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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:
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.
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页码:755 / 762
页数:8
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