Slaga T J, Fischer S M, Nelson K, Gleason G L
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3659-63. doi: 10.1073/pnas.77.6.3659.
The effects of nonpromoting and weakly promoting diterpenes on skin tumor promotion by 12-O-tetradecanoylphorbol 13-acetate (TPA) were investigated. When phorbol and phorbol 12,13-diacetate (both nonpromoting) were given simultaneously with TPA after 7,12-dimethylbenz[a]-anthracene (DMBA) initiation in female mice, they had no effect on TPA promotion. However, the nonpromoter 4-O-methyl-TPA and the weak promoter mezerein were found to inhibit TPA promotion in a dose-dependent manner when given simultaneously with TPA. Because mezerein was found to be an effective inhibitor of TPA promotion when given simultaneously and because it induces many biological responses similar to those to TPA, the capacity of mezerein to act as an incomplete promoter in a two-stage promotion protocol was also investigated. Twice-weekly applications of 1,2, or 5 mug of TPA for 2 weeks after DMBA initiation produced 0, 0, and 0.5 papilloma per mouse, respectively, at 20 weeks. When the twice-weekly applications of TPA for 2 weeks were followed by twice-weekly treatments with 2 mug of mezerein for 18 weeks, the number of papillomas per mouse was 2.2, 3.5, and 9.0, respectively. Twice-weekly applications of 2 mug of TPA for 2 weeks followed by twice-weekly treatments with 1, 2, or 4 mug of mezerein for 18 weeks produced 2.1, 3.5, and 6.8 papillomas per mouse, respectively, in DMBA-treated mice. Twice-weekly doses as high as 40 mug of 4-O-methyl-TPA were not effective in producing tumors when given after a limited treatment with TPA; however, 4-O-methyl-TPA had weak activity as a first-stage promoter. The results suggest that although mezerein by itself is a weak promoter and mimics TPA in many biochemical and morphological effects it is a potent second-stage promoter in a two-stage promotion regimen.
研究了非促癌和弱促癌二萜类化合物对12-O-十四烷酰佛波醇-13-乙酸酯(TPA)诱导皮肤肿瘤促癌作用的影响。在雌性小鼠经7,12-二甲基苯并[a]蒽(DMBA)启动后,当佛波醇和佛波醇12,13-二乙酸酯(均为非促癌剂)与TPA同时给药时,它们对TPA的促癌作用没有影响。然而,发现非促癌剂4-O-甲基-TPA和弱促癌剂芫花酯素与TPA同时给药时,能以剂量依赖的方式抑制TPA的促癌作用。由于发现芫花酯素与TPA同时给药时是TPA促癌作用的有效抑制剂,且它能诱导许多与TPA相似的生物学反应,因此还研究了芫花酯素在两阶段促癌方案中作为不完全促癌剂的能力。在DMBA启动后,每周两次分别给予1、2或5μg TPA,持续2周,在20周时每只小鼠分别产生0、0和0.5个乳头瘤。当每周两次给予TPA 2周后,接着每周两次给予2μg芫花酯素,持续18周,每只小鼠的乳头瘤数量分别为2.2、3.5和9.0个。在DMBA处理的小鼠中,每周两次给予2μg TPA 2周后,接着每周两次分别给予1、2或4μg芫花酯素,持续18周,每只小鼠分别产生2.1、3.5和6.8个乳头瘤。在TPA进行有限处理后,每周两次给予高达40μg的4-O-甲基-TPA不能有效诱导肿瘤;然而,4-O-甲基-TPA作为第一阶段促癌剂活性较弱。结果表明,尽管芫花酯素本身是一种弱促癌剂,在许多生化和形态学效应上模拟TPA,但在两阶段促癌方案中它是一种有效的第二阶段促癌剂。