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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Main Authors: 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
Format: Article
Language:English
Published: Nature Portfolio 2020-04-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-020-15971-w
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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
collection DOAJ
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.
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spelling doaj.art-6bc7a05ce66e4135bb35be45df6c5df12022-12-21T22:54:44ZengNature PortfolioNature Communications2041-17232020-04-0111111410.1038/s41467-020-15971-wIdentification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic musclesChristine Péladeau0Nadine Adam1Lucas M. Bronicki2Adèle Coriati3Mohamed Thabet4Hasanen Al-Rewashdy5Jason Vanstone6Alan Mears7Jean-Marc Renaud8Martin Holcik9Bernard J. Jasmin10Department of Cellular and Molecular Medicine, Faculty of Medicine, University of OttawaDepartment of Cellular and Molecular Medicine, Faculty of Medicine, University of OttawaDepartment of Cellular and Molecular Medicine, Faculty of Medicine, University of OttawaDepartment of Cellular and Molecular Medicine, Faculty of Medicine, University of OttawaDepartment of Cellular and Molecular Medicine, Faculty of Medicine, University of OttawaDepartment of Cellular and Molecular Medicine, Faculty of Medicine, University of OttawaApoptosis Research Centre, Children’s Hospital of Eastern Ontario Research InstituteApoptosis Research Centre, Children’s Hospital of Eastern Ontario Research InstituteDepartment of Cellular and Molecular Medicine, Faculty of Medicine, University of OttawaDepartment of Health Sciences, Carleton UniversityDepartment of Cellular and Molecular Medicine, Faculty of Medicine, University of OttawaOne 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.https://doi.org/10.1038/s41467-020-15971-w
spellingShingle 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
Nature Communications
title 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_short 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
url https://doi.org/10.1038/s41467-020-15971-w
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