Department of Toxicology, University of Hamburg Medical School, Martinistrasse 52, 2000 Hamburg 20, GFR.
Carcinogenesis. 1980 Mar;1(3):215-8. doi: 10.1093/carcin/1.3.215.
Malignant transformation and mutation to ouabain-resistance is induced in cloned M2 mouse fibroblasts in vitro by treatment with N-methyl-N'-nitro-N-nitrosoguanidine and two derivatives of polycyclic aromatic hydrocarbons, the 3,4-diol derived from 7-methylbenz [a]anthracene and the 7,8-diol-9,10-oxide derived from benzo[a]pyrene. Transformation is an event more frequent than mutation, the ratio of transformation to mutation frequencies varied between 24 and 1118. Another hydrocarbon derivative, the 9,10-diol-7,8-oxide derived from benzo[a]pyrene, did induce ouabain-resistance without causing transformation. Induced ouabain-resistant clones did not behave like transformants, and transformants did not exhibit ouabain resistance. The significance of these findings is discussed.
在体外,用 N-甲基-N'-硝基-N-亚硝基胍和两种多环芳烃衍生物(7-甲基苯并[a]蒽衍生的 3,4-二醇和苯并[a]芘衍生的 7,8-二醇-9,10-氧化物)处理克隆的 M2 小鼠成纤维细胞,可诱导恶性转化和突变,产生对哇巴因的抗性。转化是比突变更频繁发生的事件,转化与突变频率的比值在 24 到 1118 之间变化。另一种烃类衍生物,苯并[a]芘衍生的 9,10-二醇-7,8-氧化物,在不引起转化的情况下也能诱导哇巴因抗性。诱导产生的哇巴因抗性克隆并不表现出转化细胞的特征,而转化细胞也不表现出哇巴因抗性。这些发现的意义将被讨论。