Children's Hospital Oakland Research Institute, CA 94609, USA.
Trends Cardiovasc Med. 2009 Jul;19(5):173-7. doi: 10.1016/j.tcm.2009.10.003.
Statins, or 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR) inhibitors, are widely prescribed to lower plasma cholesterol levels and reduce cardiovascular disease risk. Despite the well-documented efficacy of statins, there is large interindividual variation in response. Using a panel of immortalized lymphocyte cell lines incubated with simvastatin, we recently found that the magnitude of expression of an alternatively spliced HMGCR transcript lacking exon 13 was inversely correlated with in vivo reductions of total cholesterol, low-density lipoprotein cholesterol, apoB, and triglycerides after statin treatment of the individuals from whom the cells were derived. This review will discuss the potential significance of alternative splicing as a mechanism contributing to variation in statin efficacy as well as the use of immortalized lymphocyte cell lines for identifying pharmacogenetically relevant polymorphisms and molecular mechanisms.
他汀类药物,或 3-羟基-3-甲基戊二酰辅酶 A 还原酶(HMGCR)抑制剂,被广泛用于降低血浆胆固醇水平和降低心血管疾病风险。尽管他汀类药物的疗效已有充分的记录,但个体间的反应存在很大差异。我们最近使用经过辛伐他汀孵育的永生淋巴细胞细胞系进行研究,发现缺失外显子 13 的 HMGCR 转录本的表达幅度与个体接受他汀类药物治疗后总胆固醇、低密度脂蛋白胆固醇、载脂蛋白 B 和甘油三酯的体内降低程度呈负相关,这些个体来自于细胞的来源。这篇综述将讨论作为导致他汀类药物疗效个体差异的机制之一的选择性剪接的潜在意义,以及永生淋巴细胞细胞系在鉴定与药物遗传学相关的多态性和分子机制方面的应用。