乙酰化
组蛋白
组蛋白脱乙酰基酶
医学
疾病
酶
药理学
癌症研究
生物信息学
生物
基因
生物化学
内科学
作者
Vikas Tiwari,S. K. Banerjee
出处
期刊:Current Drug Targets
[Bentham Science]
日期:2022-10-05
卷期号:24 (9): 718-727
被引量:2
标识
DOI:10.2174/1389450123666221003094908
摘要
Protein acetylation is a reversible central mechanism to control gene expression and cell signaling events. Current evidence suggests that pharmacological inhibitors for protein deacetylation have already been used in various disease conditions. Accumulating reports showed that several compounds that enhance histone acetylation in cells are in both the preclinical and clinical development stages targeting non-communicable diseases, which include cancerous and non-cancerous especially cardiovascular complications. These compounds are, in general, enzyme inhibitors and target a family of enzymes- called histone deacetylases (HDACs). Since HDAC inhibitors have shown to be helpful in preclinical models of cardiac complications, further research on developing novel compounds with high efficacy and low toxicity may be essential for treating cardiovascular diseases. In this review, we have highlighted the roles of HDAC and its inhibitors in cardiac complications.
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