tune others or insert new ones. This has recently been done with salt tolerance, resistance to various tomato pathogens, and even to create dwarf plants which could withstand strong winds (another side effect of climate change). However, scientists such as Cermak go even further and start at the roots they are using Crispr to domesticate wild plant species from scratch, "de novo" in science speak. Not only can they achieve in a single generation what previously took thousands of years, but also with a much greater precision.

De novo domestication of Solanum pimpinellifolium was how Cermak and his colleagues at the University of Minnesota arrived at their 2018 plant. They targeted five genes in the wild species to obtain a tomato that would be still resistant to various stresses, yet more adapted to modern commercial farming more compact for easier mechanical harvesting, for example. The new plant also had larger fruits than the wild original.

"The size and weight was about double," Cermak says. Yet this still wasn't the ideal tomato he strives to obtain for that more work needs to be done. "By adding additional genes, we could make the fruit even bigger and more abundant, increase the amount of sugar to improve taste, and the concentration of antioxidants, vitamin C and other nutrients," he says. And, of course, resistance to various forms of stress, from heat and pests to draught and salinity.

See the original post here:

The tomatoes at the forefront of a food revolution - BBC News

Novavax Files for Emergency Use of COVID-19 Vaccine in the United Arab Emirates – KPVI News 6

GAITHERSBURG, Md., Dec. 13, 2021 /PRNewswire/ -- Novavax, Inc. (Nasdaq: NVAX), a biotechnology company dedicated to developing and commercializing next-generation vaccines for serious infectious diseases, today announced that it has submitted a regulatory filing to the Ministry of Health and Prevention (MoHaP) for emergency use of its COVID-19 vaccine in the United Arab Emirates (UAE).

"The rapid emergence and continuedspread of variants is a stark reminder that no one is safe until everyone is safe in the fight against COVID-19," said Stanley C. Erck, President and Chief Executive Officer, Novavax. "We remain committed to delivering our vaccine, which is based on a proven, well understood platform, to countries around the world as we anticipate that ongoing vaccination will be necessary over the long term to end the pandemic."

Novavax made the submission for the regulatory evaluation by MoHaP of NVX-CoV2373, the company's recombinant nanoparticle protein-based COVID-19 vaccine with Matrix-M adjuvant. The filing includes clinical data from two pivotal Phase 3 clinical trials: PREVENT-19, which included 30,000 participants in the U.S. and Mexico and demonstrated 100% protection against moderate and severe disease, 93.2% efficacy against the predominantly circulatingvariants of concern and variants of interest, and 90.4% efficacy overall; and a trial of 15,000 participants in the U.K. that demonstrated efficacy of 96.4% against the original virus strain, 86.3% against the Alpha (B.1.1.7) variant and 89.7% efficacy overall. In both trials, NVX-CoV2373 demonstrated a reassuring safety and tolerability profile.

Novavax and Serum Institute of India Pvt. Ltd. (SII) recently received Emergency Use Authorization (EUA) for the vaccine inIndonesiaand thePhilippines, and the companies have filed for EUA inIndiaand for Emergency Use Listing (EUL) with theWorld Health Organization(WHO). Novavax also announced regulatory filings for its vaccine in theUnited Kingdom,Australia,New Zealand,Canada, theEuropean Union, Singapore and with theWHO.Additionally, Novavax and SK bioscience announced a Biologics License Application (BLA)submission to MFDSinSouth Korea. Novavax expects to submit the complete package to the U.S. FDA by the end of the year.

The chemistry, manufacturing and controls (CMC) data package submitted to MoHaP and other global regulatory agencies leverages Novavax' manufacturing partnership with SII, the world's largest vaccine manufacturer by volume. It will later be supplemented with data from additional manufacturing sites in Novavax' global supply chain.

About the NVX-CoV2373 Phase 3 trials

NVX-CoV2373 is being evaluated in two pivotal Phase 3 trials: a trial in the U.K. that demonstrated efficacy of 96.4% against the original virus strain, 86.3% against the Alpha (B.1.1.7) variant and 89.7% efficacy overall; and the PREVENT-19 trial in the U.S. and Mexico that demonstrated 100% protection against moderate and severe disease, 93.2% efficacy against the predominantly circulatingvariants of concern and variants of interest, and 90.4% efficacy overall. It was generally well-tolerated and elicited a robust antibody response.

About NVX-CoV2373

NVX-CoV2373 is a protein-based vaccine candidate engineered from the genetic sequence of the first strain of SARS-CoV-2, the virus that causes COVID-19 disease. NVX-CoV2373 was created using Novavax' recombinant nanoparticle technology to generate antigen derived from the coronavirus spike (S) protein and is formulated with Novavax' patented saponin-based Matrix-M adjuvant to enhance the immune response and stimulate high levels of neutralizing antibodies. NVX-CoV2373 contains purified protein antigen and can neither replicate, nor can it cause COVID-19.

Novavax' COVID-19 vaccine is packaged as a ready-to-use liquid formulation in a vial containing ten doses. The vaccination regimen calls for two 0.5 ml doses (5 mcg antigen and 50 mcg Matrix-M adjuvant) given intramuscularly 21 days apart. The vaccine is stored at 2- 8 Celsius, enabling the use of existing vaccine supply and cold chain channels.

About Matrix-M Adjuvant

Novavax' patented saponin-based Matrix-M adjuvant has demonstrated a potent and well-tolerated effect by stimulating the entry of antigen-presenting cells into the injection site and enhancing antigen presentation in local lymph nodes, boosting immune response.

About Novavax

Novavax, Inc. (Nasdaq: NVAX) is a biotechnology company that promotes improved health globally through the discovery, development and commercialization of innovative vaccines to prevent serious infectious diseases. The company's proprietary recombinant technology platform harnesses the power and speed of genetic engineering to efficiently produce highly immunogenic nanoparticles designed to address urgent global health needs. NVX-CoV2373, the company's COVID-19 vaccine, received Emergency Use Authorization in Indonesia and the Philippines and has been submitted for regulatory authorization in multiple markets globally. NanoFlu, the company's quadrivalent influenza nanoparticle vaccine, met all primary objectives in its pivotal Phase 3 clinical trial in older adults. Novavax is currently evaluating a COVID-NanoFlu combination vaccine in a Phase 1/2 clinical trial, which combines the company's NVX-CoV2373 and NanoFlu vaccine candidates. These vaccine candidates incorporate Novavax' proprietary saponin-based Matrix-M adjuvant to enhance the immune response and stimulate high levels of neutralizing antibodies.

For more information, visitwww.novavax.comand connect with us on Twitter,LinkedIn, Instagram and Facebook.

Forward-Looking Statements

Statements herein relating to the future of Novavax, its operating plans and prospects, its partnerships, the ongoing development of NVX-CoV2373, the scope, timing and outcome of future regulatory filings and actions, Novavax' plans to submit a complete package to the U.S. FDA by the end of the year, and Novavax' plan to supplement the CMC data submitted to the MoHaP with data from the additional manufacturing sites in Novavax' global supply chain are forward-looking statements. Novavax cautions that these forward-looking statements are subject to numerous risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. These risks and uncertainties include challenges satisfying, alone or together with partners, various safety, efficacy, and product characterization requirements, including those related to process qualification and assay validation, necessary to satisfy applicable regulatory authorities; difficulty obtaining scarce raw materials and supplies; resource constraints, including human capital and manufacturing capacity, on the ability of Novavax to pursue planned regulatory pathways; challenges meeting contractual requirements under agreements with multiple commercial, governmental, and other entities; and those other risk factors identified in the "Risk Factors" and "Management's Discussion and Analysis of Financial Condition and Results of Operations" sections of Novavax' Annual Report on Form 10-K for the year ended December 31, 2020 and subsequent Quarterly Reports on Form 10-Q, as filed with the Securities and Exchange Commission (SEC). We caution investors not to place considerable reliance on forward-looking statements contained in this press release. You are encouraged to read our filings with the SEC, available at http://www.sec.gov and http://www.novavax.com, for a discussion of these and other risks and uncertainties. The forward-looking statements in this press release speak only as of the date of this document, and we undertake no obligation to update or revise any of the statements. Our business is subject to substantial risks and uncertainties, including those referenced above. Investors, potential investors, and others should give careful consideration to these risks and uncertainties.

