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    <subfield code="a">Rando, A.</subfield>
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    <subfield code="a">Chemotherapeutic agent 5-fluorouracil increases survival of SOD1 mouse model of ALS</subfield>
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    <subfield code="a">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.</subfield>
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    <subfield code="a">de la Torre, M.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-7955-7164</subfield>
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    <subfield code="a">Martinez-Muriana, A.</subfield>
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    <subfield code="a">Zaragoza, P.</subfield>
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    <subfield code="a">Toivonen, J.M.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-7243-1737</subfield>
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    <subfield code="a">Osta, R.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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    <subfield code="b">Dpto. Anatom.,Embri.Genét.Ani.</subfield>
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    <subfield code="g">14, 1 (2019), e0210752 [16pp]</subfield>
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