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脱氢表雄酮(DHEA)和3β-甲基雄甾-5-烯-17-酮:7,12-二甲基苯并[a]蒽(DMBA)引发及12-O-十四烷酰佛波醇-13-乙酸酯(TPA)促进的小鼠皮肤乳头瘤形成的抑制剂。

Dehydroepiandrosterone (DHEA) and 3 beta-methylandrost-5-en-17-one: inhibitors of 7,12-dimethylbenz[a]anthracene (DMBA)-initiated and 12-O-tetradecanoylphorbol-13-acetate (TPA)-promoted skin papilloma formation in mice.

作者信息

Pashko L L, Rovito R J, Williams J R, Sobel E L, Schwartz A G

出版信息

Carcinogenesis. 1984 Apr;5(4):463-6. doi: 10.1093/carcin/5.4.463.

Abstract

Long-term oral administration of the adrenal steroid, dehydroepiandrosterone (DHEA), has previously been shown to inhibit the development of spontaneous breast cancer and chemically induced lung and colon tumors in various mouse strains. In the two-stage skin papilloma system in the mouse, topical application of DHEA inhibits both 7,12-dimethylbenz[a]anthracene initiation and 12-O-tetradecanoylphorbol-13-acetate promotion of these tumors. The synthetic steroid, 3 beta-methylandrost-5-en-17-one, which, unlike DHEA, is not demonstrably estrogenic in the rat, also inhibits papilloma development.

摘要

先前的研究表明,长期口服肾上腺类固醇脱氢表雄酮(DHEA)可抑制多种小鼠品系中自发性乳腺癌以及化学诱导的肺癌和结肠癌的发生。在小鼠的两阶段皮肤乳头状瘤系统中,局部应用DHEA可抑制7,12-二甲基苯并[a]蒽引发的肿瘤以及12-O-十四酰佛波醇-13-乙酸酯促进的这些肿瘤。合成类固醇3β-甲基雄甾-5-烯-17-酮,与DHEA不同,在大鼠中未表现出明显的雌激素活性,也可抑制乳头状瘤的发展。

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