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丙酸睾酮和/或己烯雌酚间歇给药对3,2'-二甲基-4-氨基联苯引发的大鼠前列腺癌发生有轻微促进作用。

Slight promotion effects of intermittent administration of testosterone propionate and/or diethylstilbestrol on 3,2'-dimethyl-4-aminobiphenyl-initiated rat prostate carcinogenesis.

作者信息

Cui L, Mori T, Takahashi S, Imaida K, Akagi K, Yada H, Yaono M, Shirai T

机构信息

First Department of Pathology, Nagoya City University Medical School, Nagoya, Japan.

出版信息

Cancer Lett. 1998 Jan 9;122(1-2):195-9. doi: 10.1016/s0304-3835(97)00390-x.

Abstract

In order to determine the effects of intermittent hormonal manipulation on the promotion stage of rat prostate carcinogenesis, testosterone and/or estrogen were administered to F344 rats for 40 weeks after 20-weeks treatment with the prostate carcinogen, 3,2'-dimethyl-4-aminobiphenyl. For this purpose testosterone propionate (TP) and diethylstilbestrol (DES) were introduced into silastic tubes, 2- and 0.5-cm long, respectively, and implanted into the subcutis for seven repeated cycles of 30 days treatment and 10 days withdrawal. Intermittent administration of TP resulted in suppression of ventral prostate adenocarcinoma development and slight but non-significant increases in the incidences of invasive carcinomas of the lateral prostate and seminal vesicles. Intermittent administration of DES completely suppressed tumorigenesis in all sites and the combination of TP and DES generally inhibited prostate tumor development. Thus, under the present experimental conditions, no strong enhancing effects of cyclic hormonal manipulation were observed on rat prostate carcinogenesis. Indeed, the opposite appeared to be the case.

摘要

为了确定间歇性激素处理对大鼠前列腺癌发生促进阶段的影响,在用前列腺致癌物3,2'-二甲基-4-氨基联苯处理20周后,对F344大鼠给予睾酮和/或雌激素,持续40周。为此,将丙酸睾酮(TP)和己烯雌酚(DES)分别放入2厘米和0.5厘米长的硅橡胶管中,植入皮下,进行7个重复周期的处理,每个周期包括30天给药和10天停药。间歇性给予TP可抑制腹侧前列腺腺癌的发展,同时使外侧前列腺和精囊浸润性癌的发生率略有增加,但无统计学意义。间歇性给予DES可完全抑制所有部位的肿瘤发生,TP与DES联合使用通常可抑制前列腺肿瘤的发展。因此,在本实验条件下,未观察到周期性激素处理对大鼠前列腺癌发生有强烈的促进作用。事实上,情况似乎恰恰相反。

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