{"id":45015,"date":"2012-05-17T12:22:39","date_gmt":"2012-05-17T12:22:39","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/finnish-researchers-identified-the-cause-for-lgl-leukemia.php"},"modified":"2012-05-17T12:22:39","modified_gmt":"2012-05-17T12:22:39","slug":"finnish-researchers-identified-the-cause-for-lgl-leukemia","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/molecular-medicine\/finnish-researchers-identified-the-cause-for-lgl-leukemia.php","title":{"rendered":"Finnish researchers identified the cause for LGL leukemia"},"content":{"rendered":"<p><p>Public  release date: 16-May-2012  [ |   E-mail   |  Share    ]  <\/p>\n<p>    Contact: Dr. Satu Mustjoki    <a href=\"mailto:satu.mustjoki@helsinki.fi\">satu.mustjoki@helsinki.fi<\/a>    358-947-171-898    University of Helsinki<\/p>\n<p>    LGL leukemia is a relatively rare, malignant blood disease of    the mature T-cells and, in many cases, it is related to    autoimmune diseases such as rheumatoid arthritis. The    pathogenetic mechanism of the disease has been unknown and it    has previously been unclear if the disease is an overreaction    of the normal defense system or a malignant hematological    disease.  <\/p>\n<p>    One of the key symptoms of LGL disease is a low count of white    blood cells (neutrophils), which may predispose the patients to    life-threatening infections.  <\/p>\n<p>    It was discovered that patients suffering from LGL leukemia    have a mutation in the STAT3 gene in a very restricted SH2    area, which has a key effect on the function of the gene. This    is not an inherited gene mutation but a so-called acquired    mutation. The cause for the mutation is not known, but probably    chronic viral infection or some other long-term antigen    exposure can be predisposing factors. The STAT3 gene plays a    key role in many cell signaling pathways.  <\/p>\n<p>    After the finding, the prevalence of the mutation in LGL    patients was verified using a larger patient group (77    patients) in cooperation with research groups at the Ohio    (Prof. Maciejewski) and Pennsylvania (Prof. Loughran)    Universities. It was discovered that 40% of all LGL patients    present with the STAT3 mutation.  <\/p>\n<p>    In the future, this result can be utilized in diagnosing the    disease and possibly also in treatment, since the first STAT3    inhibitors are already undergoing early clinical trials. In    addition, the research discovered that those LGL patients who    had a mutation in the STAT3 gene were also more likely to    suffer from rheumatoid arthritis. Hence, the research group    intends to clarify next if patients suffering from rheumatoid    arthritis can be found with similar gene mutations. If such    mutations were to be found this would introduce new    opportunities to the pathogenetic mechanisms of rheumatoid    arthritis and other autoimmune diseases.  <\/p>\n<p>    ###  <\/p>\n<\/p>\n<p>        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.  <\/p>\n<\/p>\n<p>Read more from the original source:<\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.eurekalert.org\/pub_releases\/2012-05\/uoh-fri051512.php\" title=\"Finnish researchers identified the cause for LGL leukemia\">Finnish researchers identified the cause for LGL leukemia<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Public release date: 16-May-2012 [ | E-mail | Share ] Contact: Dr.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/molecular-medicine\/finnish-researchers-identified-the-cause-for-lgl-leukemia.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-45015","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\/45015"}],"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=45015"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/45015\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=45015"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=45015"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=45015"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}