Contacts:

Investors

Novavax, Inc.

Erika Schultz| 240-268-2022

ir@novavax.com

Solebury Trout

Alexandra Roy| 617-221-9197

aroy@soleburytrout.com

Media

Alison Chartan| 240-720-7804

Laura KeenanLindsey | 202-709-7521

media@novavax.com

Logo - https://mma.prnewswire.com/media/1506866/Novavax_High_Res_Logo.jpg

Go here to see the original:

Novavax Files for Emergency Use of COVID-19 Vaccine in the United Arab Emirates - KPVI News 6

Electrical and Behavioral Signals in OCD Could Guide Adaptive Therapy – Genetic Engineering & Biotechnology News

In an effort to improve treatment for obsessive compulsive disorder (OCD), researchers headed by teams at Brown University, and Baylor College of Medicine, have for the first time recorded electrical signals in the human brain that are associated with ebbs and flows in OCD symptoms, over an extended period, while individuals went about daily living in their homes. The research could be an important step in making an emerging therapy called deep brain stimulation (DBS) responsive to everyday changes in OCD symptoms.

In addition to advancing DBS therapy for cases of severe and treatment resistant OCD, this study has the potential for improving our understanding of the underlying neurocircuitry of the disorder, said Wayne Goodman, PhD, at Baylor College of Medicine. This deepened understanding may allow us to identify new anatomic targets for treatment that may be amenable to novel interventions that are less invasive than DBS. Goodman is co-author of the researchers published paper in Nature Medicine, which is titled, Long-term ecological assessment of intracranial electrophysiology synchronized to behavioural markers in obsessive-compulsive disorder.

OCD causes recurring unwanted thoughts and repetitive behaviors, and is a leading cause of disability. The condition, which is often debilitating, may affect perhaps 2-3% of the worlds population, the authors noted. Up to 20-40% of cases dont respond to traditional drug or behavioral treatments. Approximately 10% of individuals fail to achieve benefit from any intervention.

Deep brain stimulation, a technique that involves delivering mild electrical pulses via small electrodes precisely placed in the brain, can be effective in treating more than 50% of patients for whom other therapies failed. Over half of patients with treatment-resistant OCD are responders to DBS targeted to the ventral capsule/ventral striatum (VC/VS) region, the researchers further noted. To date, however, the number of patients who have received DBS for OCD is still in the hundreds.

One limitation of DBS is that it is unable to adjust to moment-to-moment changes in OCD symptoms, which are impacted by the physical and social environment. But adaptive DBS which can adjust the intensity of stimulation in response to real-time signals recorded in the braincould be more effective than traditional DBS and reduce unwanted side effects.

OCD is a disorder in which symptom severity is highly variable over time and can be elicited by triggers in the environment, said David Borton, PhD, an associate professor of biomedical engineering at Brown University, a biomedical engineer at the US Department of Veterans Affairs Center for Neurorestoration and Neurotechnology and a senior author of the new research. A DBS system that can adjust stimulation intensity in response to symptoms may provide more relief and fewer side effects for patients. But in order to enable that technology, we must first identify the biomarkers in the brain associated with OCD symptoms, and that is what we are working to do in this study. As the authors noted, An electrophysiological biomarker of symptom state would enable aDBS for OCD and other psychiatric disorders, which may provide a better approach for treating fluctuations in symptom intensity.

The research, led by Nicole Provenza, a recent Brown biomedical engineering PhD graduate from Bortons laboratory, was a collaboration between Bortons research group, affiliated with Browns Carney Institute for Brain Science and School of Engineering; the research groups of Wayne Goodman PhD, and Sameer Sheth MD, PhD, at Baylor College of Medicine; and Jeff Cohn, PhD, from the University of Pittsburghs Department of Psychology and Intelligent Systems Program and Carnegie Mellon University.

For their study, Goodmans team recruited five participants with severe OCD who were eligible for DBS treatment. Sheth, lead neurosurgeon, implanted in each participant an investigational DBS device from Medtronic, which is capable of both delivering stimulation and recording native electrical brain signals. Using the sensing capabilities of the hardware, the team gathered brain-signal data from participants in both clinical settings and at home as they went about daily activities. The DBS implants used in our study allow for real-time frequency-domain analysis of electrophysiological activity recorded simultaneously during stimulation delivery from the implanted electrodes, they wrote.

Along with the brain signal data, the team also collected a suite of behavioral biomarkers. In the clinical setting, these included facial expression (automatic facial affect recognition; AFAR) and body movement. Using computer vision and machine learning, they discovered that the behavioral features were associated with changes in internal brain states. At the participants homes, the team measured self-reports of OCD symptom intensity as well as biometric dataheart rate and general activity levelsrecorded by a smart watch and paired smartphone application, provided by Rune Labs. All of those behavioral measures were then time-synched to the brain-sensing data, enabling the researchers to look for correlations between the two.

Here, we acquired electrophysiological data with behavioral readouts over both short and long timescales, the team commented. In the clinic, we examined changes in affect (AFAR) during DBS parameter changes over short timescales (seconds to minutes). At home during participant-controlled recordings, we captured behavioral changes (self-reported OCD symptoms) over longer timescales (days to weeks to months) in natural settings, collected continuous data during natural and planned exposures, and developed methods to synchronize behavioral metrics to intracranial electrophysiology.

This is the first time brain signals from participants with neuropsychiatric illness have been recorded chronically at home alongside relevant behavioral measures, Provenza said. Using these brain signals, we may be able to differentiate between when someone is experiencing OCD symptoms, and when they are not, and this technique made it possible to record this diversity of behavior and brain activity.

Provenzas analysis of the data showed that the strategy did pick out brain-signal patterns potentially linked to OCD symptom fluctuation. While more work needs to be done across a larger cohort, this initial study shows that this technique is a promising way forward in confirming candidate biomarkers of OCD. we demonstrated the utility of at-home data collection for biomarker identification by observing correlations between spectral power and self-reported OCD symptom intensity.

We were able to collect a far richer dataset than has been collected before, and we found some tantalizing trends that wed like to explore in a larger cohort of patients, Borton said. Now we know that we have the toolset to nail down control signals that could be used to adjust stimulation level according to peoples symptoms.

Once those biomarkers are positively identified, they could then be used in an adaptive DBS system. Currently, DBS systems employ a constant level of stimulation, which can be adjusted by a clinician at clinical visits. Adaptive DBS systems, in contrast, would stimulate and record brain activity and behavior continuously without the need to attend clinic. When the system detects signals associated with an increase in symptom severity, it could ramp up stimulation to potentially provide additional relief. Likewise, stimulation could be toned down when symptoms abate. Such a system could potentially improve DBS therapy while reducing side effects.

Work on this line of research is ongoing. Because OCD is a complex disorder than manifests itself in highly variable ways across patients, the team hopes to expand the number of participants to capture more of that variability. They seek to identify a fuller set of OCD biomarkers that could be used to guide adaptive DBS systems. Once those biomarkers are in place, the team hopes to work with device makers to implement their DBS devices.

Our goal is to understand what those brain recordings are telling us and to train the device to recognize certain patterns associated with specific symptoms, Sheth said. The better we understand the neural signatures of health and disease, the greater our chances of using DBS to successfully treat challenging brain disorders like OCD. As the authors concluded, This work demonstrates the feasibility and utility of capturing chronic intracranial electrophysiology during daily symptom fluctuations to enable neural biomarker identification, a prerequisite for future development of adaptive DBS for OCD and other psychiatric disorders, the author concluded. The platform presented here lays the groundwork for future transformational studies reliant on ecological neural and behavioral monitoring and assessment of neuropsychiatric illness.

Read the original post:

Electrical and Behavioral Signals in OCD Could Guide Adaptive Therapy - Genetic Engineering & Biotechnology News

Gene Network Changes Associated with Cancer Onset and Progression Identify New Candidates for Targeted Gene Therapy | Research – Research Horizons

Cancer chemotherapy has undergone a paradigm shift in recent years with traditional treatments like broad-spectrum cytotoxic agents being complemented or replaced by drugs that target specific genes believed to drive the onset and progression of the disease.

This more personalized approach to chemotherapy became possible when genomic profiling of individual patient tumors led researchers to identify specific "cancer driver genes" that, when mutated or abnormally expressed, led to the onset and development of cancer.

