Nanomedicine Meets microRNA: Current Advances in RNA-Based Nanotherapies for Atherosclerosis

被引:29
作者
Gadde, Suresh [1 ]
Rayner, Katey J. [1 ,2 ]
机构
[1] Univ Ottawa, Fac Med, Dept Biochem Microbiol & Immunol, Ottawa, ON K1N 6N5, Canada
[2] Univ Ottawa, Inst Heart, Ottawa, ON K1N 6N5, Canada
基金
美国国家卫生研究院;
关键词
drug delivery system; microRNA; microRNA stability; nanoparticle; nanotechnology; FATTY-ACID OXIDATION; SMOOTH-MUSCLE-CELLS; CHOLESTEROL HOMEOSTASIS; IN-VIVO; POLYMERIC NANOPARTICLES; NONHUMAN-PRIMATES; DRUG-DELIVERY; MIR-33; MICE; INFLAMMATION;
D O I
10.1161/ATVBAHA.116.307481
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiovascular disease (CVD) accounts for almost half of all deaths worldwide and has now surpassed infectious disease as the leading cause of death and disability in developing countries. At present, therapies such as low-density lipoprotein-lowering statins and antihypertensive drugs have begun to bend the morality curve for coronary artery disease (CAD); yet, as we come to appreciate the more complex pathophysiological processes in the vessel wall, there is an opportunity to fine-tune therapies to more directly target mechanisms that drive CAD. MicroRNAs (miRNAs) have been identified that control vascular cell homeostasis,(1-3) lipoprotein metabolism,(4-9) and inflammatory cell function.(10) Despite the importance of these miRNAs in driving atherosclerosis and vascular dysfunction, therapeutic modulation of miRNAs in a cell- and context-specific manner has been a challenge. In this review, we summarize the emergence of miRNA-based therapies as an approach to treat CAD by specifically targeting the pathways leading to the disease. We focus on the latest development of nanoparticles (NPs) as a means to specifically target the vessel wall and what the future of these nanomedicines may hold for the treatment of CAD.
引用
收藏
页码:e73 / e79
页数:7
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