Angiopoietin-Like 3 From Discovery to Therapeutic Gene Editing

被引:34
|
作者
Wang, Xiao [1 ,2 ]
Musunuru, Kiran [1 ,2 ]
机构
[1] Univ Penn, Perelman Sch Med, Cardiovasc Inst, Dept Med, 3400 Civ Ctr Blvd,Bldg 421,11-104 Smilow Ctr, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Cardiovasc Inst, Dept Genet, 3400 Civ Ctr Blvd,Bldg 421,11-104 Smilow Ctr, Philadelphia, PA 19104 USA
来源
JACC-BASIC TO TRANSLATIONAL SCIENCE | 2019年 / 4卷 / 06期
关键词
coronary artery disease; genetics; lipids; INNATE IMMUNE-RESPONSE; LIPID CONCENTRATIONS; LIPOPROTEIN-LIPASE; REDUCING LIPIDS; ADIPOSE FACTOR; ANGPTL3; PROTEIN; METABOLISM; MUTATIONS; BASE;
D O I
10.1016/j.jacbts.2019.05.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hyperlipidemia is a major causal risk factor for atherosclerosis and coronary heart disease (CHD). Angiopoietin-like 3 (ANGPTL3) has emerged as a promising molecular target to reduce CHD risk due to its regulation of all 3 major lipid traits: tow-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and triglycerides. Here, the authors review the discovery of ANGPTL3, the role of ANGPTL3 in lipoprotein metabolism, and the genetic association between naturally occurring ANGPTL3 loss-of-function mutations and CHD. In light of the favorable consequences of ANGPTL3 deficiency, various therapeutic strategies to target ANGPTL3 are currently in development, including a monoclonal antibody, an antisense oligonucleotide, and gene editing. (C) 2019 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.
引用
收藏
页码:755 / 762
页数:8
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