microRNAs in Cardiovascular Diseases Current Knowledge and the Road Ahead

被引:315
作者
Condorelli, Gianluigi [1 ,2 ,3 ]
Latronico, Michael V. G. [1 ]
Cavarretta, Elena [4 ]
机构
[1] Humanitas Res Hosp, Cardiovasc Res Ctr, I-20089 Rozzano, MI, Italy
[2] Univ Milan, Dept Med Biotechnol & Translat Med, Rozzano, Italy
[3] CNR, Inst Genet & Biomed Res, Rome, Italy
[4] Univ Roma La Sapienza, Dept Med Surg Sci & Biotechnol, Latina, Italy
基金
欧洲研究理事会;
关键词
cardiovascular disease; heart disease; microRNA; ACUTE MYOCARDIAL-INFARCTION; CELL PHENOTYPIC SWITCH; SMOOTH-MUSCLE-CELLS; CIRCULATING MICRORNAS; CARDIAC-HYPERTROPHY; MESSENGER-RNAS; BONE-MARROW; INFLAMMATORY RESPONSE; NONCODING RNAS; LIPID UPTAKE;
D O I
10.1016/j.jacc.2014.01.050
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Over the last few years, the field of microribonucleic acid (miRNA) in cardiovascular biology and disease has expanded at an incredible pace. miRNAs are themselves part of a larger family, that of non-coding RNAs, the importance of which for biological processes is starting to emerge. miRNAs are similar to 22-nucleotide-long RNA sequences that can legate messenger (m) RNAs at partially complementary binding sites, and hence regulate the rate of protein synthesis by altering the stability of the targeted mRNAs. In the cardiovascular system, miRNAs have been shown to be critical regulators of development and physiology. They control basic functions in virtually all cell types relevant to the cardiovascular system (such as endothelial cells, cardiac muscle, smooth muscle, inflammatory cells, and fibroblasts) and, thus, are directly involved in the pathophysiology of many cardiovascular diseases. As a result of their role in disease, they are being studied for exploitation in diagnostics, prognostics, and therapeutics. However, there are still significant obstacles that need to be overcome before they enter the clinical arena. We present here a review of the literature and outline the directions toward their use in the clinic. (C) 2014 by the American College of Cardiology Foundation
引用
收藏
页码:2177 / 2187
页数:11
相关论文
共 134 条
[1]
Circulating microRNA-1 as a potential novel biomarker for acute myocardial infarction [J].
Ai, Jing ;
Zhang, Rong ;
Li, Yue ;
Pu, Jielin ;
Lu, Yanjie ;
Jiao, Jundong ;
Li, Kang ;
Yu, Bo ;
Li, Zhuqin ;
Wang, Rongrong ;
Wang, Lihong ;
Li, Qiang ;
Wang, Nina ;
Shan, Hongli ;
Li, Zhongyu ;
Yang, Baofeng .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 391 (01) :73-77
[2]
MicroRNA-126 contributes to renal microvascular heterogeneity of VCAM-1 protein expression in acute inflammation [J].
Asgeirsdottir, S. A. ;
van Solingen, C. ;
Kurniati, N. F. ;
Zwiers, P. J. ;
Heeringa, P. ;
van Meurs, M. ;
Satchell, S. C. ;
Saleem, M. A. ;
Mathieson, P. W. ;
Banas, B. ;
Kamps, J. A. A. M. ;
Rabelink, T. J. ;
van Zonneveld, A. J. ;
Molema, G. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2012, 302 (12) :F1630-F1639
[3]
MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[4]
Circulating miR-133a and miR-423-5p fail as biomarkers for left ventricular remodeling after myocardial infarction [J].
Bauters, Christophe ;
Kumarswamy, Regalla ;
Holzmann, Angelika ;
Bretthauer, Julia ;
Anker, Stefan D. ;
Pinet, Florence ;
Thum, Thomas .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2013, 168 (03) :1837-1840
[5]
Proteomics of plaques and novel sources of potential biomarkers for atherosclerosis [J].
Bleijerveld, Onno B. ;
Zhang, Ya-Nan ;
Beldar, Serap ;
Hoefer, Imo E. ;
Sze, Siu K. ;
Pasterkamp, Gerard ;
de Kleijn, Dominique P. V. .
PROTEOMICS CLINICAL APPLICATIONS, 2013, 7 (7-8) :490-503
[6]
Heparin Selectively Affects the Quantification of MicroRNAs in Human Blood Samples [J].
Boeckel, Jes-Niels ;
Thome, Claudia E. ;
Leistner, David ;
Zeiher, Andreas M. ;
Fichtlscherer, Stephan ;
Dimmeler, Stefanie .
CLINICAL CHEMISTRY, 2013, 59 (07) :1125-1127
[7]
Acquisition of the contractile phenotype by murine arterial smooth muscle cells depends on the Mir143/145 gene cluster [J].
Boettger, Thomas ;
Beetz, Nadine ;
Kostin, Sawa ;
Schneider, Johanna ;
Krueger, Marcus ;
Hein, Lutz ;
Braun, Thomas .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (09) :2634-2647
[8]
MicroRNA-92a Controls Angiogenesis and Functional Recovery of Ischemic Tissues in Mice [J].
Bonauer, Angelika ;
Carmona, Guillaume ;
Iwasaki, Masayoshi ;
Mione, Marina ;
Koyanagi, Masamichi ;
Fischer, Ariane ;
Burchfield, Jana ;
Fox, Henrik ;
Doebele, Carmen ;
Ohtani, Kisho ;
Chavakis, Emmanouil ;
Potente, Michael ;
Tjwa, Marc ;
Urbich, Carmen ;
Zeiher, Andreas M. ;
Dimmeler, Stefanie .
SCIENCE, 2009, 324 (5935) :1710-1713
[9]
MicroRNA-34a regulates cardiac ageing and function [J].
Boon, Reinier A. ;
Iekushi, Kazuma ;
Lechner, Stefanie ;
Seeger, Timon ;
Fischer, Ariane ;
Heydt, Susanne ;
Kaluza, David ;
Treguer, Karine ;
Carmona, Guillaume ;
Bonauer, Angelika ;
Horrevoets, Anton J. G. ;
Didier, Nathalie ;
Girmatsion, Zenawit ;
Biliczki, Peter ;
Ehrlich, Joachim R. ;
Katus, Hugo A. ;
Mueller, Oliver J. ;
Potente, Michael ;
Zeiher, Andreas M. ;
Hermeking, Heiko ;
Dimmeler, Stefanie .
NATURE, 2013, 495 (7439) :107-110
[10]
MicroRNA-29 in Aortic Dilation: Implications for Aneurysm Formation [J].
Boon, Reinier A. ;
Seeger, Timon ;
Heydt, Susanne ;
Fischer, Ariane ;
Hergenreider, Eduard ;
Horrevoets, Anton J. G. ;
Vinciguerra, Manlio ;
Rosenthal, Nadia ;
Sciacca, Sergio ;
Pilato, Michele ;
van Heijningen, Paula ;
Essers, Jeroen ;
Brandes, Ralf P. ;
Zeiher, Andreas M. ;
Dimmeler, Stefanie .
CIRCULATION RESEARCH, 2011, 109 (10) :1115-U66