O'Brien T G, Simsiman R C, Boutwell R K
Cancer Res. 1975 Sep;35(9):2426-33.
The induction of ornithine decarboxylase and S-adenosyl-L-methionine decarboxylase in mouse epidermis by various classes of tumor-promoting and nonpromoting compounds has been studied in order to determine the specificity of this response for tumor promotion. The effect of topical applications of a series of phorbol esters on these enzyme activities correlated well with their promoting abilities. Iodoacetic acid, anthralin, and Tween 60, all promoting compounds, also stimulated both of these enzyme activities after single and multiple applications. The hyperplastic agents acetic acid, cantharidin, and ethyl phenylpropriolate, however, had little effect on ornithine decarboxylase activity but a pronounced effect on epidermal S-adenosyl-L-methionine decarboxylase activity. The specificity of the ornithine decarboxylase response for tumor promotion was suggested by the results of the above experiments as well as the stimulatory effect of a completely carcinogenic dose of 7,12-dimethylbenz[a]anthracene; a lower initiating dose had no effect. In addition, epidermal tumors produced by a two-stage procedure showed consistently high levels of ornithine decarboxylase activity but variable levels of S-adenosyl-L-methionine decarboxylase activity.
为了确定小鼠表皮中鸟氨酸脱羧酶和S-腺苷-L-甲硫氨酸脱羧酶对肿瘤促进反应的特异性,研究了各类促癌和非促癌化合物对它们的诱导作用。一系列佛波酯局部应用对这些酶活性的影响与其促癌能力密切相关。碘乙酸、蒽林和吐温60,所有促癌化合物,单次和多次应用后也刺激了这两种酶的活性。然而,增生剂乙酸、斑蝥素和乙基苯丙炔酸对鸟氨酸脱羧酶活性影响很小,但对表皮S-腺苷-L-甲硫氨酸脱羧酶活性有显著影响。上述实验结果以及完全致癌剂量的7,12-二甲基苯并[a]蒽的刺激作用表明了鸟氨酸脱羧酶反应对肿瘤促进的特异性;较低的起始剂量没有影响。此外,通过两阶段程序产生的表皮肿瘤始终显示出高水平的鸟氨酸脱羧酶活性,但S-腺苷-L-甲硫氨酸脱羧酶活性水平各不相同。