Freeman H J, San R H
Cancer Res. 1980 Sep;40(9):3155-7.
Mucosal cells freshly isolated from human intestine with pronase retain the capacity to undergo DNA repair synthesis (unscheduled DNA synthesis) during a 2-hr exposure to the carcinogen, N-methyl-N'-nitro-N-nitrosoguanidine, and the procarcinogen, aflatoxin B1. This procedure combining the use of human intestinal mucosal cells and the measurement of unscheduled DNA synthesis may provide a highly relevant and convenient test system for the detection of cell-specific, direct-acting, and activation-dependent chemical carcinogens. The use of whole-cell preparations in such in vitro studies may be of additional significance in view of growing evidence for artefactual metabolism by subcellular fractions.
用链霉蛋白酶从人肠道新鲜分离的黏膜细胞,在接触致癌物N-甲基-N'-硝基-N-亚硝基胍和前致癌物黄曲霉毒素B1的2小时内,保留了进行DNA修复合成(非定 期DNA合成)的能力。这种将人肠道黏膜细胞的使用与非定 期DNA合成的测量相结合的方法,可能为检测细胞特异性、直接作用和激活依赖性化学致癌物提供一个高度相关且便捷的测试系统。鉴于越来越多的证据表明亚细胞组分存在人为代谢现象,在这类体外研究中使用全细胞制剂可能具有额外的意义。