The PCSK9 decade

被引:368
作者
Lambert, Gilles [2 ,3 ]
Sjouke, Barbara [1 ]
Choque, Benjamin [3 ]
Kastelein, John J. P. [1 ]
Hovingh, G. Kees [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Vasc Med, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Nantes, Lab Inserm U957, Fac Med, Nantes, France
[3] Heart Res Inst, Lipid Res Grp, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
antibodies; cholesterol; drug therapy; low density lipoprotein metabolism; lipoprotein receptors; proprotein convertase subtilisin/kexin type 9; SUBTILISIN/KEXIN TYPE 9; C-TERMINAL DOMAIN; AUTOSOMAL-DOMINANT HYPERCHOLESTEROLEMIA; DENSITY-LIPOPROTEIN CHOLESTEROL; PLASMA PROPROTEIN CONVERTASE; LDL RECEPTOR DEGRADATION; FAMILIAL HYPERCHOLESTEROLEMIA; SECRETED PCSK9; MONOCLONAL-ANTIBODY; SERUM LDL;
D O I
10.1194/jlr.R026658
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
PCSK9 proprotein convertase subtilisin/kexin type (PCSK9) is a crucial protein in LDL cholesterol (LDL-C) metabolism by virtue of its pivotal role in the degradation of the LDL receptor. In recent years, both in vitro and in vivo studies have greatly supplemented our understanding of the (patho) physiological role of PCSK9 in human biology. In the current review, we summarize studies published or in print before May 2012 concerning the physiological role of PCSK9 in cholesterol metabolism. Moreover, we briefly describe the clinical phenotypes encountered in carriers of mutations in the gene encoding PCSK9. As PCSK9 has emerged as a novel target for LDL-C lowering therapy, methods to inhibit PCSK9 will also be reviewed. Initial data from investigations of PCSK9 inhibition in humans are promising and indicate that PCSK9 inhibition may be a viable new therapeutic option for the treatment of dyslipidemia and associated cardiovascular diseases.-Lambert, G., B. Sjouke, B. Choque, J. J. P. Kastelein, and G. K. Hovingh. The PCSK9 decade. J. Lipid Res. 2012. 53: 2515-2524.
引用
收藏
页码:2515 / 2524
页数:10
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