Hemminki K, Försti A, Mustonen R, Savela K
J Cancer Res Clin Oncol. 1986;112(3):181-8. doi: 10.1007/BF00395910.
The role of DNA adducts in the initiation of cancer is scrutinized in this presentation. Work on the activation of oncogenes, particularly on ras, has provided new evidence to link DNA adducts and tumour formation. Polycyclic hydrocarbons and nitroso compounds can cause activation of ras oncogenes through a defined point mutation. The properties of two DNA binding agents, styrene oxide and cisplatin are discussed. Styrene oxide is a versatile electrophile causing numerous adducts; cisplatin has a high specificity towards guanine-N-7 and cross-link formation. Finally, the relation of specific adducts to carcinogenic potency as defined by TD50 values is investigated. For small alkyl groups, O-alkylation of bases correlates with potency but among others, particularly the bulky carcinogens, 7-alkylguanines appear as correlates of potency. Most such potent agents forming 7-alkylguanines induce depurination and imidazole ring-opening.
本报告详细探讨了DNA加合物在癌症起始过程中的作用。关于癌基因激活的研究,特别是对ras基因的研究,为DNA加合物与肿瘤形成之间的联系提供了新证据。多环烃和亚硝基化合物可通过特定的点突变导致ras癌基因激活。文中讨论了两种DNA结合剂——氧化苯乙烯和顺铂的特性。氧化苯乙烯是一种多用途亲电试剂,能产生多种加合物;顺铂对鸟嘌呤-N-7具有高度特异性并能形成交联。最后,研究了特定加合物与由TD50值定义的致癌效力之间的关系。对于小烷基,碱基的O-烷基化与效力相关,但在其他物质中,尤其是体积较大的致癌物,7-烷基鸟嘌呤似乎与效力相关。大多数形成7-烷基鸟嘌呤的强效试剂会诱导脱嘌呤和咪唑环开环。