Sekiya S, Takamizawa H
Br J Obstet Gynaecol. 1976 Mar;83(3):183-6. doi: 10.1111/j.1471-0528.1976.tb00806.x.
Nonsteroidal anti-oestrogenic drugs, tamoxifen and clomiphene citrate, at concentrations higher than 0.001 mug/ml reduced the colony forming ability of cells derived from a rat uterine adenocarcinoma in vitro. The 50 per cent inhibitory dose of these drugs was about one-hundredth of that of sex steroids. When the cells were treated with combinations of these nonsteroidal anti-oestrogenic drugs and the 50 per cent inhibitory dose (8 mug/ml) of progesterone, a synergistic effect on the inhibition of colony formation was observed. In contrast to progesterone, oestradiol-17beta (the 50 per cent inhibitory dose of which was about 16 mug/ml) suppressed additively the colony formation only in combination with low doses of anti-oestrogenic drugs.
非甾体类抗雌激素药物他莫昔芬和枸橼酸氯米芬,浓度高于0.001微克/毫升时,可降低体外培养的大鼠子宫腺癌细胞的集落形成能力。这些药物的半数抑制剂量约为性甾体激素的百分之一。当用这些非甾体类抗雌激素药物与孕酮的半数抑制剂量(8微克/毫升)联合处理细胞时,观察到对集落形成的抑制有协同作用。与孕酮相反,17β-雌二醇(其半数抑制剂量约为16微克/毫升)仅在与低剂量抗雌激素药物联合使用时,对集落形成有相加性抑制作用。