MicroRNAs and myocardial infarction

被引:37
作者
D'Alessandra, Yuri [2 ]
Pompilio, Giulio [2 ,3 ]
Capogrossi, Maurizio C. [1 ]
机构
[1] Ist Dermopat Immacolata IRCCS, Lab Patol Vascolare, I-00167 Rome, Italy
[2] Ctr Cardiol Monzino IRCCS, Lab Biol Vasc & Med Rigenerat, Milan, Italy
[3] Univ Milan, Dipartimento Sci Cardiovasc, Milan, Italy
关键词
biomarkers; miRNA; myocardial infarction; reperfusion injury; ISCHEMIA-REPERFUSION INJURY; EMBRYONIC STEM-CELLS; CARDIOVASCULAR-DISEASE; CIRCULATING MICRORNAS; DOWN-REGULATION; CARDIAC-HYPERTROPHY; TROPONIN ELEVATION; PROGENITOR CELLS; EXPRESSION; DIFFERENTIATION;
D O I
10.1097/HCO.0b013e3283522052
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review We will review the role of microRNAs (miRNAs), small noncoding RNAs with regulatory function, in myocardial infarction (MI). Specifically, we will examine the effect of MI on miRNAs' expression in the heart, the effect of MI on circulating miRNAs, which miRNAs' overexpression or downmodulation appears to have a therapeutic role in MI and which cardiac miRNAs are modulated by drugs/experimental molecules/cell transplantation strategies which have an established or potential therapeutic role in MI. Recent findings A rapidly increasing number of studies are showing that cardiac and circulating miRNAs are markedly altered in MI. These novel findings shed new light on the mechanisms that lead to MI complications, post-MI ventricular remodeling and cardiac repair. Further, recent studies show that circulating miRNAs may represent novel and sensitive biomarkers of MI and, possibly, also an intercellular signaling mechanism. Overexpression and downregulation of specific miRNAs are being evaluated as a novel approach to the treatment of MI. Finally, it appears that some established and potential MI therapies (approved drugs/experimental molecules/cell therapy interventions) may act, at least in part, via modulation of specific miRNAs. Summary Although miRNAs' role in MI is still largely uncharacterized, recent studies suggest that miRNAs may represent novel therapeutic targets and MI biomarkers.
引用
收藏
页码:228 / 235
页数:8
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