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微小 RNA 调控与心脏钙信号:在心脏疾病中的作用和治疗潜力。

MicroRNA regulation and cardiac calcium signaling: role in cardiac disease and therapeutic potential.

机构信息

From the Department of Medicine and Research Center, Montreal Heart Institute and Université de Montréal, Montreal, Quebec, Canada (M.H., X.L., S.N.); Department of Cardiology, Hamamatsu Medical Center, Hamamatsu, Japan (M.H.); Cardiovascular Research Institute and Department of Pharmacology, Harbin Medical University, Harbin, People's Republic of China (X.L.; B.Y.); Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan (T.M.); and Institute of Pharmacology, Faculty of Medicine, University Duisburg-Essen, Essen, Germany (D.D.).

出版信息

Circ Res. 2014 Feb 14;114(4):689-705. doi: 10.1161/CIRCRESAHA.114.301798.

Abstract

MicroRNAs (miRNAs) are emerging as key control molecules in the regulation of gene expression, and their role in heart disease is becoming increasingly evident. Given the critical role of Ca(2+) handling and signaling proteins in the maintenance of cardiac function, the targeting of such proteins by miRNAs would be expected to have important consequences. miRNAs have indeed been shown to control the expression of genes encoding important Ca(2+) handling and signaling proteins, and are themselves regulated by Ca(2+)-dependent processes. Ca(2+)-related miRNAs have been found to be significant pathophysiological contributors in conditions like myocardial ischemic injury, cardiac hypertrophy, heart failure, ventricular arrhythmogenesis, and atrial fibrillation. This review is a comprehensive analysis of the present knowledge concerning miRNA regulation of Ca(2+) handling processes, the participation of Ca(2+)-regulating miRNAs in the evolution of heart disease, the mutual relationship between Ca(2+) signaling and miRNAs in the control of cardiac function, and the potential value of miRNA-control of Ca(2+) handling as a therapeutic target.

摘要

微小 RNA(miRNAs)作为基因表达调控的关键控制分子而崭露头角,其在心脏病中的作用也越来越明显。鉴于 Ca(2+)处理和信号蛋白在维持心脏功能中的关键作用,miRNAs 靶向这些蛋白预计会产生重要的后果。miRNAs 确实可以控制编码重要 Ca(2+)处理和信号蛋白的基因的表达,并且本身也受到 Ca(2+)依赖过程的调节。已经发现与 Ca(2+)相关的 miRNAs 在心肌缺血损伤、心脏肥大、心力衰竭、室性心律失常和心房颤动等情况下是重要的病理生理贡献者。这篇综述是对 miRNA 调节 Ca(2+)处理过程的现有知识的全面分析,Ca(2+)调节 miRNAs 参与心脏病的发生发展,Ca(2+)信号和 miRNAs 在心脏功能控制中的相互关系,以及 miRNA 控制 Ca(2+)处理作为治疗靶点的潜在价值。

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