Therapeutic potential of antisense oligonucleotides for the management of dyslipidemia

被引:7
作者
Crooke, Rosanne M. [1 ]
Graham, Mark J. [1 ]
机构
[1] Isis Pharmaceut, Cardiovasc Res Antisense Drug Discovery, Carlsbad, CA 92010 USA
关键词
2'MOE gapmer; antisense oligonucleotides; ApoB-100; ApoC-III; CETP; dyslipidemia; Lp(a); mipomersen; miRNAs; APOLIPOPROTEIN-C-III; ESTER TRANSFER PROTEIN; DENSITY-LIPOPROTEIN CHOLESTEROL; INDUCED HEPATIC STEATOSIS; CORONARY-ARTERY-DISEASE; B SYNTHESIS INHIBITION; ADD-ON THERAPY; CARDIOVASCULAR-DISEASE; INSULIN-RESISTANCE; LDL-CHOLESTEROL;
D O I
10.2217/CLP.11.59
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Despite the availability of statins and other lipid-lowering drugs, cardiovascular disease is a leading cause of death in the USA and all industrialized nations, highlighting the need for additional therapeutic modalities. Antisense oligonucleotides, which are designed to alter the metabolism of RNA, are a new class of therapeutic agents that shows great promise for the treatment of dyslipidemias. A key advantage of the technology is the ability to selectively inhibit targets that cannot be modulated by traditional therapeutics such as structural proteins, transcription factors, lipoproteins, miRNAs and emerging factors that may influence lipid and lipoprotein metabolism. This review will describe the antisense technology platform, highlight preclinical data of antisense oligonucleotides targeting several risk factors that contribute to dyslipidemia and finally summarize the preclinical and clinical results relating to mipomersen, the most advanced cardiovascular antisense therapeutic agent, a second-generation 2' methoxyethyl gapmer inhibitor of human ApoB-100.
引用
收藏
页码:675 / 692
页数:18
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