Kinzel V, Richards J, Stöhr M
Cancer Res. 1981 Jan;41(1):300-5.
Within 24 hr after incubation of synchronous HeLa cell cultures with small nontoxic doses of the tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA; 10(-7) or 10(-8) M), a variety of transient alterations in the cell cycle traverse was detected by different techniques. The measurement of thymidine incorporation rates into DNA, of labeling and mitotic indices, and of flow cytometry revealed (a) an inhibition of cells in G1 shortly prior to their entering S phase, (b) a reduced rate of DNA synthesis and a delayed passage of cells through S phase which were in this phase on addition of TPA, (c) a delayed passage through G2 of a portion of cells which were somewhere in the first half of the S phase on addition of TPA, and (d) an instant but short-lasting blockage in G2 immediately before mitosis. The effects of TPA are reminiscent of published results on X-irradiated cell cultures. None of these effects was noticed with the hyperplasiogenic but nonpromoting phorbol ester 4-O-methyl-12-O-tetradecanoylphorbol-13-acetate (10(-6) M). The data were confirmed by experiments with synchronized HeLa cells as described in an accompanying paper.
用小剂量无毒的肿瘤启动子12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA;10⁻⁷或10⁻⁸M)处理同步化的HeLa细胞培养物24小时内,通过不同技术检测到细胞周期进程中出现了多种短暂变化。对DNA中胸苷掺入率、标记指数和有丝分裂指数的测量以及流式细胞术分析显示:(a)处于G1期的细胞在进入S期前不久受到抑制;(b)DNA合成速率降低,添加TPA时处于S期的细胞通过S期的时间延迟;(c)添加TPA时处于S期前半段某个位置的一部分细胞通过G2期的时间延迟;(d)在有丝分裂前G2期立即出现瞬间但短暂的阻滞。TPA的这些作用让人想起已发表的关于X射线照射细胞培养物的结果。用增生性但无启动作用 的佛波醇酯4 - O - 甲基 - 12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(10⁻⁶M)处理时未观察到这些作用。如随附论文所述,用同步化的HeLa细胞进行的实验证实了这些数据。