Kuroki T, Chida K, Munakata K, Murakami Y
Biochem Biophys Res Commun. 1986 May 29;137(1):486-92. doi: 10.1016/0006-291x(86)91236-2.
Intracutaneous injection of cholera toxin into mice induced epidermal hyperplasia to a greater extent than 12-O-tetradecanoylphorbol-13-acetate. It also induced adenylate cyclase and though weakly, ornithine decarboxylase of the epidermis. Cholera toxin, however, showed no tumor promoting activity in mouse skin carcinogenesis. In the single stage promotion, cholera toxin (50 ng) was injected once a week for 10 weeks into the skin of SENCAR mice initiated with 25 micrograms 7,12-dimethylbenz[a]anthracene, but no tumors developed. In the two-stage promotion test, cholera toxin (10-100 ng) was injected for one or two weeks into the initiated skin and then mezerein (4 micrograms) was applied twice a week for 18 weeks, but the toxin did not increase incidence or numbers of papillomas.
将霍乱毒素皮内注射到小鼠体内,比12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯更能诱导表皮增生。它还能诱导腺苷酸环化酶,并且对表皮鸟氨酸脱羧酶的诱导作用较弱。然而,霍乱毒素在小鼠皮肤致癌过程中没有肿瘤促进活性。在单阶段促进实验中,将霍乱毒素(50纳克)每周一次注射到用25微克7,12 - 二甲基苯并[a]蒽启动的SENCAR小鼠皮肤中,持续10周,但未出现肿瘤。在两阶段促进实验中,将霍乱毒素(10 - 100纳克)注射到已启动的皮肤中一至两周,然后每周两次涂抹大戟二萜醇酯(4微克),持续18周,但该毒素并未增加乳头状瘤的发生率或数量。