Zwelling L A, Mattern M R
Mutat Res. 1982 May-Jun;104(4-5):295-304. doi: 10.1016/0165-7992(82)90159-2.
The ability of the DNA intercalator m-AMSA to produce protein-associated DNA-strand breaks in normal, xeroderma pigmentosum and ataxia-telangiectasia fibroblasts was compared with m-AMSA uptake and cytotoxicity. No differences were detected between the cytotoxicity and DNA breakage produced by this antineoplastic acridine derivative among these three human cell lines. Uptake studies confirmed that no actual increased sensitivity was being masked by decreased intracellular drug. m-AMSA appears to be unique in its ability to produce breaks in cellular DNA that are not associated with an enhanced sensitivity in repair-deficient cells. Intercalator-induced, protein-associated DNA breaks are probably the result of a novel cellular response which differs from that which is abnormal in xeroderma pigmentosum or ataxia-telangiectasia cells.
将DNA嵌入剂m-AMSA在正常、着色性干皮病和共济失调-毛细血管扩张症成纤维细胞中产生与蛋白质相关的DNA链断裂的能力,与m-AMSA摄取及细胞毒性进行了比较。在这三种人类细胞系中,未检测到这种抗肿瘤吖啶衍生物产生的细胞毒性和DNA断裂之间存在差异。摄取研究证实,细胞内药物减少并未掩盖实际增加的敏感性。m-AMSA在产生细胞DNA断裂方面的能力似乎是独特的,这些断裂与修复缺陷细胞中增强的敏感性无关。嵌入剂诱导的、与蛋白质相关的DNA断裂可能是一种新型细胞反应的结果,这种反应不同于着色性干皮病或共济失调-毛细血管扩张症细胞中的异常反应。