Different types of cancer like lung cancer versus breast cancer and, to some extent, different patients diagnosed with the same cancer type show variations in the cancer driver genes believed to be responsible for disease onset and progression. For example, the therapeutic drug Herceptin is commonly used to treat breast cancer patients when its target gene, HER-2, is found to be over-expressed, says John F. McDonald, professor in the School of Biological Sciences.

McDonald explains that, currently, the identification of potential targets for gene therapy relies almost exclusively on genomic analyses of tumors that identify cancer driver genes that are significantly over-expressed.

But in their latest study, McDonald and Bioinformatics Ph.D. student Zainab Arshad have found that another important class of genetic changes may be happening in places where scientists dont normally look: the network of gene-gene interactions associated with cancer onset and progression.

Genes and the proteins they encode do not operate in isolation from one another, McDonald says. Rather, they communicate with one another in a highly integrated network of interactions.

What I think is most remarkable about our findings is that the vast majority of changes more than 90% in the network of interactions accompanying cancer are not associated with genes displaying changes in their expression, adds Arshad, co-author of the paper. What this means is that genes playing a central role in bringing about changes in network structure associated with cancer the hub genes may be important new targets for gene therapy that can go undetected by gene expression analyses.

Their research paper Changes in gene-gene interactions associated with cancer onset and progression are largely independent of changes in gene expression is published in the journal iScience.

Mutations, expression and changes in network structure

In the study, Arshad and McDonald worked with samples of brain, thyroid, breast, lung adenocarcinoma, lung squamous cell carcinoma, skin, kidney, ovarian, and acute myeloid leukemia cancers and they noticed differences in cell network structure for each of these cancers as they progressed from early to later stages.

When early-stage cancers develop, and stayed confined to their body tissue of origin, they noted a reduction in network complexity relative to normal pre-cursor cells. Normal, healthy cells are highly differentiated, but as they transition to cancer, [T]hey go through a process of de-differentiation to a more primitive or stem cell-like state. Its known from developmental biology that as cells transition from early embryonic stem cells to highly specialized fully differentiated cells, network complexity increases. What we see in the transition from normal to early-stage cancers is a reversal of this process, McDonald explains.

McDonald says as the cancers progress to advanced stages, when they can spread or metastasize to other parts of the body, [W]e observe re-establishment of high levels of network complexity, but the genes comprising the complex networks associated with advanced cancers are quite different from those comprising the complex networks associated with the precursor normal tissues.

As cancers evolve in function, they are typically associated with changes in DNA structure, and/or with changes in the RNA expression of cancer driver genes. Our results indicate that theres an important third class of changes going on changes in gene interactions and many of these changes are not detectable if all youre looking for are changes in gene expression.

DOI:https://doi.org/10.1016/j.isci.2021.103522

Acknowledgments: This research was supported by the Mark Light Integrated Cancer Research Center Student Fellowship , the Deborah Nash Endowment Fund , and the Ovarian Cancer Institute (Atlanta), where John F. McDonald serves as chief research officer. The results shown here are based upon data generated by the TCGA Research Network: http://cancergenome.nih.gov/.

About Georgia Institute of Technology

The Georgia Institute of Technology, or Georgia Tech, is a top 10 public research university developing leaders who advance technology and improve the human condition. The Institute offers business, computing, design, engineering, liberal arts, and sciences degrees. Its nearly 40,000 students representing 50 states and 149 countries, study at the main campus in Atlanta, at campuses in France and China, and through distance and online learning. As a leading technological university, Georgia Tech is an engine of economic development for Georgia, the Southeast, and the nation, conducting more than $1 billion in research annually for government, industry, and society.

See the rest here:

Gene Network Changes Associated with Cancer Onset and Progression Identify New Candidates for Targeted Gene Therapy | Research - Research Horizons

Researchers ‘turn off’ driver of aortic stenosis heart disease | Cornell Chronicle – Cornell Chronicle

Researchers have discovered how to turn off a key driver of aortic stenosis the narrowing of the hearts aortic valve identifying for the first time the biological process behind certain instances of the disease in which heart valves become calcified and damaged.

The research was reported Nov. 5 in Science Advances, and the breakthrough was over a decade in the making for the studys co-author Jonathan Butcher, professor of biomedical engineering.

Since 2009, Butcher has been studying cells essential for embryonic development of the cardiovascular system. Wanting to show what a subset of those cells would do in a disease state, he published a 2012 study finding that a specific type of inflammation can trigger the cells to undergo the same biological process as they do in the development stage.

Developmental biology used to be studied completely separate from adult disease because they were seen as driving two completely different systems, Butcher said. More recently, theres been the idea that molecules that drive tissue formation might also be involved in forming a tissue-level response to an external stimulus like a disease.

In the case of the cells responsible for heart valve development and disease, Butcher wanted to know more about their shared regulatory component.

Butcher was presenting his work at a research consortium in which another researcher, Michel Puceat from Aix-Marseille University, shared research on a natural biological program in adult mouse heart valves known as OCT4, which Butcher recognized as an early development program and was surprised to see in adult subjects.

The researchers agreed to work together, doing molecular gain and loss of function studies to show that OCT4 switches off very early in embryonic development, but can be turned on later in adulthood. What flips the switch is the inflammatory transcription factor NF kappa B the same one Butcher had studied a decade ago but this time, the OCT4 program was operating a different lineage of cells.

We found this nascent ability of the cells to form bone thats suppressed in the embryonic environment, Butcher said, but in the adult disease environment, its now amplifying that nascent desire to become an osteochondral progenitor.

Essentially, inflammation can switch on dormant embryonic programming in adult cells, and the disease environment leads them to behave differently and calcify the heart valve, causing aortic stenosis.

For the last portion of the study, the researchers wanted to see if they could prevent stenosis in mice by genetically deactivating the OCT4 program after its embryonic role was finished. The experiment was successful, and mice with OCT4 deleted in pro-valve tissue resisted the disease despite having the genetic risk factor and a high-fat, inflammation-inducing diet.

The difference was remarkable and it suggests this particular mechanism could be a pretty safe way to treat the disease because you're not going to worry about disrupting a whole bunch of other things, said Butcher, who added that there are several options for exploring a therapy for humans. We might be able to block it with anti-inflammatory drugs that stop the switch operator, or it might be safer to block it by manipulating this transformation component downstream.

Butcher said the research is an example of observing and targeting emergent phenomena by going beyond the traditional method of studying individual cells and molecules as disease drivers, and instead observing the relationships between components.

This particular work to me was something that really engaged the ingenuity of a lot of people, Butcher said. This concept of emergence will be critically important for developing next-level therapy for diseases.

The research was funded by the Leducq Foundation, the National Institutes of Health and the National Science Foundation.

Syl Kacapyr is public relations and content manager for the College of Engineering.

Read more:

Researchers 'turn off' driver of aortic stenosis heart disease | Cornell Chronicle - Cornell Chronicle

Fate Therapeutics Showcases Positive Interim Phase 1 Data from FT596 Off-the-shelf, … – The Bakersfield Californian

5 of 6 Patients Achieve Objective Response, including 4 Patients with Complete Response, with Single Dose of FT596 at 900 Million Cells in Combination with Rituximab

13 of 19 Patients Achieve Objective Response with Single Dose of FT596 at 90 Million and 300 Million Cell Dose; 10 of 11 Patients Treated with a Second FT596 Cycle Continue in Ongoing Response, with 3 Patients in Ongoing Complete Response at 6 Months Follow-up; Additional 2 Patients Reach 6 Months in Complete Response

FT596 Treatment Regimens were Well-tolerated; No Dose-limiting Toxicities, and No Adverse Events of Any Grade of ICANS or GVHD, were Observed; Three Low-grade Adverse Events of CRS Resolved without Intensive Care Treatment

Company to Host Virtual Investor Event Tomorrow at 8:00 AM Eastern Time

SAN DIEGO, Dec. 13, 2021 (GLOBE NEWSWIRE) -- Fate Therapeutics, Inc. (NASDAQ: FATE), a clinical-stage biopharmaceutical company dedicated to the development of programmed cellular immunotherapies for cancer, today showcased positive interim Phase 1 data from the Companys FT596 program for patients with relapsed / refractory B-cell lymphoma (BCL) at the 63rd American Society of Hematology (ASH) Annual Meeting and Exposition. FT596 is the Companys off-the-shelf, multi-antigen targeted, iPSC-derived natural killer (NK) cell product candidate derived from a clonal master induced pluripotent stem cell (iPSC) line engineered with three anti-tumor functional modalities: a proprietary chimeric antigen receptor (CAR) optimized for NK cell biology that targets B-cell antigen CD19; a novel high-affinity, non-cleavable CD16 (hnCD16) Fc receptor that has been modified to prevent its down-regulation and to enhance its binding to tumor-targeting antibodies; and an IL-15 receptor fusion (IL-15RF) that augments NK cell activity.

