miRNAs as Therapeutic Targets in Ischemic Heart Disease

被引:60
作者
Frost, Robert J. A. [2 ]
van Rooij, Eva [1 ]
机构
[1] MiRagen Therapeut Inc, Boulder, CO 80301 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
关键词
MicroRNA; Ischemic Heart Disease; Therapeutic Oligonucleotide Chemistries; ISCHEMIA/REPERFUSION INJURY; CARDIAC-HYPERTROPHY; MICRORNA EXPRESSION; IN-VIVO; HYPOXIA; ANGIOGENESIS; APOPTOSIS; RESPONSES; SURVIVAL; REVEALS;
D O I
10.1007/s12265-010-9173-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ischemic heart disease is a form of congestive heart failure that is caused by insufficient blood supply to the heart, resulting in a loss of viable tissue. In response to the injury, the non-ischemic myocardium displays signs of secondary remodeling, like interstitial fibrosis and hypertrophy of cardiac myocytes. This remodeling process further deteriorates pump function and increases susceptibility to arrhythmias. MicroRNAs (miRNAs) are small, non-coding RNAs that regulate gene expression in a sequence-dependent manner. Recently, several groups identified miRNAs as crucial gene regulators in response to myocardial infarction (MI) and during post-MI remodeling. In this review, we discuss how modulation of these miRNAs represents a promising new therapeutic strategy to improve the clinical outcome in ischemic heart disease.
引用
收藏
页码:280 / 289
页数:10
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