Solt D B, Cayama E, Sarma D S, Farber E
Cancer Res. 1980 Apr;40(4):1112-8.
The administration of either N-nitrosodiethylamine (diethyl-nitrosamine) to intact male F-344 rats or N-methyl-N-nitrosourea to similar animals 18 hr after partial hepatectomy results in the induction of altered resistant hepatocytes that persist for up to 36 weeks with no perceptible decrease in their number. The criterion for resistance was the ability to proliferate rapidly and to develop into foci or nodules when exposed to a level of dietary 2-acetylaminofluorene that inhibits the proliferation of the vast majority of hepatocytes when liver cell proliferation is stimulated by surgical or chemical partial hepatectomy. Since this selection procedure, when coupled with a single dose of diethylnitrosamine, is associated with a high incidence of liver cancer as compared to appropriate controls, and since similar foci and nodules were shown previously to be one site of origin for hepatocellular carcinoma in this model, the induction of resistant hepatocytes is interpreted as initiation. Thus, these results suggest that initiation of liver carcinogenesis in this model is irreversible, at least for a period of 36 weeks.
给完整的雄性F - 344大鼠注射N - 亚硝基二乙胺(二乙基亚硝胺),或在部分肝切除术后18小时给类似的动物注射N - 甲基 - N - 亚硝基脲,会诱导产生抗性改变的肝细胞,这些细胞可持续长达36周,数量没有明显减少。抗性的标准是当暴露于一定水平的膳食2 - 乙酰氨基芴时能够快速增殖并发展为病灶或结节,而当通过手术或化学性部分肝切除术刺激肝细胞增殖时,该水平的2 - 乙酰氨基芴会抑制绝大多数肝细胞的增殖。由于与适当的对照组相比,这种选择程序与单剂量二乙基亚硝胺联合使用时肝癌的发生率较高,并且由于之前在该模型中已证明类似的病灶和结节是肝细胞癌的一个起源部位,因此抗性肝细胞的诱导被解释为启动。因此这些结果表明,在该模型中肝癌发生的启动是不可逆的,至少在36周的时间内是不可逆的。