Erickson L C, Bradley M O, Kohn K W
Cancer Res. 1978 Oct;38(10):3379-84.
The DNA of V-79 Chinese hamster cells was examined by alkaline elution following treatment of cultures with eight different nitrosoureas. Drug incubations were performed under consistent biological conditions of equal toxicity and equal mutation induction at the hypoxanthineguanine phosphoribosyltransferase locus. The goals of this study were to determine whether DNA damage could be detected in cells treated with biologically relevant doses of nitrosoureas and to determine whether the type and number of observed DNA lesions could be correlated with the cytotoxic and mutagenic effects of the drugs. All of the compounds tested produced, to some degree, lesions that were observed as DNA strand breaks upon exposure of the DNA to alkali. The levels of DNA strand breaks and/or alkali-labile lesions were comparable for all of the drugs at the equimutagenic doses. DNA cross-linking was observed at both the equitoxic and the equimutagenic concentrations of the haloethylnitrosoureas, but cross-linking was not observed with methylnitrosourea or streptozotocin. Methylnitrosourea and streptozotocin required approximately 40 times the drug concentration to produce toxicity equal to the haloethylnitrosoureas. These data suggest that the ability to cross-link DNA confers increased cytotoxicity to the haloethylnitrosoureas.
在用八种不同的亚硝基脲处理培养物后,通过碱性洗脱法检测了V - 79中国仓鼠细胞的DNA。药物孵育在次黄嘌呤 - 鸟嘌呤磷酸核糖基转移酶位点具有相同毒性和相同诱变诱导的一致生物学条件下进行。本研究的目的是确定在用生物学相关剂量的亚硝基脲处理的细胞中是否能检测到DNA损伤,以及确定观察到的DNA损伤的类型和数量是否与药物的细胞毒性和诱变作用相关。所有测试的化合物在一定程度上都会产生损伤,当DNA暴露于碱中时,这些损伤表现为DNA链断裂。在等诱变剂量下,所有药物的DNA链断裂和/或碱不稳定损伤水平相当。在卤代乙基亚硝基脲的等毒性和等诱变浓度下均观察到DNA交联,但甲基亚硝基脲或链脲佐菌素未观察到交联。甲基亚硝基脲和链脲佐菌素产生与卤代乙基亚硝基脲相同毒性所需的药物浓度约为其40倍。这些数据表明,DNA交联能力赋予卤代乙基亚硝基脲更高的细胞毒性。