坏死性下垂
上睑下垂
表观遗传学
程序性细胞死亡
组蛋白
DNA甲基化
神经发生的表观遗传调控
生物
细胞凋亡
细胞生物学
组蛋白甲基转移酶
基因表达
遗传学
基因
作者
Cong Chen,Jie Wang,Shan Zhang,Xueying Zhu,Jun Hu,Chao Liu,Lanchun Liu
出处
期刊:Redox biology
[Elsevier BV]
日期:2024-08-19
卷期号:76: 103321-103321
被引量:25
标识
DOI:10.1016/j.redox.2024.103321
摘要
Cell death constitutes a critical component of the pathophysiology of cardiovascular diseases. A growing array of non-apoptotic forms of regulated cell death (RCD)-such as necroptosis, ferroptosis, pyroptosis, and cuproptosis-has been identified and is intimately linked to various cardiovascular conditions. These forms of RCD are governed by genetically programmed mechanisms within the cell, with epigenetic modifications being a common and crucial regulatory method. Such modifications include DNA methylation, RNA methylation, histone methylation, histone acetylation, and non-coding RNAs. This review recaps the roles of DNA methylation, RNA methylation, histone modifications, and non-coding RNAs in cardiovascular diseases, as well as the mechanisms by which epigenetic modifications regulate key proteins involved in cell death. Furthermore, we systematically catalog the existing epigenetic pharmacological agents targeting novel forms of RCD and their mechanisms of action in cardiovascular diseases. This article aims to underscore the pivotal role of epigenetic modifications in precisely regulating specific pathways of novel RCD in cardiovascular diseases, thus offering potential new therapeutic avenues that may prove more effective and safer than traditional treatments.
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