{"id":27886,"date":"2014-03-25T07:42:33","date_gmt":"2014-03-25T11:42:33","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/triple-negative-breast-cancers-progression-and-relapse-pinned-to-a-gene\/"},"modified":"2014-03-25T07:42:33","modified_gmt":"2014-03-25T11:42:33","slug":"triple-negative-breast-cancers-progression-and-relapse-pinned-to-a-gene","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/gene-medicine\/triple-negative-breast-cancers-progression-and-relapse-pinned-to-a-gene\/","title":{"rendered":"Triple Negative Breast Cancer&#39;s Progression and Relapse Pinned to a Gene"},"content":{"rendered":"<p><p>Contact Information         <\/p>\n<p>      Available for logged-in reporters only    <\/p>\n<p>    Newswise  HOUSTON -- (March 24, 2014) -- Scientists from    Houston Methodist and Weill Cornell Medical College have found    that a gene previously unassociated with breast cancer plays a    pivotal role in the growth and progression of the triple    negative form of the disease, which can be particularly deadly,    with few treatment options. Their research, published in the    April 3 Nature (online today), suggests that targeting    the gene may be a new approach to treat the disease.  <\/p>\n<p>    \"We are really beginning to understand what initiates the    cancer and why cancer cells evade treatment,\" said coauthor and    Houston Methodist Cancer Center Director Jenny Chang, M.D. \"Our    group learned this pathway was activated in about two-thirds of    patients with this type of breast cancer, and we believe we may    be able to treat the disease by manipulating elements of the    pathway.\"  <\/p>\n<p>    About 42,000 new cases of triple negative breast cancer (TNBC)    are diagnosed in the United States each year, about 20 percent    of all breast cancer diagnoses. Patients who relapse typically    do so within one to three years of being treated.  <\/p>\n<p>    Senior author Laurie H. Glimcher, M.D., the Stephen and Suzanne    Weiss Dean of Weill Cornell Medical College, wanted to know    whether the gene -- already understood from her prior work to    be a critical regulator of immune and metabolic functions --    was important to cancer's ability to adapt and thrive in the    oxygen- and nutrient-deprived environments inside of tumors.    Using cells taken from patients' tumors and transplanted into    mice, Glimcher's team found that the gene, XBP1, is    especially active in TNBC, particularly in the progression of    malignant cells and their resurgence after treatment.  <\/p>\n<p>    \"Patients with the triple negative form of breast cancer are    those who most desperately need new approaches to treat their    disease,\" said Glimcher, who is also a professor of medicine at    Weill Cornell. \"This pathway was activated in about two-thirds    of patients with this type of breast cancer. Now that we better    understand how this gene helps tumors proliferate and then    return after a patient's initial treatment, we believe we can    develop more effective therapies to shrink their growth and    delay relapse.\"  <\/p>\n<p>    The group, which included investigators from nine institutions,    examined several types of breast cancer cell lines. They found    that XBP1 was particularly active in basal-like breast cancer    cells cultivated in the lab and in TNBC cells from patients.    When they suppressed the activity of the gene in laboratory    cell cultures and animal models, however, the researchers were    able to dramatically reduce the size of tumors and the    likelihood of relapse, especially when these approaches were    used in conjunction with the chemotherapy drugs doxorubicin or    paclitaxel. The finding suggests that XBP1 controls behaviors    associated with tumor-initiating cells that have been    implicated as the originators of tumors in a number of cancers,    including that of the breast, supporting the hypothesis that    combination therapy could be an effective treatment for TNBC.  <\/p>\n<p>    The scientists also found that interactions between XBP1 and    another transcriptional regulator, HIF1-alpha, spurs the    cancer-driving proteins. Silencing XBP1 in the TNBC cell    lines reduced the tumor cells' growth and other behaviors    typical of metastasis.  <\/p>\n<p>    \"This starts to demonstrate how cancer cells co-opt the    endoplasmic reticulum stress response pathway to allow tumors    to grow and survive when they are deprived of nutrients and    oxygen,\" said lead author Xi Chen, Ph.D., a postdoctoral    associate at Weill Cornell, referring to the process by which    healthy cells maintain their function. \"It shows the    interaction between two critical pathways to make the cells    better able to deal with a hostile microenvironment, and in    that way offers new strategies to target triple negative breast    cancer.\"  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Read more:<br \/>\n<a target=\"_blank\" href=\"http:\/\/www.newswise.com\/articles\/view\/615492\/?sc=rsmn\/RS=^ADA_FgIyDG89rdHem3JKIk71CbN25E-\" title=\"Triple Negative Breast Cancer&#39;s Progression and Relapse Pinned to a Gene\">Triple Negative Breast Cancer&#39;s Progression and Relapse Pinned to a Gene<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Contact Information Available for logged-in reporters only Newswise HOUSTON -- (March 24, 2014) -- Scientists from Houston Methodist and Weill Cornell Medical College have found that a gene previously unassociated with breast cancer plays a pivotal role in the growth and progression of the triple negative form of the disease, which can be particularly deadly, with few treatment options. Their research, published in the April 3 Nature (online today), suggests that targeting the gene may be a new approach to treat the disease.  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/gene-medicine\/triple-negative-breast-cancers-progression-and-relapse-pinned-to-a-gene\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[21],"tags":[],"class_list":["post-27886","post","type-post","status-publish","format-standard","hentry","category-gene-medicine"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/27886"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=27886"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/27886\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=27886"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=27886"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=27886"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}