School of Medical Sciences, University of New South Wales Sydney, Sydney, New South Wales, Australia.
Prince of Wales Hospital, Sydney, New South Wales, Australia.
J Lipid Res. 2018 May;59(5):772-783. doi: 10.1194/jlr.R082735. Epub 2018 Feb 27.
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.
血浆中的大部分胆固醇以酯化形式存在,这种酯化形式存在于具有潜在心脏保护作用的高密度脂蛋白(HDL)中。胆固醇酯转移蛋白(CETP)介导胆固醇酯(CE)和甘油三酯(TG)在血浆脂蛋白之间的双向转移。由于 CE 来源于 HDL,而 TG 作为 VLDL 的组成部分进入血浆,因此 CETP 的活性导致 CE 从 HDL 向 VLDL 和 LDL 的净质量转移,以及 TG 从 VLDL 向 LDL 和 HDL 的净质量转移。由于抑制 CETP 活性可增加 HDL-胆固醇的浓度并降低 VLDL-和 LDL-胆固醇的浓度,因此它有可能降低动脉粥样硬化性心血管疾病(CVD)的风险。这导致了抗 CETP 中和单克隆抗体、疫苗和反义寡核苷酸的开发。CETP 的小分子抑制剂也已被开发出来,其中有 4 种已在大规模心血管临床结局试验中进行了研究。本文描述了 CETP 的结构及其作用机制。详细讨论了其调节和非脂质转运功能,并总结了小分子 CETP 抑制剂的大规模临床结局试验结果。