Guengerich F P, Shimada T
Department of Biochemistry and Center in Molecular Toxicology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Mutat Res. 1998 May 25;400(1-2):201-13. doi: 10.1016/s0027-5107(98)00037-2.
Enzymatic transformation of most chemical carcinogens is requisite to the formation of electrophiles that cause genotoxicity, and the cytochrome P450 (P450) enzymes are the most prominent enzymes involved in such activation reactions. During the past 15 years the human P450 enzymes have been extensively characterized. Considerable evidence exists that the variation in activity of these enzymes can have important consequences in the actions of drugs. Other studies have been concerned with the activation of procarcinogens by human P450s. Assignments of roles of particular P450s in the metabolism of chemical carcinogens are discussed, along with the current state of evidence for relationships of particular P450s with human cancer.
大多数化学致癌物的酶促转化是形成具有基因毒性的亲电试剂所必需的,而细胞色素P450(P450)酶是参与此类激活反应的最主要酶类。在过去15年里,人类P450酶已得到广泛表征。有大量证据表明,这些酶活性的变化可能对药物作用产生重要影响。其他研究关注的是人类P450对前致癌物的激活作用。本文讨论了特定P450在化学致癌物代谢中的作用,以及特定P450与人类癌症关系的现有证据状况。