{"id":50195,"date":"2015-03-05T00:00:00","date_gmt":"2015-03-04T23:00:00","guid":{"rendered":"http:\/\/www.pcb.ub.edu\/rare-and-orphan-but-not-abandoned-by-science\/"},"modified":"2020-11-18T15:23:45","modified_gmt":"2020-11-18T14:23:45","slug":"rare-and-orphan-but-not-abandoned-by-science","status":"publish","type":"post","link":"https:\/\/www.pcb.ub.edu\/en\/rare-and-orphan-but-not-abandoned-by-science\/","title":{"rendered":"Rare and orphan but not abandoned by science"},"content":{"rendered":"<p>&#8220;Governments in<a href=\"http:\/\/www.eurordis.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">Europe<\/a>\u00a0and\u00a0<a href=\"http:\/\/www.ncats.nih.gov\/research\/rare-diseases\/rare-diseases.html\" target=\"_blank\" rel=\"noopener noreferrer\">US<\/a>\u00a0are encouraging the pharmaceutical industry to invest in rare diseases by accelerating, for example, the process of approving new drugs, and this stimulus has a positive rebound effect on basic research labs like ours. There is a lot of possible and achievable research that will favour the identification of therapeutic strategies for orphan diseases,&#8221; says Salvatella.<\/p>\n<p>His &#8220;Molecular Biophysics Lab&#8221; at IRB Barcelona started research into Kennedy&#8217;s disease with funding from the TV3 Telethon in 2010 and continues this line of investigation with resources from the National Research Plan of the Spanish Government. To date, the results are &#8220;quite positive and for 2020 we could have a drug tested in cells\u00a0in vitro,&#8221; he explains.<\/p>\n<p><strong>Kennedy&#8217;s disease<\/strong><\/p>\n<p>Muscular spinal bulbar atrophy or Kennedy&#8217;s disease is a rare degenerative hereditary condition that affects only men, approx. 1 in every 36.000, and has no treatment. Described in 1968 by the neurologist W. R. Kennedy, this disease causes the accumulation of aggregates of a protein called the androgen receptor, which are toxic for motor neurons and muscle cells.<\/p>\n<p>Although the origin and symptoms of this disease have been extensively described, there was a lack of knowledge about the nature of the toxic aggregates and how they form, thus impeding progress towards a drug. Salvatella&#8217;s lab is devoted to the study of protein folding and unfolding, and Kennedy&#8217;s disease is a pathology due to the misfolding of the androgen receptor. &#8220;There were no methods available to study the aggregation of this protein, nor the underlying biological problem at the molecular level. In five years, we have made significant progress in this issue, we know the mechanism of formation of the toxic aggregates and soon we will start work on designing new drugs,&#8221; explains the researcher, who adds that, &#8220;our case is an example of how a good environment can give rise to opportunities to rapidly further our understanding of rare diseases.&#8221;<\/p>\n<p>The conference on Friday will be the open the series &#8220;Barcelona BioMed Perspectives&#8221;, given by IRB Barcelona at CCCB, in the framework of IRB Barcelona&#8217;s 10th anniversary celebration (2005-2015).<\/p>\n<p>Under the title\u00a0<a href=\"http:\/\/www.irbbarcelona.org\/en\/events\/barcelona-biomed\/barcelona-biomed-perspectives\" target=\"_blank\" rel=\"noopener noreferrer\">&#8220;Science today for the medicine of the future&#8221;<\/a>, IRB is offering public talks to raise awareness of the advances and challenges faced by researchers with respect to the medicine of the future. The conference series includes sessions on Cancer and metastasis (27 May), Alzheimer&#8217;s disease (17 September) and Diabetes (5 November).<\/p>\n","protected":false},"excerpt":{"rendered":"<p>On Friday 6 March at 19h in &#8220;Centre de Cultura Contempor\u00e0nia de Barcelona&#8221; (CCCB),\u00a0Xavier Salvatella, ICREA researcher at the Institute for Research in Biomedicine (<a href=\"http:\/\/www.irbbarcelona.org\/en\" target=\"_blank\" rel=\"noopener noreferrer\">IRB Barcelona<\/a>) \u2013based in the PCB\u2013 will give a public conference (free of charge) on rare diseases. In a presentation entitled\u00a0<a href=\"http:\/\/www.cccb.org\/en\/curs_o_conferencia-rare_diseases-212728\" target=\"_blank\" rel=\"noopener noreferrer\">&#8220;Kennedy&#8217;s disease, an example of new scientific research approaches to understand rare diseases&#8221;,<\/a>\u00a0Salvatella will explain the changing scenario of rare diseases, exemplified by studies on Kennedy&#8217;s disease performed in his basic research lab\u2014a line of investigation launched in 2010.<\/p>\n","protected":false},"author":1,"featured_media":55700,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"inline_featured_image":false,"footnotes":""},"categories":[8],"tags":[],"class_list":["post-50195","post","type-post","status-publish","format-standard","has-post-thumbnail","category-uncategorized"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Rare and orphan but not abandoned by science - Parc Cient\u00edfic de Barcelona<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.pcb.ub.edu\/en\/rare-and-orphan-but-not-abandoned-by-science\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Rare and orphan but not abandoned by science - Parc Cient\u00edfic de Barcelona\" \/>\n<meta property=\"og:description\" content=\"On Friday 6 March at 19h in &quot;Centre de Cultura Contempor\u00e0nia de Barcelona&quot; (CCCB),\u00a0Xavier Salvatella, ICREA researcher at the Institute for Research in Biomedicine (IRB Barcelona) \u2013based in the PCB\u2013 will give a public conference (free of charge) on rare diseases. 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