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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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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. |
format | Online Article Text |
id | pubmed-5703866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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