Goerttler K, Loehrke H, Hesse B, Milz A, Schweizer J
Carcinogenesis. 1981;2(11):1087-94. doi: 10.1093/carcin/2.11.1087.
The tumor spectrum and tumor incidence in organs other than the skin were investigated in the 12-O-tetradecanoylphorbol-13-acetate (TPA) treated F 1-generation of 13 groups of NMRI mice which had been initiated by a single intragastric dose of 7,12-dimethylbenz[a]anthracene during days 6, 8, and 10--20 of pregnancy. Promotion by topical application of TPA to the back skin was carried out twice per week 12 weeks after birth over a period of 26 weeks. The forestomach epithelium represented the only organ in which statistically significant 2-stage carcinogenesis could be demonstrated. A promotion effect could be seen in tumors of the Harderian gland, of the liver of male animals and on the development of both benign and malignant tumors of the lung in both sexes. Promotion treatment therefore led to an activation of initiated tumor cells in those organs in which a very sensitive, more or less narrowly spaced oncogenic determination period exists.
在孕期第6、8和10 - 20天经单次胃内给予7,12 - 二甲基苯并[a]蒽启动的13组NMRI小鼠的F1代中,研究了12 - O - 十四酰佛波醇 - 13 - 乙酸酯(TPA)处理后皮肤以外器官的肿瘤谱和肿瘤发生率。出生后12周开始,每周两次在背部皮肤局部涂抹TPA进行促癌,持续26周。前胃上皮是唯一能证明有统计学意义的两阶段致癌作用的器官。在哈德氏腺肿瘤、雄性动物肝脏肿瘤以及两性肺部良性和恶性肿瘤的发生发展中可观察到促癌作用。因此,促癌治疗导致了那些存在非常敏感、致癌决定期或多或少间隔较窄的器官中已启动的肿瘤细胞的激活。