{"id":254272,"date":"2012-07-05T01:13:20","date_gmt":"2012-07-05T01:13:20","guid":{"rendered":"http:\/\/www.eugenesis.com\/cancer-therapeutics-reveals-proof-of-concept-for-second-development-drug\/"},"modified":"2012-07-05T01:13:20","modified_gmt":"2012-07-05T01:13:20","slug":"cancer-therapeutics-reveals-proof-of-concept-for-second-development-drug","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/biology\/cancer-therapeutics-reveals-proof-of-concept-for-second-development-drug.php","title":{"rendered":"Cancer Therapeutics Reveals Proof of Concept for Second Development Drug"},"content":{"rendered":"<p><p>    MELBOURNE, Australia--(BUSINESS WIRE)--  <\/p>\n<p>    Cancer Therapeutics, a company focused on translating cancer    biology research into novel treatments for cancer, today    announced the validation and performance of a new targeted    drug, CTx-294886, in combination with Avastin (bevacizumab     Genentech\/Roche) in a preclinical model of breast cancer. At    the same time the Company announced that it has developed a new    High Throughput Screening (HTS) platform for the identification    of small molecule inhibitors of protein ubiquitination, a key    element in the essential cellular process of protein    homeostasis, which is an exciting new target pathway for cancer    treatment. Both scientific developments will be presented as    posters at the EACR conference in Barcelona Spain on July 7-10    2012.  <\/p>\n<p>    The anti-tumour response to CTx-0294886, a potent small    molecule inhibitor of Focal Adhesion Kinase (FAK) and Vascular    Endothelial Growth Factor Receptor 3 (VEGFR3), was compared    with that of the Companys first product CTx-0294945, a potent    selective FAK inhibitor. CTx-0294886 in combination with    Avastin, showed additional benefits to those    previously demonstrated by CTx-294945 (previously presented at    the AACR conference in Chicago on the 3rd of April    this year). In both cases the small molecules in combination    with Avastin inhibited angiogenesis, and increased the    duration of tumour response in a model of basal breast cancer.    In addition CTx-294886 in combination with Avastin also    provided a highly statistically significant increase in the    median survival time compared to the Avastin only group.  <\/p>\n<p>    The new Ubiquitin HTS platform closely replicates cellular    ubiquitination pathways, and provides a mechanism for HTS of    multiple targets. Ubiquitins are small regulatory proteins that    attach to other target proteins allowing their destruction and    recycling. This process requires a family of dedicated enzymes,    such as ligases, for completion. E6AP, an E3 ligase, was    selected to validate the platform. E6AP ubiquitinates p53 and    PML in human papilloma virus (HPV) related and other cancers.    Both p53 and PML are well known suppressors of tumour growth so    substances that inhibit E6AP would be expected to retard tumour    growth in cancers such as cervical and head and neck cancers.    The platform was able to identify several small molecules that    are now undergoing further investigation.  <\/p>\n<p>    Dr Warwick Tong, CEO of Cancer Therapeutics, commented:  <\/p>\n<p>    Having achieved preclinical validation for our first product    candidate in conjunction with Avastin, we are delighted to be    announcing that our second candidate is even more potent at    prolonging and strengthening the effects of Avastin. We are    excited to have two targeted molecules that will allow rational    combinations with other therapies in the fight against cancer.    We are now starting to reap the benefits of our highly    collaborative approach to drug discovery, working hand in hand    with some of the top research institutes in Australia and our    international partner, Cancer Research Technology UK.  <\/p>\n<p>    Dr Ian Street, Chief Scientific Officer of Cancer Therapeutics,    added:  <\/p>\n<p>    The launch of our new Ubiquitin HTS platform opens up the    potential to collaborate with industry by screening chemical    libraries to address multiple targets in this new and exciting    area of cancer biology. We are ready to begin discussions with    other companies who would like to work with us to include their    targets of interest and screen their chemical libraries using    this platform.  <\/p>\n<p>    The titles of the posters being presented throughout the    conference are:  <\/p>\n<p>    Poster 846: Inhibition of Focal Adhesion Kinase in Combination    With Bevacizumab Reduces the Rate of Tumour Revascularization    and Increases Survival in a Pre-clinical Model of Basal Breast    Cancer by I. Street et al.  <\/p>\n<\/p>\n<p>More:<br \/>\n<a target=\"_blank\" href=\"http:\/\/finance.yahoo.com\/news\/cancer-therapeutics-reveals-proof-concept-230000570.html;_ylt=A2KJjakp6vRPgTYAgov_wgt.\" title=\"Cancer Therapeutics Reveals Proof of Concept for Second Development Drug\">Cancer Therapeutics Reveals Proof of Concept for Second Development Drug<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> MELBOURNE, Australia--(BUSINESS WIRE)-- Cancer Therapeutics, a company focused on translating cancer biology research into novel treatments for cancer, today announced the validation and performance of a new targeted drug, CTx-294886, in combination with Avastin (bevacizumab Genentech\/Roche) in a preclinical model of breast cancer. At the same time the Company announced that it has developed a new High Throughput Screening (HTS) platform for the identification of small molecule inhibitors of protein ubiquitination, a key element in the essential cellular process of protein homeostasis, which is an exciting new target pathway for cancer treatment.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/biology\/cancer-therapeutics-reveals-proof-of-concept-for-second-development-drug.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":57,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[577690],"tags":[],"class_list":["post-254272","post","type-post","status-publish","format-standard","hentry","category-biology"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/254272"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/57"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=254272"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/254272\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=254272"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=254272"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=254272"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}