The interim dose-escalation clinical data from our FT596 program in relapsed / refractory B-cell lymphoma demonstrate that off-the-shelf, iPSC-derived CAR NK cells can bring substantial therapeutic benefit to heavily pre-treated patients in urgent need of therapy, with high response rates and meaningful duration of responses, said Scott Wolchko, President and Chief Executive Officer of Fate Therapeutics. We are particularly pleased with the therapeutic profile that has emerged with FT596 in combination with rituximab, where over half of the patients treated with a single dose of FT596 at higher dose levels achieved a complete response with a favorable safety profile that is clearly differentiated from CAR T-cell therapy. We look forward to assessing a two-dose treatment schedule for FT596 to further define its potential best-in-class therapeutic profile and ability to reach more patients, including those earlier in care.

The ongoing Phase 1 study in relapsed / refractory BCL is assessing a single dose of FT596 as monotherapy (Monotherapy Arm) and in combination with a single dose of rituximab (375 mg/m2) (Combination Arm) following three days of conditioning chemotherapy (500 mg/m2 of cyclophosphamide and 30 mg/m2 of fludarabine). Certain patients are eligible for re-treatment with a second, single-dose cycle.

The ASH presentation ( Session 704Cellular Immunotherapies: Expanding Targets and Cellular Sources for Immunotherapies, Abstract 823 ) includes clinical data from 25 evaluable patients for safety (n=12 in Monotherapy Arm; n=13 in Combination Arm) in the first, second, and third single-dose cohorts of 30 million, 90 million, and 300 million cells, respectively, of which 24 patients were also evaluable for efficacy (n=12 in Monotherapy Arm; n=12 in Combination Arm), as of the data cutoff date of October 11, 2021. These 25 patients had received a median of four prior lines of therapy and a median of two prior lines containing CD20-targeted therapy. Of the 25 patients, 15 patients (60%) had aggressive B-cell lymphoma, 15 patients (60%) were refractory to most recent prior therapy, and 8 patients (32%) were previously treated with autologous CD19-targeted CAR T-cell therapy. Subsequent to the data cutoff date for the ASH presentation, an additional patient in the third single-dose cohort of the Combination Arm was evaluable for initial anti-tumor response, and seven patients in the fourth single-dose cohort of 900 million cells (n=1 in Monotherapy Arm; n=6 in Combination Arm) were evaluable for safety and initial anti-tumor response.

Single-dose, Single-cycle Response Data

In the second, third, and fourth dose cohorts of the Monotherapy and Combination Arms comprising a total of 26 patients, 18 patients (69%) achieved an objective response, including 12 patients (46%) that achieved a complete response, on Day 29 following a single dose of FT596 (see Table 1). Nine of these 26 patients were previously treated with autologous CD19-targeted CAR T-cell therapy and, of these nine patients, six achieved an objective response (67%) on Day 29 following a single dose of FT596. Notably, in the third and fourth dose cohorts of the Combination Arm comprising a total of 12 patients, nine patients (75%) achieved an objective response, including seven patients (58%) that achieved a complete response, on Day 29 following a single dose of FT596.

Durability of Response Data

The ASH presentation includes durability of response data from 13 responding patients in the second and third single-dose cohorts of 90 million cells and 300 million cells (n=9 in Monotherapy Arm; n=10 in Combination Arm). As of the data cutoff date of October 11, 2021, 10 patients continued in ongoing response, including three patients in ongoing complete response at least six months from initiation of treatment; two patients reached six months in complete response and subsequently had disease progression; and one patient had disease progression prior to six months. Of these 13 responding patients:

Monotherapy Arm (n=7 responding patients). Five patients, all of whom were treated with a second FT596 single-dose cycle with the consent of the U.S. Food and Drug Administration (FDA), continued in ongoing response at a median follow-up of 4.1 months, including one patient in ongoing complete response at 8.1 months; one patient, who was treated with only one FT596 single-dose cycle, reached six months in complete response and subsequently had disease progression at 6.5 months; and one patient, who was treated with only one FT596 single-dose cycle, had disease progression at 1.7 months.Combination Arm (n=6 responding patients). Five patients, all of whom were treated with a second FT596 single-dose cycle with the consent of the FDA, continued in ongoing response at a median follow-up of 4.6 months, including two patients in ongoing complete response at 6.0 and 10.8 months; and one patient, who was treated with a second FT596 single-dose cycle with the consent of the FDA, reached six months in complete response and subsequently had disease progression at 6.7 months.

aCD19 = autologous CD19-targeted CAR T-cell therapy; Aggressive = diffuse large B-cell lymphoma, Grade 3b follicular lymphoma, Richters transformation, and high-grade B-cell lymphoma; CR = complete response; Indolent = splenic diffuse red pulp small B-cell lymphoma, non-Grade 3b follicular lymphoma, Waldenstroms macroglobulinemia, and small lymphocytic lymphoma; M = million; OR = objective response 1 As of data cutoff date of October 11, 2021, unless otherwise noted. Objective response and complete response are based on Cycle 1 Day 29 protocol-defined response assessment per Lugano 2014 criteria. Data subject to source document verification. 2 Cycle 1 Day 29 protocol-defined response assessment completed subsequent to data cutoff date for one patient in the third single-dose cohort of 300 million cells in the Combination Arm and seven patients in the fourth single-dose cohort of 900 million cells (n=1 in Monotherapy Arm; n=6 in Combination Arm).

Safety Data

The FT596 treatment regimens were well tolerated, including in those patients treated with a second, single-dose cycle. No dose-limiting toxicities, and no treatment-emergent adverse events (TEAEs) of any grade of immune effector cell-associated neurotoxicity syndrome (ICANS) or graft-versus-host disease (GvHD) were observed. Three low-grade adverse events (two Grade 1, one Grade 2) of cytokine release syndrome (CRS) were reported, which were of limited duration and resolved without intensive care treatment (see Table 2).

The Company has initiated enrollment of a two-dose treatment schedule in the Combination Arm, with FT596 administered on Day 1 and Day 15 at 900 million cells per dose. Patients with clinical benefit following administration of the first two-dose cycle are eligible for re-treatment with a second two-dose cycle. Additionally, patients with clinical response are eligible for re-treatment following disease progression.

CRS = Cytokine Release Syndrome; GvHD = Graft vs. Host Disease; ICANS = Immune Cell-Associated Neurotoxicity Syndrome; TEAE = Treatment-Emergent Adverse Event; SAE = Severe Adverse Events a Grade 2 CRS

Investor Event Webcast

The Company will host a live audio webcast on Tuesday, December 14, 2021 at 8:00 a.m. ET to highlight interim Phase 1 clinical data from the Companys FT516 and FT596 programs for the treatment of relapsed / refractory B-cell lymphoma. The live webcast can be accessed under "Events & Presentations" in the Investors section of the Company's website at http://www.fatetherapeutics.com. The archived webcast will be available on the Company's website beginning approximately two hours after the event.

About Fate Therapeutics iPSC Product Platform The Companys proprietary induced pluripotent stem cell (iPSC) product platform enables mass production of off-the-shelf, engineered, homogeneous cell products that are designed to be administered with multiple doses to deliver more effective pharmacologic activity, including in combination with other cancer treatments. Human iPSCs possess the unique dual properties of unlimited self-renewal and differentiation potential into all cell types of the body. The Companys first-of-kind approach involves engineering human iPSCs in a one-time genetic modification event and selecting a single engineered iPSC for maintenance as a clonal master iPSC line. Analogous to master cell lines used to manufacture biopharmaceutical drug products such as monoclonal antibodies, clonal master iPSC lines are a renewable source for manufacturing cell therapy products which are well-defined and uniform in composition, can be mass produced at significant scale in a cost-effective manner, and can be delivered off-the-shelf for patient treatment. As a result, the Companys platform is uniquely designed to overcome numerous limitations associated with the production of cell therapies using patient- or donor-sourced cells, which is logistically complex and expensive and is subject to batch-to-batch and cell-to-cell variability that can affect clinical safety and efficacy. Fate Therapeutics iPSC product platform is supported by an intellectual property portfolio of over 350 issued patents and 150 pending patent applications.

