miRNAs in atherosclerotic plaque initiation, progression, and rupture

被引:171
作者
Andreou, Loannis [1 ,2 ]
Sun, Xinghui [1 ]
Stone, Peter H. [1 ]
Edelman, Elazer R. [1 ,2 ]
Feinberg, Mark W. [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Cardiovasc, Boston, MA 02115 USA
[2] MIT, Inst Med Engn & Sci, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
atherosclerosis; miRNAs; inflammation; shear stress; vulnerable plaque; HIGH-DENSITY-LIPOPROTEIN; SMOOTH-MUSCLE-CELLS; REVERSE CHOLESTEROL TRANSPORT; INFLAMMATORY RESPONSE; MACROPHAGE ACTIVATION; ENDOTHELIAL-CELLS; PHENOTYPIC SWITCH; NUCLEAR RECEPTOR; LIPID-METABOLISM; GENE-REGULATION;
D O I
10.1016/j.molmed.2015.02.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Atherosclerosis is a chronic immune-inflammatory disorder that integrates multiple cell types and a diverse set of inflammatory mediators. miRNAs are emerging as important post-transcriptional regulators of gene expression in most, if not all, vertebrate cells, and constitute central players in many physiological and pathological processes. Rapidly accumulating experimental studies reveal their key role in cellular and molecular processes related to the development of atherosclerosis. We review current evidence for the involvement of miRNAs in early atherosclerotic lesion formation and in plaque rupture and erosion. We conclude with a perspective on the clinical relevance, therapeutic opportunities, and future challenges of miRNA biology in understanding the pathogenesis of this complex disease.
引用
收藏
页码:307 / 318
页数:12
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