Humanitas Clinical and Research Center, Rozzano (MI), 20098, Italy.
Basic Res Cardiol. 2013 Jul;108(4):361. doi: 10.1007/s00395-013-0361-1. Epub 2013 Jun 6.
Heart failure is a syndrome resulting from a complex genetic predisposition and multiple environmental factors, and is a leading cause of morbidity and mortality. It is frequently accompanied by changes in heart mass, size, and shape, a process known as pathological cardiac remodeling. At the molecular level, these changes are preceded and accompanied by a specific gene expression program characterized by expression of certain 'fetal' genes. This re-expression of fetal genes in the adult heart contributes to the development of the syndrome. Therefore, counteracting the gene expression changes occurring in heart failure could be a therapeutic approach for this pathology. One mechanism of gene expression regulation that has gained importance is epigenetics. This review gives an overview of the roles of some epigenetic mechanisms, such as DNA methylation, histone modifications, ATP-dependent chromatin remodeling, and microRNA-dependent mechanisms, in heart failure.
心力衰竭是一种由复杂的遗传易感性和多种环境因素引起的综合征,是发病率和死亡率的主要原因。它常伴有心脏质量、大小和形状的变化,这个过程被称为病理性心脏重构。在分子水平上,这些变化之前和之后伴随着一个特定的基因表达程序,其特征是某些“胎儿”基因的表达。这些在成人心脏中重新表达的胎儿基因有助于该综合征的发展。因此,对抗心力衰竭中发生的基因表达变化可能是治疗这种疾病的一种方法。基因表达调控的一种机制是表观遗传学。这篇综述概述了一些表观遗传机制的作用,如 DNA 甲基化、组蛋白修饰、ATP 依赖性染色质重塑和 miRNA 依赖性机制在心力衰竭中的作用。