Chemotherapeutic agent 5-fluorouracil increases survival of SOD1 mouse model of ALS

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...

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Veröffentlicht in:PloS one 2019-01, Vol.14 (1), p.e0210752-e0210752
Hauptverfasser: Rando, Amaya, de la Torre, Miriam, Martinez-Muriana, Anna, Zaragoza, Pilar, Musaro, Antonio, Hernández, Sara, Navarro, Xavier, Toivonen, Janne M, Osta, Rosario
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Sprache:eng
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Zusammenfassung: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.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0210752