Department of Pharmacology, Penn State College of Medicine, 500 University Drive, CH69, Hershey, PA 17033, USA.
Drug Metab Dispos. 2010 Dec;38(12):2204-9. doi: 10.1124/dmd.110.035345. Epub 2010 Sep 1.
UDP-glucuronosyltransferases (UGTs) are enzymes involved in the metabolism of steroid hormones, carcinogens, cancer chemotherapy agents, and addictive agents from cigarettes. Because the UGT2B family of genes has been linked to hormonal regulation in human cell lines in vitro, we hypothesized that there may be sex-related differences in the expression and activity of these genes in human tissues. To evaluate whether there are sex differences in UGT2B expression and activity, we examined 103 normal human liver specimens for UGT2B expression by real-time polymerase chain reaction and in vitro glucuronidation activities in human liver microsomes (HLM). Men exhibited an approximately 4-fold higher level of expression of UGT2B17 than women (p = 0.007). Consistent with the increased expression of UGT2B17 in men, HLM from men also had a higher level of glucuronidation activity than HLM from women against three UGT2B17 substrates: 3-fold higher for 17-dihydroexemestane (p = 0.002); 3-fold higher for 3-hydroxycotinine (p < 0.001); and 1.5-fold higher for suberoylanilide hydroxamic acid (p = 0.014). When we stratified by UGT2B17 gene deletion genotype, similar patterns were observed for all three substrates, with HLM from men with the UGT2B17 (+/+) or (+/0) genotypes exhibiting significantly higher levels of glucuronidation activity against all three substrates compared with HLM from women. These data suggest that men have a higher amount of UGT2B17 glucuronidation activity then women. This sex difference in UGT2B17 gene expression and corresponding protein activity could potentially result in different levels of carcinogen detoxification or drug elimination in men versus women.
尿苷二磷酸葡萄糖醛酸转移酶(UGTs)参与甾体激素、致癌物、癌症化疗药物和香烟中成瘾物质的代谢。由于 UGT2B 家族的基因与体外人细胞系中的激素调节有关,我们假设这些基因在人组织中的表达和活性可能存在性别差异。为了评估 UGT2B 表达是否存在性别差异,我们通过实时聚合酶链反应和人肝微粒体(HLM)中的体外葡萄糖醛酸化活性检查了 103 个正常人类肝脏标本中的 UGT2B 表达。男性的 UGT2B17 表达水平比女性高约 4 倍(p = 0.007)。与男性 UGT2B17 表达增加一致,男性 HLM 对三种 UGT2B17 底物的葡萄糖醛酸化活性也高于女性 HLM:17-二氢表雄甾酮高 3 倍(p = 0.002);3-羟基可替宁高 3 倍(p < 0.001);和琥珀酰亚胺羟肟酸高 1.5 倍(p = 0.014)。当我们按 UGT2B17 基因缺失基因型分层时,所有三种底物都观察到类似的模式,与女性 HLM 相比,具有 UGT2B17 (+/+) 或 (+/0) 基因型的男性 HLM 对所有三种底物的葡萄糖醛酸化活性均显著升高。这些数据表明,男性的 UGT2B17 葡萄糖醛酸化活性高于女性。UGT2B17 基因表达和相应蛋白质活性的这种性别差异可能导致男性与女性在致癌物解毒或药物消除方面存在不同水平。