Ingelman-Sundberg Magnus
Division of Molecular Toxicology, IMM, Karolinska Institutet, SE-171 77 Stockholm, Sweden.
Toxicol Appl Pharmacol. 2005 Sep 1;207(2 Suppl):52-6. doi: 10.1016/j.taap.2005.01.030.
Currently, 57 active cytochrome P450 (CYP) genes and 58 pseudogenes are known to be present in the human genome. Among the genes discovered by initiatives in the human genome project are CYP2R1, CYP2W1, CYP2S1, CYP2U1 and CYP3A43, the latter apparently encoding a pseudoenzyme. The function, polymorphism and regulation of these genes are still to be discovered to a great extent. The polymorphism of drug metabolizing CYPs is extensive and influences the outcome of drug therapy causing lack of response or adverse drug reactions. The basis for the differences in the global distribution of the polymorphic variants is inactivating gene mutations and subsequent genetic drift. However, polymorphic alleles carrying multiple active gene copies also exist and are suggested in case of CYP2D6 to be caused by positive selection due to development of alkaloid resistance in North East Africa about 10,000-5000 BC. The knowledge about the CYP genes and their polymorphisms is of fundamental importance for effective drug therapy and for drug development as well as for understanding metabolic activation of carcinogens and other xenobiotics. Here, a short review of the current knowledge is given.
目前已知人类基因组中存在57个活性细胞色素P450(CYP)基因和58个假基因。人类基因组计划中发现的基因包括CYP2R1、CYP2W1、CYP2S1、CYP2U1和CYP3A43,后者显然编码一种假酶。这些基因的功能、多态性和调控在很大程度上仍有待发现。药物代谢CYP的多态性广泛,会影响药物治疗的结果,导致无反应或药物不良反应。多态性变体全球分布差异的基础是失活基因突变和随后的基因漂变。然而,携带多个活性基因拷贝的多态性等位基因也存在,对于CYP2D6而言,推测是由于公元前10000 - 5000年东北非地区生物碱抗性的发展导致正选择所致。关于CYP基因及其多态性的知识对于有效的药物治疗、药物开发以及理解致癌物和其他外源性物质的代谢活化至关重要。在此,对当前的知识进行简要综述。