About FT596 FT596 is an investigational, universal, off-the-shelf natural killer (NK) cell cancer immunotherapy derived from a clonal master induced pluripotent stem cell (iPSC) line engineered with three anti-tumor functional modalities: a proprietary chimeric antigen receptor (CAR) optimized for NK cell biology that targets B-cell antigen CD19; a novel high-affinity 158V, non-cleavable CD16 (hnCD16) Fc receptor, which has been modified to prevent its down-regulation and to enhance its binding to tumor-targeting antibodies; and an IL-15 receptor fusion (IL-15RF) that augments NK cell activity. In preclinical studies of FT596, the Company has demonstrated that dual activation of the CAR19 and hnCD16 targeting receptors enhances cytotoxic activity, indicating that multi-antigen engagement may elicit a deeper and more durable response. Additionally, in a humanized mouse model of lymphoma, FT596 in combination with the anti-CD20 monoclonal antibody rituximab showed enhanced killing of tumor cells in vivo as compared to rituximab alone. FT596 is being investigated in a multi-center Phase 1 clinical trial for the treatment of relapsed / refractory B-cell lymphoma as a monotherapy and in combination with rituximab, and for the treatment of relapsed / refractory chronic lymphocytic leukemia (CLL) as a monotherapy and in combination with obinutuzumab (NCT04245722).

About Fate Therapeutics, Inc. Fate Therapeutics is a clinical-stage biopharmaceutical company dedicated to the development of first-in-class cellular immunotherapies for patients with cancer. The Company has established a leadership position in the clinical development and manufacture of universal, off-the-shelf cell products using its proprietary induced pluripotent stem cell (iPSC) product platform. The Companys immuno-oncology pipeline includes off-the-shelf, iPSC-derived natural killer (NK) cell and T-cell product candidates, which are designed to synergize with well-established cancer therapies, including immune checkpoint inhibitors and monoclonal antibodies, and to target tumor-associated antigens using chimeric antigen receptors (CARs). Fate Therapeutics is headquartered in San Diego, CA. For more information, please visit http://www.fatetherapeutics.com.

Forward-Looking Statements This release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995 including statements regarding the safety and therapeutic potential of the Companys iPSC-derived NK cell product candidates, including FT596, its ongoing and planned clinical studies, and the expected clinical development plans for FT596. These and any other forward-looking statements in this release are based on management's current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to, the risk that results observed in studies of its product candidates, including preclinical studies and clinical trials of any of its product candidates, will not be observed in ongoing or future studies involving these product candidates, the risk that the Company may cease or delay clinical development of any of its product candidates for a variety of reasons (including requirements that may be imposed by regulatory authorities on the initiation or conduct of clinical trials, the amount and type of data to be generated, or otherwise to support regulatory approval, difficulties or delays in subject enrollment and continuation in current and planned clinical trials, difficulties in manufacturing or supplying the Companys product candidates for clinical testing, and any adverse events or other negative results that may be observed during preclinical or clinical development), and the risk that its product candidates may not produce therapeutic benefits or may cause other unanticipated adverse effects. For a discussion of other risks and uncertainties, and other important factors, any of which could cause the Companys actual results to differ from those contained in the forward-looking statements, see the risks and uncertainties detailed in the Companys periodic filings with the Securities and Exchange Commission, including but not limited to the Companys most recently filed periodic report, and from time to time in the Companys press releases and other investor communications.Fate Therapeutics is providing the information in this release as of this date and does not undertake any obligation to update any forward-looking statements contained in this release as a result of new information, future events or otherwise.

Contact: Christina Tartaglia Stern Investor Relations, Inc. 212.362.1200 christina@sternir.com

Go here to see the original:

Fate Therapeutics Showcases Positive Interim Phase 1 Data from FT596 Off-the-shelf, ... - The Bakersfield Californian

ACT Party’s boycott of RNZ’s Morning Report caused by host …

The term 'eugenics' refers to the selection of desired heritable characteristics in order to improve future generations, and is often associated with Nazi Germany.

Morton's complaint against RNZ over the comment was not upheld. The BSA in April 2021 found no breaches of its guidelines for Good Taste and Decency, Balance, Accuracy or Fairness, and said the ACT Party was "treated fairly in the context of the debate".

But Morton told Newshub on Thursday the comment was the final straw for the party, and since then, no ACT MPs have appeared in live interviews for the show.

Newshub has reached out to RNZ for comment.

The boycott first came to light on Thursday morning, after The Spinoff published an interview with Seymour in which he described Morning Report as rude, selective and dishonest about what they wanted to talk about.

"After the umpteenth time that I went on their show out of a feeling of public duty and was belittled and abused with all their snarkiness, I just thought, 'I don't need this,'" he said.

But he told The Spinoff that the "really toxic and comically Lilliputian culture of Morning Report" was different from the rest of RNZ, and ACT MPs would happily appear on the station's other shows.

Morton told Newshub ACT MPs still also appear in pre-recorded interviews that are played as part of Morning Report's news bulletins.

While Seymour was happy for his party to ditch Morning Report, he decried Jacinda Ardern's decision to do much the same thing earlier this year, when she pulled out of her weekly slot on Newstalk ZB's Mike Hosking Breakfast show.

He said in March the Prime Minister was avoiding answering questions by "de-platforming" herself from the weekly slot.

"Jacinda Ardern will ultimately regret this escalating arrogance, the latest example being cancelling her weekly discussion with Newstalk ZB's Mike Hosking," Seymour said.

"It joins a long list of increasingly hubristic moves from the Prime Minister and her Government."

Ardern said the decision was made so she could branch out more to other media outlets, but broadcaster Hosking said in March that Ardern was "running for the hills" and was "over being held to account".

He said he didn't want Ardern back on his show after she cancelled the slot, which had been observed by New Zealand Prime Ministers for more than 30 years.

Often critical of the Government, Hosking said late last year people "misunderstand" his relationship with Ardern and despite often fiery interviews, he actually "likes her a lot".

"It's our work," Hosking said in December. "It's what we do. There's nothing personal in it."

Read more:

ACT Party's boycott of RNZ's Morning Report caused by host ...

Letter: Pay attention to facts – The Columbian

I am glad readers are somewhat perusing my letters. Lets pay attention to facts and details.

A recent letter substituted progressives to Democrats (historically correct) with a bold assertion that Democrats nor the left support eugenics, abortion or cultural cleansing. Those were progressive pursuits. But, when reading the Democratic Party platform, one will read these words: that every woman should be able to access high-quality reproductive health care services, including safe and legal abortion. Again, corroborate what you know or believe.

This verification unequivocally refutes the claim that the Democrats and the left do not support abortions specifically. Do readers follow voting records of politicians or actions of the Department of Justice that the current administration advocate? Should the Democratic Party platform be denounced?

Another rebuttal is necessary. The major increase in crime during the Trump administration occurred largely in states and cities that are Democratic bastions wholly under their jurisdictions. President Trump honored the Ninth and 10th amendments. Crime and civil violence are escalating under this current administration. Can these points be refuted? No. Be cognizant of what is going on in Portland, Seattle, San Francisco, and more.

Go here to see the original:

Letter: Pay attention to facts - The Columbian

Bioethicists Okay Human Extinction to Eliminate Suffering – National Review

(solarseven/iStock/Getty Images)

These days, anti-humanism is as thick as molasses among the intelligentsia. That includes an ongoing conversation in bioethics whether all things considered human extinction would be a fine thing because of the suffering that never coming into existence would avoid.

Example: A few months ago, Oxford professor Roger Crisp opined that we might not want to stop a huge asteroid from hitting the Earth. From Would extinction be so bad?:

Consider the huge amount of suffering that continuing existence will bring with it, not only for humans, and perhaps even for post-humans, but also for sentient non-humans, who vastly outnumber us and almost certainly would continue to do so. As far as humans alone are concerned, Hilary Greaves and Will MacAskill at the University of Oxfords Global Priorities Institute estimate that there could beone quadrillion(1015) people to come an estimate they describe as conservative.

