HDAC inhibitors as antifibrotic drugs in cardiac and pulmonary fibrosis

Fibrosis usually results from dysregulated wound repair and is characterized by excessive scar tissue. It is a complex process with unclear mechanisms. Accumulating evidence indicates that epigenetic alterations, including histone acetylation, play a pivotal role in this process. Histone acetylation...

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Main Authors: Xing Lyu, Min Hu, Jieting Peng, Xiangyu Zhang, Yan Y Sanders
Format: Article
Language:English
Published: SAGE Publishing 2019-07-01
Series:Therapeutic Advances in Chronic Disease
Online Access:https://doi.org/10.1177/2040622319862697
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author Xing Lyu
Min Hu
Jieting Peng
Xiangyu Zhang
Yan Y Sanders
author_facet Xing Lyu
Min Hu
Jieting Peng
Xiangyu Zhang
Yan Y Sanders
author_sort Xing Lyu
collection DOAJ
description Fibrosis usually results from dysregulated wound repair and is characterized by excessive scar tissue. It is a complex process with unclear mechanisms. Accumulating evidence indicates that epigenetic alterations, including histone acetylation, play a pivotal role in this process. Histone acetylation is governed by histone acetyltransferases (HATs) and histone deacetylases (HDACs). HDACs are enzymes that remove the acetyl groups from both histone and nonhistone proteins. Aberrant HDAC activities are observed in fibrotic diseases, including cardiac and pulmonary fibrosis. HDAC inhibitors (HDACIs) are molecules that block HDAC functions. HDACIs have been studied extensively in a variety of tumors. Currently, there are four HDACIs approved by the US Food and Drug Administration for cancer treatment yet none for fibrotic diseases. Emerging evidence from in vitro and in vivo preclinical studies has presented beneficial effects of HDACIs in preventing or reversing fibrogenesis. In this review, we summarize the latest findings of the roles of HDACs in the pathogenesis of cardiac and pulmonary fibrosis and highlight the potential applications of HDACIs in these two fibrotic diseases.
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spelling doaj.art-2fa325bb3d3343fb99c53a72af0c20312022-12-21T19:56:45ZengSAGE PublishingTherapeutic Advances in Chronic Disease2040-62312019-07-011010.1177/2040622319862697HDAC inhibitors as antifibrotic drugs in cardiac and pulmonary fibrosisXing LyuMin HuJieting PengXiangyu ZhangYan Y SandersFibrosis usually results from dysregulated wound repair and is characterized by excessive scar tissue. It is a complex process with unclear mechanisms. Accumulating evidence indicates that epigenetic alterations, including histone acetylation, play a pivotal role in this process. Histone acetylation is governed by histone acetyltransferases (HATs) and histone deacetylases (HDACs). HDACs are enzymes that remove the acetyl groups from both histone and nonhistone proteins. Aberrant HDAC activities are observed in fibrotic diseases, including cardiac and pulmonary fibrosis. HDAC inhibitors (HDACIs) are molecules that block HDAC functions. HDACIs have been studied extensively in a variety of tumors. Currently, there are four HDACIs approved by the US Food and Drug Administration for cancer treatment yet none for fibrotic diseases. Emerging evidence from in vitro and in vivo preclinical studies has presented beneficial effects of HDACIs in preventing or reversing fibrogenesis. In this review, we summarize the latest findings of the roles of HDACs in the pathogenesis of cardiac and pulmonary fibrosis and highlight the potential applications of HDACIs in these two fibrotic diseases.https://doi.org/10.1177/2040622319862697
spellingShingle Xing Lyu
Min Hu
Jieting Peng
Xiangyu Zhang
Yan Y Sanders
HDAC inhibitors as antifibrotic drugs in cardiac and pulmonary fibrosis
Therapeutic Advances in Chronic Disease
title HDAC inhibitors as antifibrotic drugs in cardiac and pulmonary fibrosis
title_full HDAC inhibitors as antifibrotic drugs in cardiac and pulmonary fibrosis
title_fullStr HDAC inhibitors as antifibrotic drugs in cardiac and pulmonary fibrosis
title_full_unstemmed HDAC inhibitors as antifibrotic drugs in cardiac and pulmonary fibrosis
title_short HDAC inhibitors as antifibrotic drugs in cardiac and pulmonary fibrosis
title_sort hdac inhibitors as antifibrotic drugs in cardiac and pulmonary fibrosis
url https://doi.org/10.1177/2040622319862697
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