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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1371/journal.pone.0210752</dc:identifier><dc:language>eng</dc:language><dc:creator>Rando, A.</dc:creator><dc:creator>de la Torre, M.</dc:creator><dc:creator>Martinez-Muriana, A.</dc:creator><dc:creator>Zaragoza, P.</dc:creator><dc:creator>Musaro, A.</dc:creator><dc:creator>Hernández, S.</dc:creator><dc:creator>Navarro, X.</dc:creator><dc:creator>Toivonen, J.M.</dc:creator><dc:creator>Osta, R.</dc:creator><dc:title>Chemotherapeutic agent 5-fluorouracil increases survival of SOD1 mouse model of ALS</dc:title><dc:identifier>ART-2019-109675</dc:identifier><dc:description>Amyotrophic lateral sclerosis (ALS) is a lethal motor neuron disease with no cure. Currently there are only two ALS drugs approved by the FDA, both with a limited therapeutic effect. In the search for drug candidates for ALS, we studied the effect of known stem cell mobilizing agents (treatment) and antimetabolite 5-fluorouracil (5-FU) (anti-treatment) in SOD1G93A model of ALS. Surprisingly, we found that anti-cancer drug 5-FU increases lifespan, delays the disease onset and improves motor performance in ALS mice. Although we were not able to demonstrate the mechanistic basis of the beneficial 5-FU action in ALS mice, our findings suggest that 5-FU or similar drugs are possible drug candidates for the treatment of motor neuron diseases through drug repurposing.</dc:description><dc:date>2019</dc:date><dc:source>http://zaguan.unizar.es/record/76990</dc:source><dc:doi>10.1371/journal.pone.0210752</dc:doi><dc:identifier>http://zaguan.unizar.es/record/76990</dc:identifier><dc:identifier>oai:zaguan.unizar.es:76990</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/FIS/PI14-00947</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/FIS/PI17-00949</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/CB06-05-1105</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/RD12-0019-0011</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/RD16-0011-0035</dc:relation><dc:identifier.citation>PLoS ONE 14, 1 (2019), e0210752 [16pp]</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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