Thust R, Neupert G, Kleeberg U
Cancer Biochem Biophys. 1978;3(1):1-6.
Epithelial rat liver cell line RL-19 was checked for aryl hydrocarbon hydroxylase and dimethylnitrosamine demethylase activity. Aryl hydrocarbon hydroxylase activity was found at the rate of about 14.5 pmoles 3-hydroxy-benzopyrene per min per mg protein. This activity was not inducible by 3-methylcholanthrene or by phenobarbital and was independent of the subculture level. From the 45th up to the 59th subculture the mean demethylase activity was about 1.08 nmoles HCHO per min per mg protein, but was decreased to 0.64 nmoles HCHO per min per mg protein at the 131st subculture. RL-19 cells were treated with 3-methylcholanthrene (0.5-1.0 microgram/ml), dimethylnitrosamine (100-400 micrograms/ml), or Natulan (50 micrograms/ml), respectively, for 7 to 10 days. During a 6 months subsequent cultivation no neoplastic changes were observed as revealed by morphological investigation, soft agar assay, and transplantation. It is suggested that metabolic competence for carcinogen activation is only one prerequisite for neoplastic alteration in vitro, and that RL-19 cells are refractory to the action of carcinogens in spite of their metabolic capacity.
对大鼠肝上皮细胞系RL - 19进行了芳烃羟化酶和二甲基亚硝胺脱甲基酶活性检测。发现芳烃羟化酶活性约为每分钟每毫克蛋白质14.5皮摩尔3 - 羟基苯并芘。该活性不受3 - 甲基胆蒽或苯巴比妥诱导,且与传代水平无关。从第45代到第59代,平均脱甲基酶活性约为每分钟每毫克蛋白质1.08纳摩尔甲醛,但在第131代时降至每分钟每毫克蛋白质0.64纳摩尔甲醛。分别用3 - 甲基胆蒽(0.5 - 1.0微克/毫升)、二甲基亚硝胺(100 - 400微克/毫升)或纳图兰(50微克/毫升)处理RL - 19细胞7至10天。在随后6个月的培养过程中,通过形态学观察、软琼脂试验和移植均未观察到肿瘤性变化。提示致癌物激活的代谢能力只是体外肿瘤性改变的一个前提条件,并且RL - 19细胞尽管具有代谢能力,但对致癌物的作用具有抗性。