Miller E C, Miller J A
Cancer. 1981 May 15;47(10):2327-45. doi: 10.1002/1097-0142(19810515)47:10<2327::aid-cncr2820471003>3.0.co;2-z.
Studies on a variety of chemical carcinogens have demonstrated that their ultimate reactive and carcinogenic forms are strong electrophiles. Some carcinogens, such as alkylating agents, are in their ultimate forms as administered, but most require metabolism to these active derivatives. The ultimate carcinogens react, usually non-enzymatically, with nucleophilic constituents in vivo. Of particular interest in regard to their possible importance in carcinogenesis have been the covalent interactions of these electrophilic reactants with cellular informational macromolecules, the DNAs, RNAs, and proteins. Current data are consistent with the idea that the initiation step of chemical carcinogenesis is a mutagenic event and is caused by alteration of DNA by the ultimate carcinogens. The nature of the carcinogen metabolite(s) involved in the promotion phase has not been determined, but there appears to be no requirement that they be electrophilic. The development of the concept of ultimate chemical carcinogens as strong electrophilic reactants is reviewed, especially with respect to the studies carried in the authors' laboratory.
对多种化学致癌物的研究表明,它们最终的反应性和致癌形式是强亲电试剂。一些致癌物,如烷基化剂,给药时即处于最终形式,但大多数需要代谢成这些活性衍生物。最终致癌物通常在体内以非酶促方式与亲核成分发生反应。就其在致癌过程中可能的重要性而言,特别令人感兴趣的是这些亲电反应物与细胞信息大分子(DNA、RNA和蛋白质)的共价相互作用。目前的数据与化学致癌起始步骤是致突变事件且由最终致癌物改变DNA所引起这一观点一致。促进阶段所涉及的致癌物代谢物的性质尚未确定,但似乎并不要求它们是亲电试剂。本文综述了将最终化学致癌物视为强亲电反应物这一概念的发展,尤其涉及作者实验室所开展的研究。