Osborne C K, Boldt D H, Clark G M, Trent J M
Cancer Res. 1983 Aug;43(8):3583-5.
We have studied the effects of tamoxifen on the cell cycle kinetics of the endocrine-responsive MCF-7 human breast cancer cells. Tamoxifen inhibits proliferation of MCF-7 cells. The tritiated thymidine labeling index is markedly reduced by tamoxifen, indicating a reduction in the fraction of cells in S phase. Flow cytometry of mithramycin-stained cells reveals that cells accumulate in G1 phase, with a concomitant depletion of S- and G2-M-phase cells with tamoxifen. Mapping of G1-phase cells by morphology of prematurely condensed chromosomes demonstrated that tamoxifen-treated cells accumulate in early G1. These studies indicate that tamoxifen inhibits proliferation of MCF-7 human breast cancer cells by invoking a transition delay early in the G1 phase of the cell cycle.
我们研究了他莫昔芬对内分泌反应性MCF-7人乳腺癌细胞的细胞周期动力学的影响。他莫昔芬抑制MCF-7细胞的增殖。他莫昔芬显著降低了氚标记胸腺嘧啶核苷标记指数,表明S期细胞比例减少。对光神霉素染色细胞进行的流式细胞术分析显示,细胞在G1期积累,同时他莫昔芬处理导致S期和G2-M期细胞减少。通过早熟凝集染色体的形态对G1期细胞进行定位显示,经他莫昔芬处理的细胞在G1早期积累。这些研究表明,他莫昔芬通过在细胞周期的G1期早期引起转换延迟来抑制MCF-7人乳腺癌细胞的增殖。