Doihara H, Takashima S, Saeki H, Takiyama W, Kurita A, Soga H, Tanada M, Yokoyama N, Moriwaki S
Dept. of Surgery, Shikoku Cancer Center Hospital, Matsuyama, Japan.
Gan To Kagaku Ryoho. 1990 Oct;17(10):2057-62.
Effect of medroxyprogesterone acetate (MPA) on the breast cancer cell kinetics was investigated by flow cytometry on paraffin-embedded tissues. Nuclear DNA contents were measured in 67 primary cases. MPA, 1,2000 mg/day, was administered orally for two weeks in 12 cases (MPA group) and the remaining cases (n-MPA group) served as the controls, until the day before operation. The DNA histograms were compared between both groups. The mean percentage of G0 + G1 phase was higher and that of S-phase and G2 + M phase, lower, in the MPA group than those in the n-MPA group. Especially in estrogen receptor positive and premenopausal cases, a significant difference was present between both groups. These results suggest that MPA could inhibit DNA synthesis with a delay of the cell cycle progression in human breast cancer.
通过流式细胞术对石蜡包埋组织进行研究,以探讨醋酸甲羟孕酮(MPA)对乳腺癌细胞动力学的影响。对67例原发性病例测量了核DNA含量。12例患者(MPA组)口服MPA,剂量为1200mg/天,持续两周,其余病例(非MPA组)作为对照,直至手术前一天。比较了两组的DNA直方图。MPA组G0 + G1期的平均百分比高于非MPA组,S期和G2 + M期的平均百分比则低于非MPA组。特别是在雌激素受体阳性的绝经前病例中,两组之间存在显著差异。这些结果表明,MPA可以抑制DNA合成,并延缓人乳腺癌细胞周期的进程。