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非甾体类抗雌激素药物与性类固醇激素联合作用对组织培养中大鼠子宫腺癌细胞生长的影响

The combined effect of nonsteroidal anti-oestrogens and sex steroids on the growth of rat uterine adenocarcinoma cells in tissue culture.

作者信息

Sekiya S, Takamizawa H

出版信息

Br J Obstet Gynaecol. 1976 Mar;83(3):183-6. doi: 10.1111/j.1471-0528.1976.tb00806.x.

Abstract

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.

摘要

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。

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