Identification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic muscles

One potential approach for the treatment of Duchenne muscular dysrophy is to increase expression of the dystrophin homolog utrophin. Here, the authors show that eEF1A2 regulates utrophin expression, and show that 2 FDA-approved drugs upregulate eEIF1A2 and utrophin level in mice, leading to improvem...

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Autores principales: Christine Péladeau, Nadine Adam, Lucas M. Bronicki, Adèle Coriati, Mohamed Thabet, Hasanen Al-Rewashdy, Jason Vanstone, Alan Mears, Jean-Marc Renaud, Martin Holcik, Bernard J. Jasmin
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Lenguaje:EN
Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/6bc7a05ce66e4135bb35be45df6c5df1
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spelling oai:doaj.org-article:6bc7a05ce66e4135bb35be45df6c5df12021-12-02T14:40:29ZIdentification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic muscles10.1038/s41467-020-15971-w2041-1723https://doaj.org/article/6bc7a05ce66e4135bb35be45df6c5df12020-04-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-15971-whttps://doaj.org/toc/2041-1723One potential approach for the treatment of Duchenne muscular dysrophy is to increase expression of the dystrophin homolog utrophin. Here, the authors show that eEF1A2 regulates utrophin expression, and show that 2 FDA-approved drugs upregulate eEIF1A2 and utrophin level in mice, leading to improvement of the dystrophic phenotype.Christine PéladeauNadine AdamLucas M. BronickiAdèle CoriatiMohamed ThabetHasanen Al-RewashdyJason VanstoneAlan MearsJean-Marc RenaudMartin HolcikBernard J. JasminNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Christine Péladeau
Nadine Adam
Lucas M. Bronicki
Adèle Coriati
Mohamed Thabet
Hasanen Al-Rewashdy
Jason Vanstone
Alan Mears
Jean-Marc Renaud
Martin Holcik
Bernard J. Jasmin
Identification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic muscles
description One potential approach for the treatment of Duchenne muscular dysrophy is to increase expression of the dystrophin homolog utrophin. Here, the authors show that eEF1A2 regulates utrophin expression, and show that 2 FDA-approved drugs upregulate eEIF1A2 and utrophin level in mice, leading to improvement of the dystrophic phenotype.
format article
author Christine Péladeau
Nadine Adam
Lucas M. Bronicki
Adèle Coriati
Mohamed Thabet
Hasanen Al-Rewashdy
Jason Vanstone
Alan Mears
Jean-Marc Renaud
Martin Holcik
Bernard J. Jasmin
author_facet Christine Péladeau
Nadine Adam
Lucas M. Bronicki
Adèle Coriati
Mohamed Thabet
Hasanen Al-Rewashdy
Jason Vanstone
Alan Mears
Jean-Marc Renaud
Martin Holcik
Bernard J. Jasmin
author_sort Christine Péladeau
title Identification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic muscles
title_short Identification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic muscles
title_full Identification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic muscles
title_fullStr Identification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic muscles
title_full_unstemmed Identification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic muscles
title_sort identification of therapeutics that target eef1a2 and upregulate utrophin a translation in dystrophic muscles
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/6bc7a05ce66e4135bb35be45df6c5df1
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