These numbers, and the scale of suffering to be put into the balance alongside the good elements in individuals lives, are difficult to fathom and so large that its not obvious that you should deflect the asteroid. In fact, there seem to be some reasons to think you shouldnt.

Perhaps one reason we think extinction would be so bad is that we have failed to recognise just how awful extreme agony is. Nevertheless, we have enough evidence, and imaginative capacity, to say that it is not unreasonable to see the pain of an hour of torture as something that can never be counterbalanced by any amount of positive value. And if this view is correct, then it suggests that the best outcome would be the immediate extinction that follows from allowing an asteroid to hit our planet.

Crisp equivocates a bit at the end, writing, I am not claiming that extinction wouldbe good;only that, since itmight be, we should devote a lot more attention to thinking about the value of extinction than we have to date. Good grief. Is the issue really debatable?

Not to be outdone, writing in response to Crisp in the Journal of Medical Ethics Blog, University of Calgary professor Walter Glannon shrugs his big brain at the prospect of us being gone. From A world without us:

We cannot predict the sort of lives future people would have because we do not know the sort of world they would inhabit. But the circumstances described above make it difficult to be optimistic. Regardless of the hypothetical value or disvalue of these lives, possible people are not deprived of anything if they do not come into existence.

We have an obligation to collectively act to prevent or reduce the suffering that present and future humans will actually experience. This depends on controlling natural habitats, deforestation, carbon emissions and other processes. Future actual people have the same rights and interests in avoiding suffering as present actual people. The extent of suffering may provide a pro tanto reason to prevent them from existing. Even if there is no such reason, merely possible people do not have these rights and interests because they do not and will not exist. If we become extinct, then the world will go on without us and will be good or bad for no one.

Why do ivory-tower discussions like this matter? Because these nihilists are teaching the society leaders of tomorrow, those who will exert tremendous influence over future public policies and cultural attitudes. With our supposedly best minds suggesting that human extinction could be desirable, is it any wonder why so many of our young people seem to be despairing?

Moreover, the utter terror of suffering is pathological and leads directly to evil and/or terribly wrongheaded utilitarian policies such as eugenics and social Darwinism. It is also the moving force behind the euthanasia movement, which seeks to eliminate suffering by eliminating the sufferer. Avoiding suffering is also the central philosophical core of the transhumanism quasi-religion, which seeks to create a corporeal immortality by instilling a new eugenics with very sharp teeth.

So, what should be our attitude toward suffering? It should not be utopian scheming. Nor, to be sure, should it be indifference. Rather, we have a human duty to mitigate each others suffering, to love and suffer with each other which is the root meaning of compassion. And we can harness our own suffering to grow and become better individuals.

In this regard, for my Humanize podcast, I recently interviewed the quadriplegic Christian evangelist and disability rights activists Joni Eareckson Tada, who unexpectedly took a deep dive into this very issue, and in a very intimate and personal way. Regardless of faith issues, her attitude toward and personal response to her own deep suffering is much healthier than the nihilism that has grown so dark within utilitarian bioethics that some dont reject the prospect of human extinction out of hand.

More:

Bioethicists Okay Human Extinction to Eliminate Suffering - National Review

ACT Party’s boycott of RNZ’s Morning Report caused by host comparing one of its policies to eugenics – Newshub

The term 'eugenics' refers to the selection of desired heritable characteristics in order to improve future generations, and is often associated with Nazi Germany.

Morton's complaint against RNZ over the comment was not upheld. The BSA in April 2021 found no breaches of its guidelines for Good Taste and Decency, Balance, Accuracy or Fairness, and said the ACT Party was "treated fairly in the context of the debate".

But Morton told Newshub on Thursday the comment was the final straw for the party, and since then, no ACT MPs have appeared in live interviews for the show.

Newshub has reached out to RNZ for comment.

The boycott first came to light on Thursday morning, after The Spinoff published an interview with Seymour in which he described Morning Report as rude, selective and dishonest about what they wanted to talk about.

"After the umpteenth time that I went on their show out of a feeling of public duty and was belittled and abused with all their snarkiness, I just thought, 'I don't need this,'" he said.

But he told The Spinoff that the "really toxic and comically Lilliputian culture of Morning Report" was different from the rest of RNZ, and ACT MPs would happily appear on the station's other shows.

Morton told Newshub ACT MPs still also appear in pre-recorded interviews that are played as part of Morning Report's news bulletins.

While Seymour was happy for his party to ditch Morning Report, he decried Jacinda Ardern's decision to do much the same thing earlier this year, when she pulled out of her weekly slot on Newstalk ZB's Mike Hosking Breakfast show.

He said in March the Prime Minister was avoiding answering questions by "de-platforming" herself from the weekly slot.

"Jacinda Ardern will ultimately regret this escalating arrogance, the latest example being cancelling her weekly discussion with Newstalk ZB's Mike Hosking," Seymour said.

"It joins a long list of increasingly hubristic moves from the Prime Minister and her Government."

Ardern said the decision was made so she could branch out more to other media outlets, but broadcaster Hosking said in March that Ardern was "running for the hills" and was "over being held to account".

He said he didn't want Ardern back on his show after she cancelled the slot, which had been observed by New Zealand Prime Ministers for more than 30 years.

Often critical of the Government, Hosking said late last year people "misunderstand" his relationship with Ardern and despite often fiery interviews, he actually "likes her a lot".

"It's our work," Hosking said in December. "It's what we do. There's nothing personal in it."

Read this article:

ACT Party's boycott of RNZ's Morning Report caused by host comparing one of its policies to eugenics - Newshub

Why we shouldn’t glorify Lord of the Rings – The Spinoff

Peter Jacksons trilogy has been loved by New Zealand for 20 years. Naomii Seah asks if its time we take a closer look.

Lord of the Rings is meticulously crafted, beautifully shot and visionary. The project pioneered visual effects techniques and camera work, employed over 20,000 people in New Zealand alone, and has boosted our national revenue through tourism and merchandise.

But I still dont like it.

Why? Well, for one I have the attention span of a gnat, and more than three hours per movie is just too much. But thats my own fault for watching too many TikToks.

Jokes aside, JRR Tolkien, although in many ways progressive for his time, was not immune to the rhetoric of eugenics and imperialism that permeated Britain in the early-mid 20th century. Theres been endless debate about whether Tolkien was racist. I dont care about that. But he was a British citizen, writing around the time of World War II. And it shows in his description of Orcs as squat, broad, flat-nosed, sallow-skinned, with wide mouths and slant eyes: in fact degraded and repulsive versions of the (to Europeans) least lovely Mongol-types. Its also evident in the way Orc-Goblins and Orc-Men are considered monstrous: an unpleasant echo of the mid-20th-century eugenics movement, which sought to prevent inter-ethnic marriages. Genetic determinism is also front and centre in Middle-Earth, driving its central conflict.

For a film that began production in 1997, Jackson and co sure did carry over a lot of that 1950s prejudice.

Twenty years ago may seem like a long time. Times were different in the early 2000s! I hear you yell across the internet abyss. But it had been an even longer time between the publication of The Fellowship of the Ring in 1954 and Jacksons film.

Between 1954 and 1997, apartheid and the civil rights movement had brought global attention to systemic racism. Locally, the 1970s and 80s saw an era dubbed the Mori renaissance, where indigenous arts and language flourished, as those whod had their culture beaten out of them began to reclaim their whakapapa.

Increasing indigenous activism saw a rebrand of New Zealand as a bicultural nation, and perceptions of race relations between Mori and Pkeh continued to be seen positively overseas, despite the realities of day-to-day life.

And in the midst of this swirling debate about race relations, biculturalism and equity, Jackson created a white imperialist film?

Lets unpack. Tolkien aimed to create a sense of history with Middle-Earth. Tolkiens hobbits are meant to represent domestic middle-class England; a romanticised, pastoral, simple way of life that is long gone. Hobbits are ordinary folk and in Jacksons films, ordinary folk are exclusively white or at least white-passing.

That seems particularly damaging when one considers the films positioning as part of New Zealands national identity. Are all New Zealanders meant to identify with the (white) hobbits? Its a callback to the settler culture of New Zealand in the 20th century, when Pkeh glorified the motherland and anglophilia dominated the emerging culture.

