Roos I A, Wakelin L P, Henry S J
Biochem J. 1985 Feb 15;226(1):175-82. doi: 10.1042/bj2260175.
The intracellular DNA damage produced by a series of diacridines after a 2 h pulse treatment of L1210 cells in culture was investigated by using the alkaline-elution technique. Like other intercalating agents, diacridines produce single-strand breaks and protein-DNA links. There is a large increase in both types of damage as the alkane chain linking the two 9-aminoacridine residues is increased beyond five methylene groups, which is consistent with the previously observed change from monofunctional to bifunctional intercalation [Wakelin, Romanos, Chen, Glaubiger, Canellakis & Waring (1978) Biochemistry 17, 5057-5063]. For linker chains of less than six methylene groups these agents produce less DNA damage than does the parent 9-aminoacridine at the same drug concentration. Unlike the monofunctional intercalators previously investigated [Ross, Glaubiger & Kohn (1979) Biochim. Biophys. Acta 562, 41-50; Zwelling, Michaels, Erickson, Ungerleider, Nichols & Kohn (1981) Biochemistry 20, 6553-6563; Zwelling, Kerrigan & Michaels (1982) Cancer Res. 42, 2687-2691; Zwelling, Michaels, Kerrigan, Pommier & Kohn (1982) Biochem. Pharmacol. 31, 3261-3267], there is no correlation between the number of single-strand breaks and protein-DNA links produced by these diacridines.
运用碱性洗脱技术,研究了一系列二吖啶在体外对L1210细胞进行2小时脉冲处理后所产生的细胞内DNA损伤。与其他嵌入剂一样,二吖啶会产生单链断裂和蛋白质-DNA连接。当连接两个9-氨基吖啶残基的烷烃链长度增加到超过五个亚甲基时,这两种损伤类型均大幅增加,这与之前观察到的从单功能嵌入到双功能嵌入的转变是一致的[瓦克林、罗曼诺斯、陈、格劳比格、卡内拉基斯和韦林(1978年)《生物化学》17卷,5057 - 5063页]。对于亚甲基少于六个的连接链,在相同药物浓度下,这些试剂所产生的DNA损伤比母体9-氨基吖啶要少。与之前研究的单功能嵌入剂不同[罗斯、格劳比格和科恩(1979年)《生物化学与生物物理学报》562卷,41 - 50页;兹韦林、迈克尔斯、埃里克森、昂格尔莱德、尼科尔斯和科恩(1981年)《生物化学》20卷,6553 - 6563页;兹韦林、克里根和迈克尔斯(1982年)《癌症研究》42卷,2687 - 2691页;兹韦林、迈克尔斯、克里根、波米耶尔和科恩(1982年)《生化药理学》31卷,3261 - 3267页],这些二吖啶产生的单链断裂数量与蛋白质-DNA连接数量之间没有相关性。