Proprotein convertase subtilisin/kexin type 9 inhibition

被引:35
作者
Marais, David A. [2 ]
Blom, Dirk J. [3 ]
Petrides, Francine [4 ]
Goueffic, Yann [5 ]
Lambert, Gilles [1 ,4 ]
机构
[1] Univ Nantes, Lab Inserm UMR957, Fac Med, F-44000 Nantes, France
[2] Univ Cape Town, Dept Chem Pathol, ZA-7925 Cape Town, South Africa
[3] Univ Cape Town, Dept Med, ZA-7925 Cape Town, South Africa
[4] Heart Res Inst, Lipid Res Grp, Sydney, NSW, Australia
[5] CHU Nantes, Inst Thorax, Serv Chirurg Vasc, F-44035 Nantes 01, France
基金
英国医学研究理事会;
关键词
cardiovascular disease; LDL receptor; monoclonal antibodies; proprotein convertase subtilisin/kexin type 9; DENSITY-LIPOPROTEIN RECEPTOR; C-TERMINAL DOMAIN; PLASMA LDL-CHOLESTEROL; FAMILIAL HYPERCHOLESTEROLEMIA; MONOCLONAL-ANTIBODY; NONHUMAN-PRIMATES; SECRETED PCSK9; MICE; DEGRADATION; BINDING;
D O I
10.1097/MOL.0b013e3283587563
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
Purpose of review There are now ample data that demonstrate that inhibition of PCSK9 (proprotein convertase subtilisin/kexin type 9) can safely lower LDL cholesterol synergistically with statins. Considering that PCSK9 was first identified less than a decade ago, the last few years have shown rapid and remarkable advancements in our understanding and knowledge of the structure and function of PCSK9. Recent findings Therapeutic developments have not lagged far behind with some monoclonal antibodies currently entering phase III trials. Of the many approaches to PCSK9 inhibition, these compounds are the furthest advanced in their clinical development while small molecule oral inhibitors seem a distant prospect. Summary This review summarizes the discovery and history of PCSK9 and in particular its mode of action as an inhibitor of the LDL receptor. It also recapitulates key studies that have demonstrated the potential of inhibiting PCSK9 to further decrease LDL-cholesterol levels safely and synergistically with statins. Finally, we review the strategies that are currently in development to inhibit PCSK9, with a special emphasis on the spectacular results from recent phase-I and phase-II clinical trials.
引用
收藏
页码:511 / 517
页数:7
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