Jang Yin-Jin, Cha Eun-Young, Kim Woo-Young, Park Seong Wook, Shon Ji-Hong, Lee Sang Seop, Shin Jae-Gook
Department of Pharmacology, Inje University College of Medicine, Gaegum-dong, Jin-gu, Busan, Korea.
Ther Drug Monit. 2007 Jun;29(3):292-8. doi: 10.1097/FTD.0b013e318058a4e0.
Cytochrome P450 2S1 (CYP2S1) is a drug-metabolizing enzyme that shows interindividual variations in response to treatments for psoriasis and is regarded as a putative prognostic marker for colorectal cancer treatment. To gain insight into the genetic basis for the interindividual variations, CYP2S1 gene polymorphisms were analyzed in Korean subjects. Using direct sequencing of the CYP2S1 gene, 12 genetic variations, which included the two novel nonsynonymous mutations CYP2S1 S61N (0.3%) and CYP2S1 L230R (0.8%), were identified in 50 Korean subjects. Homology modeling predicted the location of the L230R change to be near two conserved alpha-helices in the hood of the substrate-binding site. Linkage disequilibrium (LD) analysis with seven common CYP2S1 variations showed two discrete LD blocks in CYP2S1 gene and consequently a limited number of haplotypes. Although the importance of novel CYP2S1 variants and haplotypes remains to be discovered, CYP2S1 polymorphisms would provide useful information on interindividual variations with respect to CYP2S1 function, which facilitates drug response predictions and disease prognosis.
细胞色素P450 2S1(CYP2S1)是一种药物代谢酶,在银屑病治疗反应中表现出个体差异,被认为是结直肠癌治疗的一种潜在预后标志物。为了深入了解个体差异的遗传基础,对韩国受试者的CYP2S1基因多态性进行了分析。通过对CYP2S1基因进行直接测序,在50名韩国受试者中鉴定出12种基因变异,其中包括两种新的非同义突变CYP2S1 S61N(0.3%)和CYP2S1 L230R(0.8%)。同源性建模预测L230R变化的位置靠近底物结合位点帽区的两个保守α螺旋。对7种常见的CYP2S1变异进行连锁不平衡(LD)分析,结果显示CYP2S1基因存在两个离散的LD块,因此单倍型数量有限。尽管新型CYP2S1变异和单倍型的重要性仍有待发现,但CYP2S1多态性将为CYP2S1功能的个体差异提供有用信息,这有助于药物反应预测和疾病预后评估。