Robichová S, Slamenová D
Department of Mutagenesis and Carcinogenesis, Cancer Research Institute, Slovak Academy of Sciences, 833 91 Bratislava, Slovak Republic.
Nutr Cancer. 2001;39(2):267-72. doi: 10.1207/S15327914nc392_17.
We have studied the genotoxic effects of the well-known heterocyclic liver carcinogen N-nitrosomorpholine (NMOR), an N-nitroso compound, which was prepared in our laboratory by nitrosation of the secondary amine morpholine with NaNO2. NMOR induced DNA strand breaks in human colon carcinoma Caco-2 cells. The concentration-dependent DNA-damaging effects of NMOR were proved by the comet assay. We further characterized DNA strand breaks induced by NMOR as follows: 1) We pretreated cells with vitamins E and C, which are able to eliminate oxidative DNA damage. 2) We varied the pH of the comet assay (12.1 and 13). In general, alkali-labile sites are stable until pH is raised to 12.5. 3) We used the site-specific repair enzymes exonuclease III and formamidopyrimidine-DNA glycosylase in the modified comet assay. Results showed that NMOR-induced DNA strand breaks have their origin exclusively in alkali-labile sites. Nevertheless, vitamins E and C decreased the level of DNA strand breaks. These results showed that antioxidants may have biological activities other than free radical scavenging that relate to their cancer-prevention properties. Our conceptions about reduction of NMOR-induced DNA lesions in Caco-2 cells by vitamins E and C are presented in this work.
我们研究了著名的杂环类肝脏致癌物N-亚硝基吗啉(NMOR)的遗传毒性作用,NMOR是一种N-亚硝基化合物,由我们实验室通过用亚硝酸钠对仲胺吗啉进行亚硝化反应制备而成。NMOR可诱导人结肠癌细胞Caco-2中的DNA链断裂。彗星试验证明了NMOR浓度依赖性的DNA损伤作用。我们进一步对NMOR诱导的DNA链断裂进行了如下特征描述:1)我们用能够消除氧化性DNA损伤的维生素E和维生素C对细胞进行预处理。2)我们改变了彗星试验的pH值(12.1和13)。一般来说,碱不稳定位点在pH值升至12.5之前是稳定的。3)我们在改良的彗星试验中使用了位点特异性修复酶外切核酸酶III和甲酰胺嘧啶-DNA糖基化酶。结果表明,NMOR诱导的DNA链断裂完全源于碱不稳定位点。然而,维生素E和维生素C降低了DNA链断裂的水平。这些结果表明,抗氧化剂可能具有除自由基清除之外的其他生物活性,这些活性与其防癌特性有关。本文介绍了我们关于维生素E和维生素C减少Caco-2细胞中NMOR诱导的DNA损伤的观点。