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Endostatin in fibrosis and as a potential candidate of anti-fibrotic therapy
Fibrotic diseases pose significant clinical challenges due to their broadness and complexity. Thus, a better understanding of fibrogenesis and the development of more effective treatments is imperative. Recent evidence suggests a significant antifibrotic potential of an endogenous glycoprotein, endo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491667/ https://www.ncbi.nlm.nih.gov/pubmed/34595978 http://dx.doi.org/10.1080/10717544.2021.1983071 |
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author | Zhang, Zequn Liu, Xi Shen, Zhaolong Quan, Jun Lin, Changwei Li, Xiaorong Hu, Gui |
author_facet | Zhang, Zequn Liu, Xi Shen, Zhaolong Quan, Jun Lin, Changwei Li, Xiaorong Hu, Gui |
author_sort | Zhang, Zequn |
collection | PubMed |
description | Fibrotic diseases pose significant clinical challenges due to their broadness and complexity. Thus, a better understanding of fibrogenesis and the development of more effective treatments is imperative. Recent evidence suggests a significant antifibrotic potential of an endogenous glycoprotein, endostatin. While endostatin has been widely studied for its role as an anticancer adjuvant by inhibiting tumor angiogenesis, its possible implication in fibrosis remains largely unclear. Here, we review the role of endostatin in various cellular processes and highlight its antifibrotic activity. We hypothesize that endostatin conveys a homeostatic function in the process of fibrosis by regulating (a) TGF-β1 and its downstream signaling; (b) RhoA/ROCK pathway; (c) NF-κB signaling pathway; (d) expression of EGR-1; (e) PDGF/PDGFR pathway; (f) autophagy-related pathways; (g) pathways associated with cell proliferation and apoptosis. Finally, we propose a schematic model of the antifibrotic roles and mechanisms of endostatin; also, we outline future research directions of endostatin and aim to present a potential therapeutic approach for fibrosis. |
format | Online Article Text |
id | pubmed-8491667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-84916672021-10-06 Endostatin in fibrosis and as a potential candidate of anti-fibrotic therapy Zhang, Zequn Liu, Xi Shen, Zhaolong Quan, Jun Lin, Changwei Li, Xiaorong Hu, Gui Drug Deliv Research Article Fibrotic diseases pose significant clinical challenges due to their broadness and complexity. Thus, a better understanding of fibrogenesis and the development of more effective treatments is imperative. Recent evidence suggests a significant antifibrotic potential of an endogenous glycoprotein, endostatin. While endostatin has been widely studied for its role as an anticancer adjuvant by inhibiting tumor angiogenesis, its possible implication in fibrosis remains largely unclear. Here, we review the role of endostatin in various cellular processes and highlight its antifibrotic activity. We hypothesize that endostatin conveys a homeostatic function in the process of fibrosis by regulating (a) TGF-β1 and its downstream signaling; (b) RhoA/ROCK pathway; (c) NF-κB signaling pathway; (d) expression of EGR-1; (e) PDGF/PDGFR pathway; (f) autophagy-related pathways; (g) pathways associated with cell proliferation and apoptosis. Finally, we propose a schematic model of the antifibrotic roles and mechanisms of endostatin; also, we outline future research directions of endostatin and aim to present a potential therapeutic approach for fibrosis. Taylor & Francis 2021-10-01 /pmc/articles/PMC8491667/ /pubmed/34595978 http://dx.doi.org/10.1080/10717544.2021.1983071 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhang, Zequn Liu, Xi Shen, Zhaolong Quan, Jun Lin, Changwei Li, Xiaorong Hu, Gui Endostatin in fibrosis and as a potential candidate of anti-fibrotic therapy |
title | Endostatin in fibrosis and as a potential candidate of anti-fibrotic therapy |
title_full | Endostatin in fibrosis and as a potential candidate of anti-fibrotic therapy |
title_fullStr | Endostatin in fibrosis and as a potential candidate of anti-fibrotic therapy |
title_full_unstemmed | Endostatin in fibrosis and as a potential candidate of anti-fibrotic therapy |
title_short | Endostatin in fibrosis and as a potential candidate of anti-fibrotic therapy |
title_sort | endostatin in fibrosis and as a potential candidate of anti-fibrotic therapy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491667/ https://www.ncbi.nlm.nih.gov/pubmed/34595978 http://dx.doi.org/10.1080/10717544.2021.1983071 |
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