Topping D C, Nettesheim P
J Natl Cancer Inst. 1980 Sep;65(3):627-30.
The cocarcinogenic effect of chrysotile asbestos was investigated in heterotopic tracheal transplants of F344 rats. Tracheal transplants were first exposed to graded doses of dimethylbenz[a]anthracene (DMBA) contained in intraluminal pellets. The doses ranged from 12.5 to 100 micrograms. Control tracheas received blank pellets. Four weeks after the start of DMBA exposure (when all carcinogen had been released from the pellets), the spent pellets were removed, and 200 micrograms chrysotile, a nontumorigenic dose of asbestos, was introduced into the lumina of the preexposed tracheas. No significant enhancement of the tumor response was seen with 100 micrograms DMBA, a dose that was tumorigenic by itself. However, with 50 and 25 micrograms DMBA, nontumorigenic dose levels, a 15 and 23% incidence of tracheal carcinomas occurred when DMBA exposure was followed by a nontumorigenic dose of chrysotile. At 12.5 micrograms DMBA, this effect was not observed. Whatever the mechanisms were that formed the basis of this tumor enhancement effect of asbestos, the consequences were similar to those observed with tumor promotion in classical two-stage carcinogenesis studies.
在F344大鼠的异位气管移植实验中研究了温石棉的促癌作用。气管移植体首先暴露于腔内小丸中不同剂量的二甲基苯并[a]蒽(DMBA)。剂量范围为12.5至100微克。对照气管接受空白小丸。DMBA暴露开始四周后(此时所有致癌物已从小丸中释放),取出用过的小丸,并将200微克温石棉(一种非致瘤剂量的石棉)引入预先暴露的气管腔内。100微克DMBA本身具有致瘤性,但未观察到肿瘤反应有明显增强。然而,对于50微克和25微克DMBA(非致瘤剂量水平),在DMBA暴露后给予非致瘤剂量的温石棉时,气管癌的发生率分别为15%和23%。在12.5微克DMBA时,未观察到这种效应。无论石棉这种肿瘤增强效应的形成机制是什么,其结果与经典两阶段致癌研究中观察到的肿瘤促进作用相似。