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HDAC4 Inhibitors as Antivascular Senescence Therapeutics

Aging is an inevitable consequence of life, and during this process, the epigenetic landscape changes and reactive oxygen species (ROS) accumulation increases. Inevitably, these changes are common in many age-related diseases, including neurodegeneration, hypertension, and cardiovascular diseases. I...

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Autores principales: Huang, Chuoji, Lin, Zhongxiao, Liu, Xiaoyan, Ding, Qian, Cai, Jianghong, Zhang, Zhongyi, Rose, Peter, Zhu, Yi Zhun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259336/
https://www.ncbi.nlm.nih.gov/pubmed/35814270
http://dx.doi.org/10.1155/2022/3087916
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author Huang, Chuoji
Lin, Zhongxiao
Liu, Xiaoyan
Ding, Qian
Cai, Jianghong
Zhang, Zhongyi
Rose, Peter
Zhu, Yi Zhun
author_facet Huang, Chuoji
Lin, Zhongxiao
Liu, Xiaoyan
Ding, Qian
Cai, Jianghong
Zhang, Zhongyi
Rose, Peter
Zhu, Yi Zhun
author_sort Huang, Chuoji
collection PubMed
description Aging is an inevitable consequence of life, and during this process, the epigenetic landscape changes and reactive oxygen species (ROS) accumulation increases. Inevitably, these changes are common in many age-related diseases, including neurodegeneration, hypertension, and cardiovascular diseases. In the current research, histone deacetylation 4 (HDAC4) was studied as a potential therapeutic target in vascular senescence. HDAC4 is a specific class II histone deacetylation protein that participates in epigenetic modifications and deacetylation of heat shock proteins and various transcription factors. There is increasing evidence to support that HDAC4 is a potential therapeutic target, and developments in the synthesis and testing of HDAC4 inhibitors are now gaining interest from academia and the pharmaceutical industry.
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spelling pubmed-92593362022-07-07 HDAC4 Inhibitors as Antivascular Senescence Therapeutics Huang, Chuoji Lin, Zhongxiao Liu, Xiaoyan Ding, Qian Cai, Jianghong Zhang, Zhongyi Rose, Peter Zhu, Yi Zhun Oxid Med Cell Longev Review Article Aging is an inevitable consequence of life, and during this process, the epigenetic landscape changes and reactive oxygen species (ROS) accumulation increases. Inevitably, these changes are common in many age-related diseases, including neurodegeneration, hypertension, and cardiovascular diseases. In the current research, histone deacetylation 4 (HDAC4) was studied as a potential therapeutic target in vascular senescence. HDAC4 is a specific class II histone deacetylation protein that participates in epigenetic modifications and deacetylation of heat shock proteins and various transcription factors. There is increasing evidence to support that HDAC4 is a potential therapeutic target, and developments in the synthesis and testing of HDAC4 inhibitors are now gaining interest from academia and the pharmaceutical industry. Hindawi 2022-06-29 /pmc/articles/PMC9259336/ /pubmed/35814270 http://dx.doi.org/10.1155/2022/3087916 Text en Copyright © 2022 Chuoji Huang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Huang, Chuoji
Lin, Zhongxiao
Liu, Xiaoyan
Ding, Qian
Cai, Jianghong
Zhang, Zhongyi
Rose, Peter
Zhu, Yi Zhun
HDAC4 Inhibitors as Antivascular Senescence Therapeutics
title HDAC4 Inhibitors as Antivascular Senescence Therapeutics
title_full HDAC4 Inhibitors as Antivascular Senescence Therapeutics
title_fullStr HDAC4 Inhibitors as Antivascular Senescence Therapeutics
title_full_unstemmed HDAC4 Inhibitors as Antivascular Senescence Therapeutics
title_short HDAC4 Inhibitors as Antivascular Senescence Therapeutics
title_sort hdac4 inhibitors as antivascular senescence therapeutics
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259336/
https://www.ncbi.nlm.nih.gov/pubmed/35814270
http://dx.doi.org/10.1155/2022/3087916
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