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表睾酮在激素依赖性前列腺肿瘤模型中的活性。

The activity of epitestosterone in hormone dependent prostate tumour models.

作者信息

Maucher A, von Angerer E, Hampl R, Stárka L

机构信息

Institut für Pharmazie, Universität Regensburg, Germany.

出版信息

Endocr Regul. 1994 Mar;28(1):23-9.

PMID:7949009
Abstract

Epitestosterone has been shown previously to counteract the testosterone activity in some experimental models. In the present study the activity of epitestosterone in an in vitro model of human LNCaP/FCS prostate cells and in vitro in Dunning R 3327-GH rat prostate carcinoma was tested. In LNCaP/FGC cells cultivated with fetal calf serum (FCS) treated with dextran-coated charcoal epitestosterone displayed rather androgenic than antiandrogenic properties, whereas the cultivation with native FCS resulted in a very weak inhibition of tumour cell growth with epitestosterone in higher concentration. The growth of Dunning R 3327-GH carcinoma of prostate was very weakly enhanced by epitestosterone alone as late as at the end of the 5-week experiment. Epitestosterone did not significantly inhibit the testosterone stimulated tumour growth.

摘要

此前已有研究表明,在某些实验模型中,表睾酮可抵消睾酮的活性。在本研究中,对表睾酮在人LNCaP/FCS前列腺细胞体外模型以及邓宁R 3327-GH大鼠前列腺癌体外模型中的活性进行了测试。在用葡聚糖包被活性炭处理的胎牛血清(FCS)培养的LNCaP/FGC细胞中,表睾酮表现出雄激素特性而非抗雄激素特性,而用天然FCS培养时,较高浓度的表睾酮对肿瘤细胞生长的抑制作用非常微弱。仅表睾酮对邓宁R 3327-GH前列腺癌生长的促进作用很弱,直到5周实验结束时才有所体现。表睾酮并未显著抑制睾酮刺激的肿瘤生长。

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