Nesnow S, Garland H, Curtis G
Carcinogenesis. 1982;3(4):377-80. doi: 10.1093/carcin/3.4.377.
Oncogenic transformation of C3H10T1/2CL8 cells was improved by treating the cells 5 days after seeding. Benzo[a]-pyrene-induced transformation was increased 3.5-fold by this method, compared with treating the cells 1 day after seeding. N-Methyl-N'-nitro-N-nitrosoguanidine, which does not transform asynchronous cultures of C3H10T1/2CL8 cells when administered 1 day after seeding, produced on average of 1 focus/dish, with 61% of the dishes exhibiting foci, when administered 5 days after seeding. Propane sultone and aflatoxin B1 also produced marked transformation responses when administered 5 days after seeding. However, 4-dimethylaminoazobenzene did not induce transformation when administered either 1 day or 5 days after seeding. With all chemicals examined, clonal cytotoxicity was reduced when they were administered 5 days after seeding. These results indicate the utility of this new procedure for the qualitative analysis of the transforming ability of chemicals.
在接种后5天处理C3H10T1/2CL8细胞可提高其致癌转化能力。与接种后1天处理细胞相比,用这种方法苯并[a]芘诱导的转化增加了3.5倍。接种后1天给予N-甲基-N'-硝基-N-亚硝基胍不能使C3H10T1/2CL8细胞的异步培养物发生转化,而接种后5天给予该物质平均每平皿产生1个集落,61%的平皿出现集落。接种后5天给予丙烷磺内酯和黄曲霉毒素B1也产生了明显的转化反应。然而,接种后1天或5天给予4-二甲基氨基偶氮苯均未诱导转化。对于所有检测的化学物质,接种后5天给予时克隆细胞毒性降低。这些结果表明了这种新方法在化学物质转化能力定性分析中的实用性。