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Polymorphisms of CYP2A6 and its practical consequences.

机译:CYP2A6的多态性及其实际结果。

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CYP2A6 is an hepatic enzyme predominantly with some expression in specialized extrahepatic cell types. The CYP2A6 enzyme has a somewhat restricted active site, accepting only a few xenobiotics as substrates. Interest in CYP2A6 has risen considerably after nicotine and some tobacco specific nitrosamines were established as high-affinity substrates for this enzyme. Recently, the organization and structures of the CYP2A gene cluster and several polymorphic alleles of the CYP2A6 gene have been characterized. Two alleles with a point mutation and at least three different types of gene deletion, all leading to deficient gene function, have been found. The frequencies of these alleles vary considerably among different ethnic populations, the deletion alleles being most common in Orientals (up to 20%). The frequency of point mutations are low in all populations studied thus far (< 3%). Several case-control studies have addressed the relationship between CYP2A6 status and smoking habits as well as the role of CYP2A6 polymorphism in lung cancer risk. Studies in Japanese suggest that CYP2A6 poor metabolizer genotypes result in altered nicotine kinetics and may lower cigarette smoking elicited lung cancer risk, whereas similar studies in Caucasian populations have not revealed any clear associations between variant CYP2A6 genotypes and smoking behaviour or lung cancer predisposition.
机译:CYP2A6是一种肝酶,主要在专门的肝外细胞类型中表达。 CYP2A6酶的活性位点有所限制,仅接受少量异种生物作为底物。尼古丁和一些烟草特有的亚硝胺被确立为该酶的高亲和力底物后,人们对CYP2A6的兴趣大大提高。最近,已经表征了CYP2A基因簇的组织和结构以及CYP2A6基因的几个多态性等位基因。已经发现了两个具有点突变和至少三种不同类型的基因缺失的等位基因,均导致基因功能不足。这些等位基因的频率在不同种族的人群中差异很大,缺失等位基因在东方人中最为常见(高达20%)。迄今为止,在所有研究的人群中,点突变的发生率都很低(<3%)。几项病例对照研究探讨了CYP2A6状况与吸烟习惯之间的关系,以及CYP2A6多态性在肺癌风险中的作用。日语研究表明,CYP2A6不良代谢者基因型会导致尼古丁动力学改变,并可能降低吸烟引发肺癌的风险,而在高加索人群中,类似的研究并未揭示CYP2A6变异基因型与吸烟行为或肺癌易感性之间的明确关联。

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