Long Noncoding RNAs in Atherosclerosis and Vascular Injury Pathobiology, Biomarkers, and Targets for Therapy

被引:43
|
作者
Pierce, Jacob B. [1 ,2 ]
Feinberg, Mark W. [1 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Cardiovasc Div, Dept Med, Louis Pasteur Ave 77, Boston, MA 02115 USA
[2] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
atherosclerosis; biomarkers; cardiovascular diseases; oligonucleotides; percutaneous coronary intervention; SMOOTH-MUSCLE-CELLS; CHOLESTEROL HOMEOSTASIS; CARDIOVASCULAR-DISEASE; LNCRNA MIAT; GENE; RISK; EXPRESSION; H19; IDENTIFICATION; POLYMORPHISMS;
D O I
10.1161/ATVBAHA.120.314222
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite major advances in the primary and secondary prevention of atherosclerosis and its risk factors, atherosclerotic cardiovascular disease remains a major clinical and financial burden on individuals and health systems worldwide. In addition, neointima formation and proliferation due to mechanical trauma to the vessel wall during percutaneous coronary interventions can lead to vascular restenosis and limit the longevity and effectiveness of coronary revascularization. Long noncoding RNAs (lncRNAs) have emerged as a novel class of epigenetic regulators with critical roles in the pathogenesis of atherosclerosis and restenosis following vascular injury. Here, we provide an in-depth review of lncRNAs that regulate the development of atherosclerosis or contribute to the pathogenesis of restenosis following mechanical vascular injury. We describe the diverse array of intracellular mechanisms by which lncRNAs exert their regulatory effects. We highlight the utility and challenges of lncRNAs as biomarkers. Finally, we discuss the immense translational potential of lncRNAs and strategies for targeting them therapeutically using oligonucleotide-based therapeutics and novel gene therapy platforms.
引用
收藏
页码:2002 / 2017
页数:16
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