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Antimyostatin Treatment in Health and Disease: The Story of Great Expectations and Limited Success

In the past 20 years, myostatin, a negative regulator of muscle mass, has attracted attention as a potential therapeutic target in muscular dystrophies and other conditions. Preclinical studies have shown potential for increasing muscular mass and ameliorating the pathological features of dystrophic...

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Detalles Bibliográficos
Autores principales: Nielsen, Tue L., Vissing, John, Krag, Thomas O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001237/
https://www.ncbi.nlm.nih.gov/pubmed/33802348
http://dx.doi.org/10.3390/cells10030533
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author Nielsen, Tue L.
Vissing, John
Krag, Thomas O.
author_facet Nielsen, Tue L.
Vissing, John
Krag, Thomas O.
author_sort Nielsen, Tue L.
collection PubMed
description In the past 20 years, myostatin, a negative regulator of muscle mass, has attracted attention as a potential therapeutic target in muscular dystrophies and other conditions. Preclinical studies have shown potential for increasing muscular mass and ameliorating the pathological features of dystrophic muscle by the inhibition of myostatin in various ways. However, hardly any clinical trials have proven to translate the promising results from the animal models into patient populations. We present the background for myostatin regulation, clinical and preclinical results and discuss why translation from animal models to patients is difficult. Based on this, we put the clinical relevance of future antimyostatin treatment into perspective.
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spelling pubmed-80012372021-03-28 Antimyostatin Treatment in Health and Disease: The Story of Great Expectations and Limited Success Nielsen, Tue L. Vissing, John Krag, Thomas O. Cells Review In the past 20 years, myostatin, a negative regulator of muscle mass, has attracted attention as a potential therapeutic target in muscular dystrophies and other conditions. Preclinical studies have shown potential for increasing muscular mass and ameliorating the pathological features of dystrophic muscle by the inhibition of myostatin in various ways. However, hardly any clinical trials have proven to translate the promising results from the animal models into patient populations. We present the background for myostatin regulation, clinical and preclinical results and discuss why translation from animal models to patients is difficult. Based on this, we put the clinical relevance of future antimyostatin treatment into perspective. MDPI 2021-03-03 /pmc/articles/PMC8001237/ /pubmed/33802348 http://dx.doi.org/10.3390/cells10030533 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Review
Nielsen, Tue L.
Vissing, John
Krag, Thomas O.
Antimyostatin Treatment in Health and Disease: The Story of Great Expectations and Limited Success
title Antimyostatin Treatment in Health and Disease: The Story of Great Expectations and Limited Success
title_full Antimyostatin Treatment in Health and Disease: The Story of Great Expectations and Limited Success
title_fullStr Antimyostatin Treatment in Health and Disease: The Story of Great Expectations and Limited Success
title_full_unstemmed Antimyostatin Treatment in Health and Disease: The Story of Great Expectations and Limited Success
title_short Antimyostatin Treatment in Health and Disease: The Story of Great Expectations and Limited Success
title_sort antimyostatin treatment in health and disease: the story of great expectations and limited success
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001237/
https://www.ncbi.nlm.nih.gov/pubmed/33802348
http://dx.doi.org/10.3390/cells10030533
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