MicroRNA therapeutics for cardiovascular disease: opportunities and obstacles

被引:518
作者
van Rooij, Eva [2 ]
Olson, Eric N. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[2] MiRagen Therapeut, Boulder, CO 80301 USA
关键词
IN-VIVO; COLLAGEN EXPRESSION; CARDIAC-HYPERTROPHY; GENE-EXPRESSION; RENAL FIBROSIS; MESSENGER-RNAS; UP-REGULATION; HUMAN HEART; CELL; INHIBITION;
D O I
10.1038/nrd3864
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In recent years, prominent roles for microRNAs (miRNAs) have been uncovered in several cardiovascular disorders. The ability to therapeutically manipulate miRNA expression and function through systemic or local delivery of miRNA inhibitors, referred to as antimiRs, has triggered enthusiasm for miRNAs as novel therapeutic targets. Here, we focus on the pharmacokinetic and pharmacodynamic properties of current antimiR designs and their relevance to cardiovascular indications, and evaluate the opportunities and obstacles associated with this new therapeutic modality.
引用
收藏
页码:860 / 872
页数:13
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