Cargando…

MicroRNAs in Dystrophinopathy

Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD), which represent the range of dystrophinopathies, account for nearly 80% of muscle dystrophy. DMD and BMD result from the loss of a functional dystrophin protein, and the leading cause of death in these patients is cardiac remodel...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Ahyoung, Moon, Jiwon, Yu, Jin, Kho, Changwon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318410/
https://www.ncbi.nlm.nih.gov/pubmed/35887128
http://dx.doi.org/10.3390/ijms23147785
_version_ 1784755283842564096
author Lee, Ahyoung
Moon, Jiwon
Yu, Jin
Kho, Changwon
author_facet Lee, Ahyoung
Moon, Jiwon
Yu, Jin
Kho, Changwon
author_sort Lee, Ahyoung
collection PubMed
description Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD), which represent the range of dystrophinopathies, account for nearly 80% of muscle dystrophy. DMD and BMD result from the loss of a functional dystrophin protein, and the leading cause of death in these patients is cardiac remodeling and heart failure. The pathogenesis and progression of the more severe form of DMD have been extensively studied and are controlled by many determinants, including microRNAs (miRNAs). The regulatory role of miRNAs in muscle function and the differential miRNA expression in muscular dystrophy indicate the clinical significance of miRNAs. This review discusses the relevant microRNAs as potential biomarkers and therapeutic targets for DMD and DMD cardiomyopathy as examples of dystrophinopathies.
format Online
Article
Text
id pubmed-9318410
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-93184102022-07-27 MicroRNAs in Dystrophinopathy Lee, Ahyoung Moon, Jiwon Yu, Jin Kho, Changwon Int J Mol Sci Review Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD), which represent the range of dystrophinopathies, account for nearly 80% of muscle dystrophy. DMD and BMD result from the loss of a functional dystrophin protein, and the leading cause of death in these patients is cardiac remodeling and heart failure. The pathogenesis and progression of the more severe form of DMD have been extensively studied and are controlled by many determinants, including microRNAs (miRNAs). The regulatory role of miRNAs in muscle function and the differential miRNA expression in muscular dystrophy indicate the clinical significance of miRNAs. This review discusses the relevant microRNAs as potential biomarkers and therapeutic targets for DMD and DMD cardiomyopathy as examples of dystrophinopathies. MDPI 2022-07-14 /pmc/articles/PMC9318410/ /pubmed/35887128 http://dx.doi.org/10.3390/ijms23147785 Text en © 2022 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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lee, Ahyoung
Moon, Jiwon
Yu, Jin
Kho, Changwon
MicroRNAs in Dystrophinopathy
title MicroRNAs in Dystrophinopathy
title_full MicroRNAs in Dystrophinopathy
title_fullStr MicroRNAs in Dystrophinopathy
title_full_unstemmed MicroRNAs in Dystrophinopathy
title_short MicroRNAs in Dystrophinopathy
title_sort micrornas in dystrophinopathy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318410/
https://www.ncbi.nlm.nih.gov/pubmed/35887128
http://dx.doi.org/10.3390/ijms23147785
work_keys_str_mv AT leeahyoung micrornasindystrophinopathy
AT moonjiwon micrornasindystrophinopathy
AT yujin micrornasindystrophinopathy
AT khochangwon micrornasindystrophinopathy