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Cardiovascular Research Advance Access first published online on July 9, 2008
This version [Corrected Proof] published online on July 22, 2008

Cardiovascular Research, doi:10.1093/cvr/cvn181
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Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2008. For permissions please email: journals.permissions@oxfordjournals.org

Control of cardiac excitability by microRNAs

Baofeng Yang1,2,*, Yanjie Lu1,2 and Zhiguo Wang2,3,4,*

1 Department of Pharmacology (The State-Province Key Laboratories of Biomedicine-Pharmaceutics of China), Harbin Medical University, Harbin, Heilongjiang 150086, P.R. China
2 Cardiovascular Research Institute, Harbin Medical University, Harbin, Heilongjiang 150086, P.R. China
3 Research Center, Montreal Heart Institute, 5000 Belanger East, Montreal, Canada PQ H1T 1C8
4 Department of Medicine, University of Montreal, Montreal, Canada PQ H3C 3J7

* Corresponding authors. Tel: +86 451 8667 9473 (B.Y.) or Tel: +1 514 376 3330; Fax: +1 514 376 4452 (Z.W.) E-mail address: yangbf{at}ems.hrbmu.edu.cn (B.Y.) or wz.email{at}gmail.com (Z.W.)

Cardiovascular disease is the leading cause of morbidity and mortality in developed countries. The pathological process of the heart is associated with an altered expression profile of genes that are important for cardiac function. MicroRNAs (miRNAs) have recently emerged as one of the central players of gene expression regulation. The implications of miRNAs in the pathological process of the cardiovascular system have recently been recognized, and research on miRNAs in relation to cardiovascular disease has now become a most rapidly evolving field. In this review, we focus on miRNAs and control of cardiac excitability, aiming to provide a comprehensive overview on the available experimental data on regulation of cardiac conduction, repolarization, and automaticity by miRNAs. Aberrant expression of miRNAs in the diseased state of the heart and their arrhythmogenic or anti-arrhythmic potential will be discussed. Finally, the innovative miRNA-interference technologies developed lately for manipulating the action of miRNAs by interfering with their expression, stability, and function as new approaches for miRNA research and gene therapy will be introduced.

KEYWORDS miRNA; Arrhythmias; Cardiac excitability; Ion channels; Gene expression


Time for primary review: 25 days


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