Jackson himself noted that his vision of Middle-Earth is more like history than fantasy, and in his interpretation of the texts, Jackson has made it clear that his vision of history is white.

So where are all the people of colour in Jacksons Middle-Earth? Surprise! Theyre the bad guys. The screen adaptation takes the racial coding of Tolkiens description of the Orcs and supercharges it. In the films, Lawrence Makoare and Sala Baker two of the few cast members of colour played the villainous Uruk-hai captain Lurtz, and Sauron himself. Lurtzs White hand of Saruman bears disturbing resemblance to Aboriginal body art, and the facial piercings, darkened skin and dreadlocked hair of the evil races are all cultural markers of ethnic minorities.

While Tolkien at least attempts to humanise the Orcs in his novels, theres little such nuance in Jacksons films. Orcs are born bad, from literal mud and filth, and they oppose ordinary white people.

The central irony is the close association of free peoples and nature. Its a radically revisionist interpretation of history, considering colonisation decimated the landscape of Aotearoa. So it seems extra insidious that an English, and lets face it, white narrative, which explicitly labels the north and west good in opposition to the evil east and south, has become so deeply rooted in the national consciousness.

Its a beautiful film, and for New Zealand watchers, its particularly gratifying to see local scenes displayed in breathtaking panoramic shots. But Jacksons film is not set in New Zealand. And the conflation of Middle-Earth with its English values and imperial undertones with our post-colonial nation is a troubling one. Particularly when the film, and Jackson, are placed on such high pedestals.

But its time we had a closer look at our cultural narratives. Whos writing them? Whos funding it? (Spoiler, the New Zealand army helped build Hobbiton. Make of that what you will). What are their interests? And as a nation, arent we trying to move on from the atrocities of the colonial era?

So before anyone accuses me of being unpatriotic, let me finish by clearing the air. I dont hate Jacksons work. I hate what it stands for.

Were talking about elves, dwarves, cave trolls and sneaky little hobbitses for an entire week. Read the rest of our dedicated Lord of the Rings 20th anniversary coveragehere.

Excerpt from:

Why we shouldn't glorify Lord of the Rings - The Spinoff

Time Will Tell: Three Black Scholars Ponder APA’s Apology for Silence and Complicity in Perpetuating Racism – Diverse: Issues in Higher Education

Dr. Don Pope-DavisFrom the time children enter school until they graduate, they will take a myriad of psychological and achievement tests measuring their cognitive ability and/or their intelligence quotient (IQ). In America, psychological testing and assessments have increasingly become a prerequisite for many high-stakes competitions, college admissions and scholarships, as well as for entering our national workforce. Currently, there is little evidence of these efforts abating, even in the presence of complaints by those most damaged, harmed, stigmatized and further marginalized by tests minoritized, international, linguistically different, low-income individuals and people of color. The testing industry is prolific and is as engrained in our American experience as the proverbial apple pie.

The historical proliferation of these assessments was spurred in part by French schools in the early 1900s, as white psychologists and psychometricians began to develop early theories and conjectures of learning, and to simultaneously acquire initial beliefs of intelligence, which remain today. Those children who did not pass were deemed imbeciles and removed from classrooms. The genesis of the testing movement created many tests, including the Stanford-Binet Test, which subsequently has been administered to millions of American schoolchildren. Also, all immigrants who came to the United States in the early 20th century via Ellis Island were given the Feature Profile Test on American history. Those who did not pass the test were called feebleminded and frequently sent back home.

Problematically, intelligence, aptitude and achievement tests are still used with dismissiveness. This continues a legacy of blatant disregard for cultural, linguistic and environmental influences in childrens development, resulting in subsequent interpretations and uses of scores scores that often differ across racial, ethnic, linguistic and economic backgrounds. Social scientists like Herrnstein and Murray seized the moment in 1994 to capitalize on polemic, deficit-oriented and racist beliefs in their highly supported and highly contested book reminiscent of eugenics advocates.Dr. Donna Y. Ford

Within this context, the American Psychological Association (APA) recently issued a long-overdue apology for the harm the organization and its member psychologists have done in perpetuating systematic racism and its complicit role in exacerbating myths around racial hierarchies, particularly regarding Black communities. APA acknowledges its role in perpetuating racism under the guise of science and the faade of objectivity. The association now more directly proclaims that race is a social construct with no underlying genetic or biological basis.

As Black scholars and leaders in psychology, counseling and education, we strive to expose and mitigate barriers that regularly inhibit educational progress and outcomes for Black and other vulnerable groups. With this in mind, we challenge prevailing moral and social beliefs that permeate institutions. We endeavor to shape more reasonable and moral standards that address structural racism that has served to maintain the status quo.

The Association of Black Psychologists also issued a response. They concluded: To accept the APAs apology would be to accept the accuracy of a fabricated historical record and negate the mission and vision of the Association of Black Psychologists. To our disappointment, to date, responses from other professional organizations are noticeably absent. One exception is theAmerican Psychiatric Association.

Individuals and organizations should not be silent. Instead, we must speak truth to power and work in coalition toward a path forward, proactively and unapologetically grounded in anti-racism. The healing is in the pain. We believe that APA leadership, in collaboration with other organizations, should take a next step by establishing a Truth and Reconciliation Commission similar to South Africas in 1995. That commission helped accelerate the healing process in the aftermath of apartheid. This will take effort, but the urgency of now is upon us.

Regardless of APAs apologetic treatise, the lethal effects of oppressive psychological science still exist and remain an often-debilitating force in the lives of Blacks and other communities of color. Out of psychology and education have emerged a series of theories, tests, beliefs and practices that permeate every facet and level of the American education system, preschool to postsecondary and beyond. The work of early White psychological science pioneers such as Alfred Binet, Lewis Terman and Carl Brigham spawned an array of aptitude tests, achievement assessments and college entrance examinations that still dictate the educational and vocational options for millions worldwide.

Such tests often normed on the experiences, verbal and non-verbal language and culture of White people favor White, upper-income individuals while disadvantaging other demographic groups. Even with test revisions and updates, they continue to fall short in equitable and culturally responsive ways, as witnessed by limited educational access afforded to students of color and English Language Learners. It is no wonder that we and many scholars still call for more effective and inclusive systems of assessments.Dr. James L. Moore III

Let us be clear. The tests are not the sole issue. Instead, the issue is how people professionals use them in isolation of other critical information. The results are often taken too literally by educators, who use the tests to validate their expectations of minoritized groups. Reification is prevalent. They are used to hinder access togifted and talented programs, courses for advanced learners and access to higher education in general. Conversely, how tests are used plays a dominant role in the over-representation of Black students in stigmatized categories of special education. This is associated, along with excessive disciplining and hyper-policing of Black bodies in academic settings, with the school-to-prison pipeline.

The high-stakes decisions made by testing are carried by students for a lifetime. And so, the missteps outlined in the APA apology continue to reverberate through American schools, impacting our children, their potential and outcomes, as well as the achievement and progress of our entire nation. Therefore, the attitudes and perceptions about minoritized groups must be examined, and a systematic review should be undertaken of training and pedagogical approaches used in educational institutions.

The associations apology should have happened decades ago. The opportunity presented itself when the Civil Rights Act passed, during so many discussions of psychological health and well-being and, nearly two years ago, when George Floyd was murdered. Because of the outsized influence of psychology in other disciplines, organizations should self-examine and follow suit, including the National Association for Gifted Children, Council for Exceptional Children, National Association for the Education of Young Children, American Educational Research Association and the American Counseling Association, to name a few. All have observed their members impact on education and life outcomes using misguided science rooted in racist ideology. It is time to come clean, recognize our complex history and outline a path forward that is indicative of an authentic and sincere apology that leads to new possibilities.

Issuing statements does not fix the historical harm done. To make meaningful change, we must do the hard and messy work of examining the impact and finding commensurate solutions by going deep and wide. Lukewarm, band-aid solutions will not suffice. Gone is the time for allyship that only leads to more webinars with little outcome and accountability. The APA and education field can broadly begin here: Assess who uses psychological tests today, and how. Examine how life-changing decisions are made based on the results. Evaluate how their implementation allows some people to treat others unjustly.

