Peterson A R, Mondal S, Brankow D W, Thon W, Heidelberger C
Cancer Res. 1977 Sep;37(9):3223-7.
The synthesis of DNA has been studied by autoradiography and by measurements of tritiated thymidine ([3H]TdR) incorporation in cultured C3H/10T1/2 mouse embryo fibroblasts. The cells were first treated with 3-methylcholanthrene as an initiator and then with promoters according to schedules that produce oncogenic transformation. The levels of 3-methylcholanthrene used did not affect the growth or [3H]TdR incorporation of the cells. Treatment during the log phase of growth with 12-O-tetradecanoyl-phorbol-13-acetate, phorbol didecanoate, or 4alpha-phorbol didecanoate produced a transient inhibition of [3H]TdR incorporation with the maximum at 12 hr after treatment. This resulted in a temporary delay of growth followed by recovery of the normal cell-doubling time. Phorbol did not produce these effects, suggesting that the inhibition of DNA synthesis is associated with the process of promotion. Although treatment of the cells with 12-O-tetradecanoyl-phorbol-13-acetate during stationary phase resulted in a 2- to 3-fold stimulation of [3H]TdR incorporation, multiple treatments spanning log and stationary phases were found to be necessary for promotion.
通过放射自显影以及对氚标记胸腺嘧啶核苷([3H]TdR)掺入培养的C3H/10T1/2小鼠胚胎成纤维细胞的情况进行测量,对DNA合成进行了研究。首先用3-甲基胆蒽作为引发剂处理细胞,然后根据产生致癌转化的时间表用促癌剂处理。所用3-甲基胆蒽的剂量不影响细胞的生长或[3H]TdR掺入。在对数生长期用12-O-十四烷酰佛波醇-13-乙酸酯、佛波醇二癸酸酯或4α-佛波醇二癸酸酯处理,会产生[3H]TdR掺入的短暂抑制,在处理后12小时达到最大值。这导致生长暂时延迟,随后恢复正常的细胞倍增时间。佛波醇不会产生这些效应,表明DNA合成的抑制与促癌过程有关。尽管在静止期用12-O-十四烷酰佛波醇-13-乙酸酯处理细胞会导致[3H]TdR掺入增加2至3倍,但发现跨越对数期和静止期的多次处理对于促癌是必要的。