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Drugs and Targets in Fibrosis

Fibrosis contributes to the development of many diseases and many target molecules are involved in fibrosis. Currently, the majority of fibrosis treatment strategies are limited to specific diseases or organs. However, accumulating evidence demonstrates great similarities among fibroproliferative di...

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Detalles Bibliográficos
Autores principales: Li, Xiaoyi, Zhu, Lixin, Wang, Beibei, Yuan, Meifei, Zhu, Ruixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703866/
https://www.ncbi.nlm.nih.gov/pubmed/29218009
http://dx.doi.org/10.3389/fphar.2017.00855
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author Li, Xiaoyi
Zhu, Lixin
Wang, Beibei
Yuan, Meifei
Zhu, Ruixin
author_facet Li, Xiaoyi
Zhu, Lixin
Wang, Beibei
Yuan, Meifei
Zhu, Ruixin
author_sort Li, Xiaoyi
collection PubMed
description Fibrosis contributes to the development of many diseases and many target molecules are involved in fibrosis. Currently, the majority of fibrosis treatment strategies are limited to specific diseases or organs. However, accumulating evidence demonstrates great similarities among fibroproliferative diseases, and more and more drugs are proved to be effective anti-fibrotic therapies across different diseases and organs. Here we comprehensively review the current knowledge on the pathological mechanisms of fibrosis, and divide factors mediating fibrosis progression into extracellular and intracellular groups. Furthermore, we systematically summarize both single and multiple component drugs that target fibrosis. Future directions of fibrosis drug discovery are also proposed.
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spelling pubmed-57038662017-12-07 Drugs and Targets in Fibrosis Li, Xiaoyi Zhu, Lixin Wang, Beibei Yuan, Meifei Zhu, Ruixin Front Pharmacol Pharmacology Fibrosis contributes to the development of many diseases and many target molecules are involved in fibrosis. Currently, the majority of fibrosis treatment strategies are limited to specific diseases or organs. However, accumulating evidence demonstrates great similarities among fibroproliferative diseases, and more and more drugs are proved to be effective anti-fibrotic therapies across different diseases and organs. Here we comprehensively review the current knowledge on the pathological mechanisms of fibrosis, and divide factors mediating fibrosis progression into extracellular and intracellular groups. Furthermore, we systematically summarize both single and multiple component drugs that target fibrosis. Future directions of fibrosis drug discovery are also proposed. Frontiers Media S.A. 2017-11-23 /pmc/articles/PMC5703866/ /pubmed/29218009 http://dx.doi.org/10.3389/fphar.2017.00855 Text en Copyright © 2017 Li, Zhu, Wang, Yuan and Zhu. 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) or licensor 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 Pharmacology
Li, Xiaoyi
Zhu, Lixin
Wang, Beibei
Yuan, Meifei
Zhu, Ruixin
Drugs and Targets in Fibrosis
title Drugs and Targets in Fibrosis
title_full Drugs and Targets in Fibrosis
title_fullStr Drugs and Targets in Fibrosis
title_full_unstemmed Drugs and Targets in Fibrosis
title_short Drugs and Targets in Fibrosis
title_sort drugs and targets in fibrosis
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703866/
https://www.ncbi.nlm.nih.gov/pubmed/29218009
http://dx.doi.org/10.3389/fphar.2017.00855
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