Kinzel V, Richards J, Stöhr M
Cancer Res. 1981 Jan;41(1):306-9.
A flow cytometric study was carried out on the effects of tumor-promoting 12-O-tetradecanoylphorbol-13-acetate (TPA; 10(-8) M) on HeLa cells synchronized by amethopterin for DNA synthesis. Cells treated with TPA at the time of release from the amethopterin block showed a delayed passage through S phase and partially through G2 in their immediate life span as measured 24 hr after release. This late G2 delay was not observed when TPA was added to cells during late S or G2 phase. In this case, however, a direct inhibition of cells in G2 became evident as observed about 15 hr after release from block. None of these effects was caused by the nonpromoting 4-O-methyl-12-O-tetradecanoylphorbol-13-acetate (10(-6) M). These data support observations obtained with asynchronous cultures. The TPA effects resemble those reported after X-irradiation of cell cultures.
进行了一项流式细胞术研究,以探讨促肿瘤剂12-O-十四烷酰佛波醇-13-乙酸酯(TPA;10⁻⁸ M)对通过氨甲蝶呤同步化进行DNA合成的HeLa细胞的影响。在从氨甲蝶呤阻滞中释放时用TPA处理的细胞,在释放后24小时测量其直接寿命时,显示出通过S期的延迟以及部分通过G2期的延迟。当在S期晚期或G2期向细胞中添加TPA时,未观察到这种晚期G2期延迟。然而,在这种情况下,从阻滞中释放后约15小时观察到,对G2期细胞的直接抑制变得明显。这些效应均不是由非促肿瘤剂4-O-甲基-12-O-十四烷酰佛波醇-13-乙酸酯(10⁻⁶ M)引起的。这些数据支持了在非同步培养物中获得的观察结果。TPA的效应类似于细胞培养物经X射线照射后报道的效应。