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Roles of MicroRNAs in Bone Destruction of Rheumatoid Arthritis

As an important pathological result of rheumatoid arthritis (RA), bone destruction will lead to joint injury and dysfunction. The imbalance of bone metabolism caused by increased osteoclast activities and decreased osteoblast activities is the main cause of bone destruction in RA. MicroRNAs (MiRNAs)...

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Autores principales: Zhao, Hanxiao, Lu, Aiping, He, Xiaojuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710907/
https://www.ncbi.nlm.nih.gov/pubmed/33330493
http://dx.doi.org/10.3389/fcell.2020.600867
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author Zhao, Hanxiao
Lu, Aiping
He, Xiaojuan
author_facet Zhao, Hanxiao
Lu, Aiping
He, Xiaojuan
author_sort Zhao, Hanxiao
collection PubMed
description As an important pathological result of rheumatoid arthritis (RA), bone destruction will lead to joint injury and dysfunction. The imbalance of bone metabolism caused by increased osteoclast activities and decreased osteoblast activities is the main cause of bone destruction in RA. MicroRNAs (MiRNAs) play an important role in regulating bone metabolic network. Recent studies have shown that miRNAs play indispensable roles in the occurrence and development of bone-related diseases including RA. In this paper, the role of miRNAs in regulating bone destruction of RA in recent years, especially the differentiation and activities of osteoclast and osteoblast, is reviewed. Our results will not only help provide ideas for further studies on miRNAs’ roles in regulating bone destruction, but give candidate targets for miRNAs-based drugs research in bone destruction therapy of RA as well.
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spelling pubmed-77109072020-12-15 Roles of MicroRNAs in Bone Destruction of Rheumatoid Arthritis Zhao, Hanxiao Lu, Aiping He, Xiaojuan Front Cell Dev Biol Cell and Developmental Biology As an important pathological result of rheumatoid arthritis (RA), bone destruction will lead to joint injury and dysfunction. The imbalance of bone metabolism caused by increased osteoclast activities and decreased osteoblast activities is the main cause of bone destruction in RA. MicroRNAs (MiRNAs) play an important role in regulating bone metabolic network. Recent studies have shown that miRNAs play indispensable roles in the occurrence and development of bone-related diseases including RA. In this paper, the role of miRNAs in regulating bone destruction of RA in recent years, especially the differentiation and activities of osteoclast and osteoblast, is reviewed. Our results will not only help provide ideas for further studies on miRNAs’ roles in regulating bone destruction, but give candidate targets for miRNAs-based drugs research in bone destruction therapy of RA as well. Frontiers Media S.A. 2020-11-19 /pmc/articles/PMC7710907/ /pubmed/33330493 http://dx.doi.org/10.3389/fcell.2020.600867 Text en Copyright © 2020 Zhao, Lu and He. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Zhao, Hanxiao
Lu, Aiping
He, Xiaojuan
Roles of MicroRNAs in Bone Destruction of Rheumatoid Arthritis
title Roles of MicroRNAs in Bone Destruction of Rheumatoid Arthritis
title_full Roles of MicroRNAs in Bone Destruction of Rheumatoid Arthritis
title_fullStr Roles of MicroRNAs in Bone Destruction of Rheumatoid Arthritis
title_full_unstemmed Roles of MicroRNAs in Bone Destruction of Rheumatoid Arthritis
title_short Roles of MicroRNAs in Bone Destruction of Rheumatoid Arthritis
title_sort roles of micrornas in bone destruction of rheumatoid arthritis
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710907/
https://www.ncbi.nlm.nih.gov/pubmed/33330493
http://dx.doi.org/10.3389/fcell.2020.600867
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