We have the research tools and, hopefully now the will, to guide education, psychology and other disciplines toward equity and inclusive excellence. But the question remains: Will we take this crucial opportunity to do more than simply say, Were sorry? Now, more than ever, we must move along the arc of the moral universe.

Dr. Don Pope-Davis, is Dean of the College of Education and Human Ecology at The Ohio State University

Dr. James L. Moore III, is Vice Provost for Diversity and Inclusion and Chief Diversity Officer at The Ohio State University

Dr. Donna Y. Ford, is Distinguished Professor of Education and Human Ecology, at The Ohio State University

Read the original:

Time Will Tell: Three Black Scholars Ponder APA's Apology for Silence and Complicity in Perpetuating Racism - Diverse: Issues in Higher Education

Opinion: Dont be fooled. Zionism is an Indigenous rights movement and being anti-Zionist is antisemitic. – The San Diego Union-Tribune

Danzig served in the Israeli Army and is a former police officer with the New York Police Department. He is an attorney and active member of StandWithUs, where he is the local advisory board president, and Herut North American, where he is a national board member. He lives in Del Mar.

On Oct. 26, the San Diego Unified School District Board of Education passed a resolution condemning antisemitism, as its defined by the International Holocaust Remembrance Alliance (IHRA), and as requested by every synagogue and mainstream Jewish organization in San Diego. Since then, Israel-haters in San Diego have been wringing their virtual hands over the audacity of a school district to define antisemitism the way most Jews define it (in a state that over the previous five years saw a 40 percent increase in antisemitic hate crimes, and in a country where Jews are the targets of 60 percent of all faith-based hate crimes).

Recognizing they cant simply say that they oppose such resolutions because Israel-haters want to exploit Jew-hatred in order to incite hatred against Israel (the worlds only Jewish state and home to nearly half of the worlds Jews), the Israel-haters wax apoplectic about how the IHRA definition chills free speech because it supposedly makes legitimate criticism of Israel antisemitic, is a tool for weaponizing antisemitism, and will somehow increase anti-Arab or anti-Muslim hatred.

I addressed why these claims are specious and themselves antisemitic in an an essay last month.

Likely because the IHRA definition in pertinent part provides it is antisemitic to deny the Jewish people their right to self-determination, e.g., by claiming that the existence of a State of Israel is a racist endeavor, we are seeing claims that being anti-Zionist is not antisemitic, as well as claims by Israel-haters actually comparing Zionism with racist colonialist ideologies like Manifest Destiny (which was used to justify Americas westward expansion and brutal conquest of Native Americans).

These claims are false and also incredibly insulting to the vast majority of Jews, who either are Israeli or feel a very strong attachment to Israel. Moreover, these claims get to the core of why the Arab-Israeli conflict persists, and why, despite at least eight different peace and partition offers since 1937 (to create the first independent Arab state west of the Jordan River), no such offer has ever been accepted.

While the Israel-haters try to redefine Zionism to make it seem somehow equivalent to colonialist ideologies like Manifest Destiny, the truth is that the definition of Zionism is quite simple: Zionism is the belief that the Jewish people, like all other peoples, have a right to self-determination and sovereignty in part of their Indigenous homeland.

Not only is there nothing in the definition of Zionism that believes Jews are superior to any other people or race, the idea of Jews being Zionist and even willing to fight for their right to be sovereign in their homeland predates the phony European concept of race by over 1,500 years. We just finished celebrating Hanukkah. While many Americans may think Hanukkah is a Jewish version of Christmas, or just a fun, candle-lighting, jelly-donut-eating holiday, that would be incorrect. Not that Hanukkah isnt fun (it is), but at its core, Hanukkah is a celebration of a successful Jewish revolt in the land of Israel and the reestablishment, after centuries of Greek colonial rule, of Jewish sovereignty and self-determination in Zion (another word in Hebrew for Jerusalem).

Nearly 300 years after the successful Jewish revolt against the Greek/Selucid Empire, the Jewish peoples Zionism led to other Jewish revolts against colonial rule, this time against the Romans. From those ultimately unsuccessful revolts, archeologists have found numerous Judean coins, including coins inscribed in ancient Hebrew with the words: Freedom for Zion. It is that longing for freedom in Zion, the 3,000-plus year history of the land of Israels centrality in the Jewish peoples faith, culture and consciousness, coupled with the sad reality that the Jewish people have been regularly subjected to deadly discrimination and oppression in almost every land in the Diaspora, which led to the 19th century political movement called Zionism. And when Israel gained its independence in 1948, Zionism became the worlds first successful Indigenous movement of a dispossessed and colonized people regaining sovereignty in their Indigenous homeland.

Like many Indigenous peoples throughout the world, Jews were consistent victims of European oppression and violence for centuries, precisely because they were perceived as not being a part of the superior European world beginning with the Greek colonialization and attempted Hellenization of the land of Israel and continuing through World War II when over 6 million Jews were murdered. Throughout this time period, the Jewish peoples dream of freedom in Zion and for sovereignty in the land of Israel (what the Romans called Palestina) never waned. It is why at every Passover seder, and in countless other prayers, the Jewish people have regularly prayed and sang in Hebrew about their longing for a return to Zion.

It is this context that makes the arguments of the I am only anti-Zionist antisemites so clearly hollow. As Zionism simply stands for the proposition that the Jewish people have a right to sovereignty in part of their Indigenous and historical homeland, saying you are anti-Zionist, but not anti-Jewish, is the equivalent of saying you are not anti-Maori, but only want to deny the Maori any sovereignty in their Indigenous lands, or that you are not anti-Algonquin, Mississaugas, Odawa, Oji-Cree, Ojibwe, or Potawatomi, you just hate the Anishinaabe movement for a sovereign Native American state called Anishinaabaki.

As for those dishonestly comparing Zionism with Manifest Destiny, or other supremacist forms of colonialism, it bears noting that when the descendants of the English, French and Spanish conquered and colonized North America, they never discovered a single archeological finding written in ancient English, French or Spanish; but archeological artifacts written in Hebrew and referring to Jewish kings, Jewish prayers (that Jews still say to this day) and even to ancient vitners in the land of Israel are ubiquitous.

What the I am only anti-Zionist antisemites also ignore (or more aptly seek to deflect attention from) is how closely anti-Zionist tropes track antisemitic tropes, which for centuries were used to incite discrimination and violence against Jews.

The 19th-century antisemite demonized Jews, among all peoples on Earth, as the primary cause of the worlds problems. Anti-Zionists demonize Israel, the Jew among the nations, as the primary cause of the worlds problems. For the 19th-century antisemite, Jews were bloodthirsty baby killers. Anti-Zionists routinely demonize the one Jewish state as a bloodthirsty baby killer. The 19th-century antisemite demonized Jews as being nefariously in control of banks, the media and governments. Anti-Zionists regularly demonize Israel or Zionists as controlling the banks, media and foreign governments. The parallels are clear.

But the most antisemitic aspect of the anti-Zionist creed has to be the ubiquitous attempts to erase Jewish history and to tar Zionism as a colonialist endeavor. George Orwell famously said, The most effective way to destroy people is to deny and obliterate their own understanding of their history.

That erasure is at the core of anti-Zionism. It is also at the core of the Arab-Israeli conflict. Because ultimately, the anti-Zionists claims about colonialism are what psychologists refer to as projection. In the seventh and eighth centuries, Arab armies from the Arabian Peninsula conquered and colonized all of the Middle East and North Africa (MENA). Since then, their descendants, just like the descendants of Europeans in all of the lands conquered by Europeans, have generally resisted all Indigenous rights and independence movements. It is why over the past millennia, there has never been an independent state for the Kurds, Amazigh, Copts, or any other Indigenous people in the MENA (other than the Jewish people).

Antisemitism is the oldest form of bigotry. For over 2,000 years. it has led to countless expulsions and murders of Jews. Today, it includes anti-Zionism, a hatred of Jewish sovereignty and of the ability of Jews to defend themselves in their own state. Many want to paint this hatred as somehow being progressive, when the core motivation behind this hatred is a regressive desire to destroy the one successful Indigenous rights movement in the MENA, and to once again make Jews stateless and defenseless. No one should allow themselves to be taken in by such counterfactual duplicity.

See the original post here:

Opinion: Dont be fooled. Zionism is an Indigenous rights movement and being anti-Zionist is antisemitic. - The San Diego Union-Tribune