Hai Qimin, Smith Jonathan D
Department of Cardiovascular & Metabolic Sciences, Cleveland Clinic, Cleveland, OH 44195, USA.
Metabolites. 2021 Aug 14;11(8):543. doi: 10.3390/metabo11080543.
The purification and cloning of the acyl-coenzyme A: cholesterol acyltransferase (ACAT) enzymes and the sterol O-acyltransferase () genes has opened new areas of interest in cholesterol metabolism given their profound effects on foam cell biology and intestinal lipid absorption. The generation of mouse models deficient in or confirmed the importance of their gene products on cholesterol esterification and lipoprotein physiology. Although these studies supported clinical trials which used non-selective ACAT inhibitors, these trials did not report benefits, and one showed an increased risk. Early genetic studies have implicated common variants in both genes with human traits, including lipoprotein levels, coronary artery disease, and Alzheimer's disease; however, modern genome-wide association studies have not replicated these associations. In contrast, the common variants are most reproducibly associated with testosterone levels.
酰基辅酶A:胆固醇酰基转移酶(ACAT)和固醇O-酰基转移酶()基因的纯化与克隆,鉴于它们对泡沫细胞生物学和肠道脂质吸收具有深远影响,为胆固醇代谢研究开辟了新的关注领域。缺乏或的小鼠模型的产生证实了其基因产物在胆固醇酯化和脂蛋白生理学中的重要性。尽管这些研究为使用非选择性ACAT抑制剂的临床试验提供了支持,但这些试验并未报告有益结果,其中一项试验显示风险增加。早期的遗传学研究表明这两个基因中的常见变异与人类特征有关,包括脂蛋白水平、冠状动脉疾病和阿尔茨海默病;然而,现代全基因组关联研究并未重复这些关联。相比之下,常见的变异与睾酮水平的关联最为一致。