Mondal S, Brankow D W, Heidelberger C
Cancer Res. 1976 Jul;36(7 PT 1):2254-60.
The initiation and promotion stages of chemical oncogenesis have been demonstrated in cultured C3H/10T1/2 mouse embryo cells. Treatment of the cells with a subeffective concentration of 3-methylcholanthrene, benzo(a)pyrene, or 7,12-dimethylbenz(a)anthracene, followed 4 days later by a nontransforming amount of tetradecanoylphorbol acetate (TPA), phorbol didecanoate, or 4-alpha-phorbol didecanoate, produced transformation. Phorbol was ineffective. TPA did not select for transformed cells. When TPA treatment preceded 3-methylcholanthrene, no enhancement of transformation was observed. When TPA was added immediately after hydrocarbon treatment, there was a significant inhibition of transformation. TPA did not exert promoting activity when the hydrocarbons were in high enough concentrations to produce appreciable transformation. The promoting action of TPA cannot be attributed only to a stimulation of cell division.
化学致癌作用的启动和促进阶段已在培养的C3H/10T1/2小鼠胚胎细胞中得到证实。用亚有效浓度的3-甲基胆蒽、苯并(a)芘或7,12-二甲基苯并(a)蒽处理细胞,4天后再用非转化量的十四酰佛波醇乙酸酯(TPA)、佛波醇二癸酸酯或4-α-佛波醇二癸酸酯处理,可导致细胞转化。佛波醇无效。TPA不会选择转化细胞。当TPA处理先于3-甲基胆蒽时,未观察到转化增强。当在烃处理后立即加入TPA时,转化受到显著抑制。当烃浓度足够高以产生明显转化时,TPA不发挥促进活性。TPA的促进作用不能仅归因于对细胞分裂的刺激。