Dolan M E, Corsico C D, Pegg A E
Biochem Biophys Res Commun. 1985 Oct 15;132(1):178-85. doi: 10.1016/0006-291x(85)91004-6.
Exposure of HeLa S3 cells to 0.4mM 0(6)-methylguanine or 0(6)-n-butylguanine for 24 h led to a substantial decrease in the activity of 0(6)-alkylguanine-DNA alkyltransferase. Such pretreatment caused a marked increase in the sensitivity of the cells to the cytotoxic effects of the cross-linking alkylating agent 1-(2-chloroethyl)-1-nitroso-3-cyclohexylurea and a smaller increase in the sensitivity to N-methyl-N'-nitro-N-nitrosoguanidine. These results indicate that the repair of DNA by the alkyltransferase plays an important role in the protection of cells from the cytotoxic effects of certain alkylating agents particularly those such as 1-(2-chloroethyl)-1-nitroso-3-cyclohexylurea which ultimately lead to the formation of lethal interstrand cross-links.
将HeLa S3细胞暴露于0.4mM的O(6)-甲基鸟嘌呤或O(6)-正丁基鸟嘌呤24小时,导致O(6)-烷基鸟嘌呤-DNA烷基转移酶的活性大幅下降。这种预处理使细胞对交联烷化剂1-(2-氯乙基)-1-亚硝基-3-环己基脲的细胞毒性作用的敏感性显著增加,而对N-甲基-N'-硝基-N-亚硝基胍的敏感性增加较小。这些结果表明,烷基转移酶对DNA的修复在保护细胞免受某些烷化剂的细胞毒性作用中起着重要作用,尤其是那些最终导致形成致命链间交联的烷化剂,如1-(2-氯乙基)-1-亚硝基-3-环己基脲。