Allison D C, Bose K K, Anderson S, Curley S, Robertson J
Department of Surgery and Oncology, Johns Hopkins Medical School, Baltimore, Maryland 21205.
Cancer Res. 1989 Mar 15;49(6):1456-64.
MCa-11 tumor cells in exponential monolayer cultures were pulse/chase-labeled with [3H]thymidine and then regrown in fresh, plateau-fed, or starved medium. We measured the DNA content and autoradiographic labeling of these cells by absorption cytophotometry at intervals of 0, 2, 4, 8, 12, and 24 h to follow the progress through the cell cycle of those cells which had incorporated isotope. We found that for the cells grown in plateau-fed and starved medium the G0/G1, S, and G2 phases of the cell cycle were prolonged when compared to those for cells grown in fresh medium. These results show that, under adverse microenvironmental conditions, the growth of tumor cells can be regulated in all phases of the cell cycle, and that this regulation can include lengthening and even cessation of replicative DNA synthesis.
处于指数生长阶段的单层培养的MCa - 11肿瘤细胞用[³H]胸腺嘧啶核苷进行脉冲/追踪标记,然后在新鲜、稳定营养供应或饥饿培养基中再生长。我们每隔0、2、4、8、12和24小时通过吸收细胞光度法测量这些细胞的DNA含量和放射自显影标记,以追踪那些已掺入同位素的细胞在细胞周期中的进展。我们发现,与在新鲜培养基中生长的细胞相比,在稳定营养供应和饥饿培养基中生长的细胞,其细胞周期的G0/G1、S和G2期都延长了。这些结果表明,在不利的微环境条件下,肿瘤细胞的生长在细胞周期的所有阶段都可以受到调控,并且这种调控可以包括复制性DNA合成的延长甚至停止。