Bhide S V, Munir K M, Wiessler M, Sarode A V, Soman C S
J Natl Cancer Inst. 1984 Sep;73(3):737-41.
An oral tumor model has been developed in inbred Syrian golden hamsters by continuous applications every 2 weeks of methyl(acetoxymethyl)nitrosamine [(DMN-OAC) CAS: 56856-83-8; methylnitrosaminomethyl ester acetic acid] at 2 mg/kg body weight alone or by a single application of DMN-OAC followed by continuous twice weekly applications of 12-O-tetradecanoylphorbol 13-acetate (TPA) (1 microgram/animal). Similar studies were done in the W rat buccal mucosa. In the hamsters treated continuously with DMN-OAC, 100% of the tumors were observed in the cheek pouch; none were observed at other sites. In contrast, in the rats treated similarly, only a 67% tumor incidence was observed, of which only 42% were oral tumors. A promoter effect of TPA was observed in hamster cheek pouch tumors induced by DMN-OAC, whereas rat oral mucosa did not respond to TPA treatment.
通过每2周以2mg/kg体重单独连续应用甲基(乙酰氧基甲基)亚硝胺[(DMN - OAC),化学物质登记号:56856 - 83 - 8;甲基亚硝胺甲基酯乙酸],或先单次应用DMN - OAC,随后每周两次连续应用12 - O - 十四烷酰佛波醇13 - 乙酸酯(TPA)(1微克/动物),在近交系叙利亚金仓鼠中建立了口腔肿瘤模型。在W大鼠颊黏膜上进行了类似研究。在连续用DMN - OAC处理的仓鼠中,100%的肿瘤出现在颊囊;在其他部位未观察到肿瘤。相比之下,在同样处理的大鼠中,仅观察到67%的肿瘤发生率,其中只有42%是口腔肿瘤。在由DMN - OAC诱导的仓鼠颊囊肿瘤中观察到TPA的促癌作用,而大鼠口腔黏膜对TPA处理无反应。