Thomas M, Monet J D
Laboratoire TIM3-USR CNRS B690/Equipe de Reconnaissance des Formes et Microscopie Quantitative, Université Joseph Fourier, Grenoble, France.
J Clin Endocrinol Metab. 1992 Sep;75(3):865-70. doi: 10.1210/jcem.75.3.1517379.
The antiproliferative effect of RU486 and its effect combined with tamoxifen on the growth and cell cycle kinetics parameters on the MCF-7 human carcinoma cells were investigated. When MCF-7 cells in the exponential growth phase were treated with RU486 (10(2) nmol/L), a time-dependent cell growth inhibition was observed which was significant 5 days after the beginning of treatment. This inhibition was accompanied by a time- and dose-dependent decrease in the percentage of S and G2-M phase cells and a concomitant increase in the percentage of cells in the G0/G1 phase of the cell cycle. With tamoxifen (10(5) pmol/L), growth inhibition was obtained after 4 days of treatment of cells, and the blockage of the cell cycle occurred in the G0/G1 phase. In the case of simultaneous treatment of MCF-7 cultures with RU486 (10(2) nmol/L) and tamoxifen (10(5) pmol/L), we observed a synergistic inhibitory effect on the proliferative rate for short treatment (less than or equal to 3 days), whereas RU486 or tamoxifen alone had no effect. For the intermediate treatment (4 days), the combined effect of RU486 and tamoxifen was not significant compared to the effect of tamoxifen alone. For the long treatment (greater than 4 days), there were no differences between the number of cells in the treated cultures under different experimental conditions, but all were inhibited compared to those in control cell cultures. This simultaneous treatment of cells does not induce any change in the distribution of cells in the different cell cycle phases compared to tamoxifen percentages. These results suggest that RU486 is a cell cycle phase-specific growth inhibitory agent, and a combination of antiestrogen/antiprogestin should be considered as a possible improvement in breast cancer endocrine therapy.
研究了RU486的抗增殖作用及其与他莫昔芬联合使用对MCF-7人癌细胞生长和细胞周期动力学参数的影响。当处于指数生长期的MCF-7细胞用RU486(10² nmol/L)处理时,观察到细胞生长受到时间依赖性抑制,在处理开始后5天显著。这种抑制伴随着S期和G2-M期细胞百分比的时间和剂量依赖性下降以及细胞周期G0/G1期细胞百分比的相应增加。用他莫昔芬(10⁵ pmol/L)处理细胞4天后获得生长抑制,细胞周期阻滞发生在G0/G1期。在MCF-7培养物同时用RU486(10² nmol/L)和他莫昔芬(10⁵ pmol/L)处理的情况下,我们观察到短期处理(小于或等于3天)对增殖率有协同抑制作用,而单独使用RU486或他莫昔芬则没有效果。对于中期处理(4天),与单独使用他莫昔芬的效果相比,RU486和他莫昔芬的联合效果不显著。对于长期处理(大于4天),不同实验条件下处理培养物中的细胞数量没有差异,但与对照细胞培养物相比均受到抑制。与他莫昔芬百分比相比,这种细胞同时处理不会导致不同细胞周期阶段的细胞分布发生任何变化。这些结果表明,RU486是一种细胞周期阶段特异性生长抑制剂,抗雌激素/抗孕激素联合应用应被视为乳腺癌内分泌治疗的一种可能改进方法。