Novel Anti-fibrotic Therapies

Fibrosis is a major player in cardiovascular disease, both as a contributor to the development of disease, as well as a post-injury response that drives progression. Despite the identification of many mechanisms responsible for cardiovascular fibrosis, to date no treatments have emerged that have ef...

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Main Authors: Benita L. McVicker, Robert G. Bennett
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-05-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fphar.2017.00318/full
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spelling doaj-3bfa2c63423c4b02ad8ff33cf3630e822020-11-24T22:51:25ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122017-05-01810.3389/fphar.2017.00318263650Novel Anti-fibrotic TherapiesBenita L. McVicker0Benita L. McVicker1Robert G. Bennett2Robert G. Bennett3Robert G. Bennett4Research Service, VA Nebraska-Western Iowa Health Care System, OmahaNE, United StatesDivision of Gastroenterology and Hepatology, University of Nebraska Medical Center, OmahaNE, United StatesResearch Service, VA Nebraska-Western Iowa Health Care System, OmahaNE, United StatesThe Division of Diabetes, Endocrinology, and Metabolism, Department of Internal Medicine, University of Nebraska Medical Center, OmahaNE, United StatesDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, OmahaNE, United StatesFibrosis is a major player in cardiovascular disease, both as a contributor to the development of disease, as well as a post-injury response that drives progression. Despite the identification of many mechanisms responsible for cardiovascular fibrosis, to date no treatments have emerged that have effectively reduced the excess deposition of extracellular matrix associated with fibrotic conditions. Novel treatments have recently been identified that hold promise as potential therapeutic agents for cardiovascular diseases associated with fibrosis, as well as other fibrotic conditions. The purpose of this review is to provide an overview of emerging antifibrotic agents that have shown encouraging results in preclinical or early clinical studies, but have not yet been approved for use in human disease. One of these agents is bone morphogenetic protein-7 (BMP7), which has beneficial effects in multiple models of fibrotic disease. Another approach discussed involves altering the levels of micro-RNA (miR) species, including miR-29 and miR-101, which regulate the expression of fibrosis-related gene targets. Further, the antifibrotic potential of agonists of the peroxisome proliferator-activated receptors will be discussed. Finally, evidence will be reviewed in support of the polypeptide hormone relaxin. Relaxin is long known for its extracellular remodeling properties in pregnancy, and is rapidly emerging as an effective antifibrotic agent in a number of organ systems. Moreover, relaxin has potent vascular and renal effects that make it a particularly attractive approach for the treatment of cardiovascular diseases. In each case, the mechanism of action and the applicability to various fibrotic diseases will be discussed.http://journal.frontiersin.org/article/10.3389/fphar.2017.00318/fullfibrosiscardiovascular diseaseantifibrotic agentsbone morphogenic protein-7micro-RNArelaxin
collection DOAJ
language English
format Article
sources DOAJ
author Benita L. McVicker
Benita L. McVicker
Robert G. Bennett
Robert G. Bennett
Robert G. Bennett
spellingShingle Benita L. McVicker
Benita L. McVicker
Robert G. Bennett
Robert G. Bennett
Robert G. Bennett
Novel Anti-fibrotic Therapies
Frontiers in Pharmacology
fibrosis
cardiovascular disease
antifibrotic agents
bone morphogenic protein-7
micro-RNA
relaxin
author_facet Benita L. McVicker
Benita L. McVicker
Robert G. Bennett
Robert G. Bennett
Robert G. Bennett
author_sort Benita L. McVicker
title Novel Anti-fibrotic Therapies
title_short Novel Anti-fibrotic Therapies
title_full Novel Anti-fibrotic Therapies
title_fullStr Novel Anti-fibrotic Therapies
title_full_unstemmed Novel Anti-fibrotic Therapies
title_sort novel anti-fibrotic therapies
publisher Frontiers Media S.A.
series Frontiers in Pharmacology
issn 1663-9812
publishDate 2017-05-01
description Fibrosis is a major player in cardiovascular disease, both as a contributor to the development of disease, as well as a post-injury response that drives progression. Despite the identification of many mechanisms responsible for cardiovascular fibrosis, to date no treatments have emerged that have effectively reduced the excess deposition of extracellular matrix associated with fibrotic conditions. Novel treatments have recently been identified that hold promise as potential therapeutic agents for cardiovascular diseases associated with fibrosis, as well as other fibrotic conditions. The purpose of this review is to provide an overview of emerging antifibrotic agents that have shown encouraging results in preclinical or early clinical studies, but have not yet been approved for use in human disease. One of these agents is bone morphogenetic protein-7 (BMP7), which has beneficial effects in multiple models of fibrotic disease. Another approach discussed involves altering the levels of micro-RNA (miR) species, including miR-29 and miR-101, which regulate the expression of fibrosis-related gene targets. Further, the antifibrotic potential of agonists of the peroxisome proliferator-activated receptors will be discussed. Finally, evidence will be reviewed in support of the polypeptide hormone relaxin. Relaxin is long known for its extracellular remodeling properties in pregnancy, and is rapidly emerging as an effective antifibrotic agent in a number of organ systems. Moreover, relaxin has potent vascular and renal effects that make it a particularly attractive approach for the treatment of cardiovascular diseases. In each case, the mechanism of action and the applicability to various fibrotic diseases will be discussed.
topic fibrosis
cardiovascular disease
antifibrotic agents
bone morphogenic protein-7
micro-RNA
relaxin
url http://journal.frontiersin.org/article/10.3389/fphar.2017.00318/full
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