Williams G M
Cancer Lett. 1976 Mar;1(4):231-5. doi: 10.1016/s0304-3835(75)97171-2.
Primary rat liver cell cultures were exposed to a direct acting carcinogen, methyl methanesulfonate, and procarcinogens requiring metabolic activation, aflatoxin B1 and B2. DNA damage by these agents was evidenced by the induction of DNA repair, measured as unscheduled DNA synthesis. The sensitivity of these cultures to the potent porcarcinogen aflatoxin B1 indicates that this system may be adapted for screening suspected chemical procarcinogens, and for investigating the relationship between metabolic activation of procarcinogens, DNA damage, DNA repair, and carcinogenicity.
原代大鼠肝细胞培养物暴露于直接作用的致癌物甲磺酸甲酯以及需要代谢活化的前致癌物黄曲霉毒素B1和B2。这些试剂造成的DNA损伤通过DNA修复的诱导得以证明,DNA修复通过非预定DNA合成来衡量。这些培养物对强效前致癌物黄曲霉毒素B1的敏感性表明,该系统可用于筛选可疑的化学前致癌物,以及研究前致癌物的代谢活化、DNA损伤、DNA修复和致癌性之间的关系。