{"id":213,"date":"2011-11-10T12:37:05","date_gmt":"2011-11-10T12:37:05","guid":{"rendered":"https:\/\/blogs.nature.com\/spoonful\/2011\/11\/news-feature-a-raw-nerve.html"},"modified":"2011-11-10T12:37:05","modified_gmt":"2011-11-10T12:37:05","slug":"news_feature_a_raw_nerve","status":"publish","type":"post","link":"https:\/\/blogs.nature.com\/spoonful\/2011\/11\/news_feature_a_raw_nerve.html","title":{"rendered":"NEWS FEATURE: A raw nerve"},"content":{"rendered":"<p><em>By Virginia Hughes<\/em><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" alt=\"nm1111-1333-I1.jpg\" src=\"https:\/\/blogs.nature.com\/spoonful\/files\/nm1111-1333-I1.jpg\" width=\"200\" height=\"133\" align=\"right\" hspace=\"10px\"\/>At a walkathon one Saturday in September, nearly 5,000 people traced two miles of Chicago&#8217;s lakefront to raise money for research into the progressive nerve disease that is thought to have killed baseball star Lou Gehrig. <a href=\"https:\/\/neurogenetics.northwestern.edu\/rteam.html\">Janice Caliendo<\/a> was there collecting blood samples from friends of those affected by the incurable disease to be used as controls in future genetic studies. Caliendo, a lab manager at Northwestern Memorial Hospital in the Streeterville neighborhood of the city, often attends these sorts of fundraisers, but this time she was getting more attention than usual.<\/p>\n<p>Her lab, headed by Northwestern University neurologist <a href=\"https:\/\/www.neurology.northwestern.edu\/faculty\/siddique.html\">Teepu Siddique<\/a>, has been all over the news recently for a <a href=\"https:\/\/www.nature.com\/nature\/journal\/v477\/n7363\/full\/nature10353.html\">study<\/a> published in August in <em>Nature<\/em> reporting a new gene associated with the disease formally known as amyotrophic lateral sclerosis (<span class=\"caps\">ALS<\/span>). \u201cBreakthrough could lead to effective treatment for Lou Gehrig&#8217;s disease,\u201d read the <em>LA Times<\/em>&#8216;s <a href=\"https:\/\/mobile.latimes.com\/p.p?a=rp&#038;m=b&#038;postId=734288&#038;curAbsIndex=2&#038;resultsUrl=DID%3D1%26DFCL%3D1000%26DSB%3Drank%2523desc%26DBFQ%3DuserId%253A7%26DL.w%3D%26DL.d%3D10%26DQ%3DsectionId%253A6890%26DPS%3D0%26DPL%3D3\">headline<\/a>; \u201cCause of <span class=\"caps\">ALS<\/span> is found, Northwestern team says,\u201d <a href=\"https:\/\/articles.chicagotribune.com\/2011-08-22\/news\/ct-met-northwestern-als-breakthrough-20110822_1_als-patients-siddique-key-protein\">wrote<\/a> the <em>Chicago Tribune<\/em>. In honor of the study, in fact, the event&#8217;s organizers asked Siddique to lead the walkathon. Countless people approached Caliendo that day with the same questions: Does this mean there&#8217;s a cure? Is there a blood test for <span class=\"caps\">ALS<\/span>? Is there a drug to treat it?<\/p>\n<p>The answer to all these inquiries was &#8216;no&#8217;. \u201cIt&#8217;s not a cure, but people read into it what they want to hear,\u201d Caliendo says. \u201cI don&#8217;t think they were disappointed, though, because it&#8217;s still very good news. It&#8217;s huge.\u201d<\/p>\n<p>The study, some two decades in the making, was certainly newsworthy: it uncovered mutations in a gene called <em>UBQLN2<\/em> that seemed to cause <span class=\"caps\">ALS<\/span> in a handful of individuals with hereditary forms of the disease. But, according to Siddique, that&#8217;s not even the exciting part. In the new paper, his team analyzed postmortem spinal cord tissue from dozens of people with different forms of the disease, including those who developed <span class=\"caps\">ALS<\/span> spontaneously and didn&#8217;t carry <em>UBQLN2<\/em> mutations. To their surprise, Siddique and his colleagues found abnormal blobs of the ubiquilin-2 protein encoded by <em>UBQLN2<\/em> in the neurons of every single individual they looked at.<\/p>\n<p>In Siddique&#8217;s view, his study proves that all forms of <span class=\"caps\">ALS<\/span> converge on a glitch in protein recycling that results in the accumulation of many types of proteins and the death of motor neurons. It&#8217;s similar, he says, to the discovery decades ago that people with a genetic disease called familial hypercholesterolemia carry mutations in a receptor for &#8216;bad&#8217; cholesterol. On the basis of those data, researchers designed drugs\u2014statins\u2014that are now taken not only by those affected by the rare disorder but also by the majority of people with all forms of heart disease in the developed world.<\/p>\n<p>\u201cWhat we&#8217;re showing here is a direct functional mechanism that causes disease,\u201d Siddique says. \u201cIt&#8217;s not just another cause; it&#8217;s not just another pathology; it&#8217;s a game changer.\u201d<\/p>\n<p><em>(Click <a href=\"https:\/\/www.nature.com\/nm\/journal\/v17\/n11\/full\/nm1111-1333.html\">here<\/a> to continue reading.)<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>By Virginia Hughes At a walkathon one Saturday in September, nearly 5,000 people traced two miles of Chicago&#8217;s lakefront to raise money for research into the progressive nerve disease that is thought to have killed baseball star Lou Gehrig. Janice Caliendo was there collecting blood samples from friends of those affected by the incurable disease to be used as controls in future genetic studies. Caliendo, a lab manager at Northwestern Memorial Hospital in the Streeterville neighborhood of the city, often attends these sorts of fundraisers, but this time she was getting more attention than usual. Her lab, headed by Northwestern&nbsp; <a href=\"https:\/\/blogs.nature.com\/spoonful\/2011\/11\/news_feature_a_raw_nerve.html#wpn-more-213\" class=\"more-link\"> &hellip; Read more<\/a> <a href=\"https:\/\/blogs.nature.com\/spoonful\/2011\/11\/news_feature_a_raw_nerve.html\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":128,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[10,3],"tags":[],"class_list":["post-213","post","type-post","status-publish","format-standard","hentry","category-neurosciencemental-health","category-print"],"_links":{"self":[{"href":"https:\/\/blogs.nature.com\/spoonful\/wp-json\/wp\/v2\/posts\/213","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blogs.nature.com\/spoonful\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/blogs.nature.com\/spoonful\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.nature.com\/spoonful\/wp-json\/wp\/v2\/users\/128"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.nature.com\/spoonful\/wp-json\/wp\/v2\/comments?post=213"}],"version-history":[{"count":0,"href":"https:\/\/blogs.nature.com\/spoonful\/wp-json\/wp\/v2\/posts\/213\/revisions"}],"wp:attachment":[{"href":"https:\/\/blogs.nature.com\/spoonful\/wp-json\/wp\/v2\/media?parent=213"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.nature.com\/spoonful\/wp-json\/wp\/v2\/categories?post=213"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.nature.com\/spoonful\/wp-json\/wp\/v2\/tags?post=213"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}