{"id":189893,"date":"2015-03-09T10:52:35","date_gmt":"2015-03-09T14:52:35","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/a-new-opportunity-to-treat-drug-resistant-leukemia-discovered.php"},"modified":"2015-03-09T10:52:35","modified_gmt":"2015-03-09T14:52:35","slug":"a-new-opportunity-to-treat-drug-resistant-leukemia-discovered","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/molecular-medicine\/a-new-opportunity-to-treat-drug-resistant-leukemia-discovered.php","title":{"rendered":"A new opportunity to treat drug-resistant leukemia discovered"},"content":{"rendered":"<p><p>  A public-private research collaboration leads to an unexpected  discovery in patients with drug-resistant leukemia<\/p>\n<p>    Helsinki - February 9, 2015 - A study led by researchers at the    Institute for Molecular Medicine Finland FIMM and Faculty of    Medicine, University of Helsinki and the Helsinki University    Central Hospital Comprehensive Cancer Center, in close    collaboration with researchers at Pfizer, has identified a    previously unrecognized action of Pfizer's axitinib as a potent    inhibitor of the dominant mutation that confers drug resistance    to all well tolerated treatments in patients with certain types    of leukemia. The findings of this international joint effort    were published online today, 9 February, 2015, in the journal    Nature.  <\/p>\n<p>    The FIMM research team studied cancer cells from patients with    chronic myelogenous and acute lymphoblastic leukemia (CML and    ALL) that had developed resistance to currently available    treatments. These cancers are driven by the BCR-ABL1 fusion    protein, and resistance to treatment developed due to a new    genetic mutation in the BCR-ABL1 fusion gene in the cancer    cells.  <\/p>\n<p>    There were two critical factors that were integral to the    outcome of this study. First, the Drug Sensitivity and    Resistance Testing (DSRT) method developed at FIMM made it    possible to study the response of these cancer patients'    leukemia cells to a large panel of drugs simultaneously, thus    identifying axitinib as a promising drug candidate. Using this    approach, the researchers found that axitinib, a tyrosine    kinase inhibitor currently approved to treat certain patients    with advanced renal cell carcinoma, effectively eliminated    these patient-derived drug resistant leukemia cells.  <\/p>\n<p>    \"This screening method is a key component of FIMM's    Individualized Systems Medicine strategy. The drug panel covers    all approved and many emerging cancer therapeutics, and thus    enables an individualized selection of potentially effective    therapies for leukemia patients,\" explains Krister Wennerberg,    FIMM-EMBL Group Leader and a corresponding study author.  <\/p>\n<p>    Second, by coupling this screening method with Pfizer's deep    oncology and structure-based drug discovery expertise, the    researchers were also able to define the mechanism by which    axitinib binds to the drug resistant version of the BCR-ABL1    protein, providing fundamental new molecular insights into how    cancer causing kinases can be blocked.  <\/p>\n<p>    \"If you think of the targeted protein as a lock into which the    cancer drug fits in as a key, the resistant protein changes in    such a way that we need a different key. In the case of    axitinib, it acts as two distinct keys - one for renal cell    carcinoma and one for leukemia\" says Brion Murray, Pfizer    Research Fellow and one of the lead authors of the study.  <\/p>\n<p>    \"Since axitinib is already used to treat cancer, its safety is    known and a formal exploration of its clinical utility in drug    resistant leukemia can now be done in a fast-track mode. Thus,    the normally very long path from lab bench to bedside is now    significantly shortened,\" says Kimmo Porkka, Head of Hematology    at Helsinki University Central Hospital Comprehensive Cancer    Center and one of the lead authors.  <\/p>\n<p>    \"Our findings highlight the power of drug repositioning, in    other words, searching for novel uses for existing, emerging    and abandoned drugs. This study shows what can be achieved when    academic institutions and pharmaceutical companies team up to    study effects of drugs using cells directly obtained from    patients,\" says Olli Kallioniemi, the Director of FIMM.  <\/p>\n<p>    \"This high caliber publication is a great example of Pfizer's    strong collaboration with academia to further advance research    for patients with cancer,\" adds Murray. \"Further research will    determine whether these findings have the potential to    significantly improve the standard of care for this select    group of CML patients and patients with other related    leukemias.\"  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Here is the original post:<\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.eurekalert.org\/pub_releases\/2015-02\/uoh-ano020915.php\/RK=0\/RS=2MzNj_SZYC3Vwqg_bf2hqzIphZ8-\" title=\"A new opportunity to treat drug-resistant leukemia discovered\">A new opportunity to treat drug-resistant leukemia discovered<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> A public-private research collaboration leads to an unexpected discovery in patients with drug-resistant leukemia Helsinki - February 9, 2015 - A study led by researchers at the Institute for Molecular Medicine Finland FIMM and Faculty of Medicine, University of Helsinki and the Helsinki University Central Hospital Comprehensive Cancer Center, in close collaboration with researchers at Pfizer, has identified a previously unrecognized action of Pfizer's axitinib as a potent inhibitor of the dominant mutation that confers drug resistance to all well tolerated treatments in patients with certain types of leukemia.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/molecular-medicine\/a-new-opportunity-to-treat-drug-resistant-leukemia-discovered.php\">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":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[26],"tags":[],"class_list":["post-189893","post","type-post","status-publish","format-standard","hentry","category-molecular-medicine"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/189893"}],"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\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=189893"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/189893\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=189893"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=189893"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=189893"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}