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Research Progress of Fibroblast Growth Factor 21 in Fibrotic Diseases

Fibrosis is a common pathological outcome of chronic injuries, characterized by excessive deposition of extracellular matrix components in organs, as seen in most chronic inflammatory diseases. At present, there is an increasing tendency of the morbidity and mortality of diseases caused by fibrosis,...

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Detalles Bibliográficos
Autores principales: Jia, Min-Qi, Guan, Cha-Xiang, Tao, Jia-Hao, Zhou, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168133/
https://www.ncbi.nlm.nih.gov/pubmed/35677107
http://dx.doi.org/10.1155/2022/5042762
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author Jia, Min-Qi
Guan, Cha-Xiang
Tao, Jia-Hao
Zhou, Yong
author_facet Jia, Min-Qi
Guan, Cha-Xiang
Tao, Jia-Hao
Zhou, Yong
author_sort Jia, Min-Qi
collection PubMed
description Fibrosis is a common pathological outcome of chronic injuries, characterized by excessive deposition of extracellular matrix components in organs, as seen in most chronic inflammatory diseases. At present, there is an increasing tendency of the morbidity and mortality of diseases caused by fibrosis, but the treatment measures for fibrosis are still limited. Fibroblast growth factor 21 (FGF21) belongs to the FGF19 subfamily, which also has the name endocrine FGFs because of their endocrine manner. In recent years, it has been found that plasma FGF21 level is significantly correlated with fibrosis progression. Furthermore, there is evidence that FGF21 has a pronounced antifibrotic effect in a variety of fibrotic diseases. This review summarizes the biological effects of FGF21 and discusses what is currently known about this factor and fibrosis disease, highlighting emerging insights that warrant further research.
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spelling pubmed-91681332022-06-07 Research Progress of Fibroblast Growth Factor 21 in Fibrotic Diseases Jia, Min-Qi Guan, Cha-Xiang Tao, Jia-Hao Zhou, Yong Oxid Med Cell Longev Review Article Fibrosis is a common pathological outcome of chronic injuries, characterized by excessive deposition of extracellular matrix components in organs, as seen in most chronic inflammatory diseases. At present, there is an increasing tendency of the morbidity and mortality of diseases caused by fibrosis, but the treatment measures for fibrosis are still limited. Fibroblast growth factor 21 (FGF21) belongs to the FGF19 subfamily, which also has the name endocrine FGFs because of their endocrine manner. In recent years, it has been found that plasma FGF21 level is significantly correlated with fibrosis progression. Furthermore, there is evidence that FGF21 has a pronounced antifibrotic effect in a variety of fibrotic diseases. This review summarizes the biological effects of FGF21 and discusses what is currently known about this factor and fibrosis disease, highlighting emerging insights that warrant further research. Hindawi 2022-05-29 /pmc/articles/PMC9168133/ /pubmed/35677107 http://dx.doi.org/10.1155/2022/5042762 Text en Copyright © 2022 Min-Qi Jia et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Jia, Min-Qi
Guan, Cha-Xiang
Tao, Jia-Hao
Zhou, Yong
Research Progress of Fibroblast Growth Factor 21 in Fibrotic Diseases
title Research Progress of Fibroblast Growth Factor 21 in Fibrotic Diseases
title_full Research Progress of Fibroblast Growth Factor 21 in Fibrotic Diseases
title_fullStr Research Progress of Fibroblast Growth Factor 21 in Fibrotic Diseases
title_full_unstemmed Research Progress of Fibroblast Growth Factor 21 in Fibrotic Diseases
title_short Research Progress of Fibroblast Growth Factor 21 in Fibrotic Diseases
title_sort research progress of fibroblast growth factor 21 in fibrotic diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168133/
https://www.ncbi.nlm.nih.gov/pubmed/35677107
http://dx.doi.org/10.1155/2022/5042762
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