不同心力衰竭表型的表观遗传修饰

Alex, er E. Berezin
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引用次数: 4

摘要

心衰(HF)仍然是已知心血管疾病患者死亡的主要原因。在过去的二十年里,有证据表明,在发达国家,新诊断的HF伴射血分数降低(HFrEF)的病例有所减少,而伴射血分数保持(HFpEF)的新诊断频率却显著上升。表观遗传修饰被认为是对靶细胞基因表达中与遗传变化相关的非DNA序列的修饰。表观遗传修饰影响多种分子机制,即DNA甲基化和去乙酰化,atp依赖性染色质重塑,组蛋白修饰和microRNA调节。这篇简短的评论澄清了表观遗传修饰在不同HF表型发育中的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epigenetic Modifications the Development of Different Heart Failure Phenotypes
Heart failure (HF) remains a leading cause of death in patient population with known cardiovascular disease. Within last two decades there are evidences regarding decline to determine newel cases with HF with reduced ejection fraction (HFrEF) in developed countries, whereas the frequency of newly-diagnosed HF with preserved ejection fraction (HFpEF) exhibits dramatically rise. Epigenetic modification is considered a modification of the non- DNA sequences related heritable changes in gene expression of target cells. Epigenetic modifications affect several molecular mechanisms, i.e., DNA methylation and deactylation, ATP-dependent chromatin remodeling, histone modifications, and microRNA regulation. The short commentary is clarified the implication of epigenetic modifications in development of different HF phenotypes.
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