Cholesteryl ester transfer protein (CETP) deficiency and CETP inhibitors
- PMID: 25410905
- PMCID: PMC4255097
- DOI: 10.14348/molcells.2014.0265
Cholesteryl ester transfer protein (CETP) deficiency and CETP inhibitors
Abstract
Epidemiologic studies have shown that low-density lipoprotein cholesterol (LDL-C) is a strong risk factor, whilst high-density lipoprotein cholesterol (HDL-C) reduces the risk of coronary heart disease (CHD). Therefore, strategies to manage dyslipidemia in an effort to prevent or treat CHD have primarily attempted at decreasing LDL-C and raising HDL-C levels. Cholesteryl ester transfer protein (CETP) mediates the exchange of cholesteryl ester for triglycerides between HDL and VLDL and LDL. We have published the first report indicating that a group of Japanese patients who were lacking CETP had extremely high HDL-C levels, low LDL-C levels and a low incidence of CHD. Animal studies, as well as clinical and epidemiologic evidences, have suggested that inhibition of CETP provides an effective strategy to raise HDL-C and reduce LDL-C levels. Four CETP inhibitors have substantially increased HDL-C levels in dyslipidemic patients. This review will discuss the current status and future prospects of CETP inhibitors in the treatment of CHD. At present anacetrapib by Merck and evacetrapib by Eli Lilly are under development. By 100mg of anacetrapib HDL-C increased by 138%, and LDL-C decreased by 40%. Evacetrapib 500 mg also showed dramatic 132% increase of HDL-C, while LDL-C decreased by 40%. If larger, long-term, randomized, clinical end point trials could corroborate other findings in reducing atherosclerosis, CETP inhibitors could have a significant impact in the management of dyslipidemic CHD patients. Inhibition of CETP synthesis by antisense oligonucleotide or small molecules will produce more similar conditions to human CETP deficiency and may be effective in reducing atherosclerosis and cardiovascular events. We are expecting the final data of prospective clinical trials by CETP inhibitors in 2015.
Keywords: CETP deficiency; HDL & LDL; cholesteryl ester transfer protein (CETP); hyper-HDL-cholesterolemia; inhibitors of CETP.
Figures




Similar articles
-
Future of cholesteryl ester transfer protein (CETP) inhibitors: a pharmacological perspective.Clin Pharmacokinet. 2013 Aug;52(8):615-26. doi: 10.1007/s40262-013-0071-8. Clin Pharmacokinet. 2013. PMID: 23658137 Free PMC article.
-
Re-evaluation of cholesteryl ester transfer protein function in atherosclerosis based upon genetics and pharmacological manipulation.Curr Opin Lipidol. 2016 Oct;27(5):459-72. doi: 10.1097/MOL.0000000000000332. Curr Opin Lipidol. 2016. PMID: 27454452 Review.
-
Cholesteryl ester transfer protein: An enigmatic pharmacology - Antagonists and agonists.Atherosclerosis. 2018 Nov;278:286-298. doi: 10.1016/j.atherosclerosis.2018.09.035. Epub 2018 Oct 1. Atherosclerosis. 2018. PMID: 30347344 Review.
-
Anacetrapib, but not evacetrapib, impairs endothelial function in CETP-transgenic mice in spite of marked HDL-C increase.Atherosclerosis. 2017 Feb;257:186-194. doi: 10.1016/j.atherosclerosis.2017.01.011. Epub 2017 Jan 16. Atherosclerosis. 2017. PMID: 28152406
-
On- and off-target pharmacology of torcetrapib: current understanding and implications for the structure activity relationships (SAR), discovery and development of cholesteryl ester-transfer protein (CETP) inhibitors.Drugs. 2012 Mar 5;72(4):491-507. doi: 10.2165/11599310-000000000-00000. Drugs. 2012. PMID: 22356288 Review.
Cited by
-
The Role of Triglyceride-rich Lipoproteins and Their Remnants in Atherosclerotic Cardiovascular Disease.Eur Cardiol. 2023 Sep 28;18:e56. doi: 10.15420/ecr.2023.16. eCollection 2023. Eur Cardiol. 2023. PMID: 37860700 Free PMC article. Review.
-
Dysfunctional High-Density Lipoprotein: An Innovative Target for Proteomics and Lipidomics.Cholesterol. 2015;2015:296417. doi: 10.1155/2015/296417. Epub 2015 Nov 8. Cholesterol. 2015. PMID: 26634153 Free PMC article. Review.
-
Translating atherosclerosis research from bench to bedside: navigating the barriers for effective preclinical drug discovery.Clin Sci (Lond). 2022 Dec 9;136(23):1731-1758. doi: 10.1042/CS20210862. Clin Sci (Lond). 2022. PMID: 36459456 Free PMC article.
-
Atherosclerosis: an overview of mouse models and a detailed methodology to quantify lesions in the aortic root.Vasc Biol. 2024 Apr 4;6(1):e230017. doi: 10.1530/VB-23-0017. Print 2024 Jan 1. Vasc Biol. 2024. PMID: 38428154 Free PMC article. Review.
-
A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration.Sci Rep. 2020 Jan 31;10(1):1584. doi: 10.1038/s41598-020-58510-9. Sci Rep. 2020. PMID: 32005911 Free PMC article.
References
-
- Agellon L.B., Walsh A., Hayek T., Moulin P., Jiang X.C., Shelanski S.A., Breslow J.L., Tall A.R. Reduced high-density lipoprotein cholesterol in human cholesteryl ester transfer protein transgenic mice. J. Biol. Chem. 1991;266:10796–10801. - PubMed
-
- Barter P.J., Brewer H.B., Jr., Chapman M.J., Hennekens C.H., Rader D.J., Tall A.R. Cholesteryl ester transfer protein: a novel target for raising HDL and inhibiting atherosclerosis. Arterioscler. Thromb. Vasc. Biol. 2003;23:160–167. - PubMed
-
- Brewer H.B., Jr. Increasing HDL cholesterol levels. N. Engl. J. Med. 2004;350:1491–1494. - PubMed
-
- Brousseau M.E., Schaefer E.J., Wolfe M.L., Bloedon L.T., Digenio A.G., Clark R.W., Mancuso J.P., Rader D.J. Effects of an inhibitor of cholesteryl ester transfer protein on HDL cholesterol. N. Engl. J. Med. 2004;350:1505–1515. - PubMed
Publication types
MeSH terms
Substances
Supplementary concepts
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical