Cholesteryl ester transfer protein and its inhibitors

被引:67
|
作者
Shrestha, Sudichhya [1 ]
Wu, Ben J. [1 ]
Guiney, Liam [2 ]
Barter, Philip J. [1 ]
Rye, Kerry-Anne [1 ]
机构
[1] Univ New South Wales Sydney, Sch Med Sci, Sydney, NSW, Australia
[2] Prince Wales Hosp, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
lipid transfers; atherosclerosis; lipoproteins; HIGH-DENSITY-LIPOPROTEIN; APOLIPOPROTEIN-A-I; BACTERICIDAL/PERMEABILITY-INCREASING PROTEIN; NEUTRALIZING MONOCLONAL-ANTIBODY; MODERATE ALCOHOL-CONSUMPTION; CORONARY-HEART-DISEASE; CETP-TRANSGENIC MICE; STEROL UP-REGULATION; MESSENGER-RNA LEVELS; HDL-CHOLESTEROL;
D O I
10.1194/jlr.R082735
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
Most of the cholesterol in plasma is in an esterified form that is generated in potentially cardioprotective HDLs. Cholesteryl ester transfer protein (CETP) mediates bidirectional transfers of cholesteryl esters (CEs) and triglycerides (TGs) between plasma lipoproteins. Because CE originates in HDLs and TG enters the plasma as a component of VLDLs, activity of CETP results in a net mass transfer of CE from HDLs to VLDLs and LDLs, and of TG from VLDLs to LDLs and HDLs. As inhibition of CETP activity increases the concentration of HDL-cholesterol and decreases the concentration of VLDL- and LDL-cholesterol, it has the potential to reduce atherosclerotic CVD. This has led to the development of anti-CETP neutralizing monoclonal antibodies, vaccines, and antisense oligonucleotides. Small molecule inhibitors of CETP have also been developed and four of them have been studied in large scale cardiovascular clinical outcome trials. This review describes the structure of CETP and its mechanism of action. Details of its regulation and nonlipid transporting functions are discussed, and the results of the large scale clinical outcome trials of small molecule CETP inhibitors are summarized.
引用
收藏
页码:772 / 783
页数:12
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