雌激素在20-甲基胆蒽诱导小鼠子宫肿瘤中的协同作用[摘要]。

B V Hall, Balder Rb, K Hamilton
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引用次数: 0

摘要

采用环针法切除幼龄和成年CF1小鼠200只,双侧子宫角植入约2 mg甲基胆蒽(MCA)。然后在0.05 ml油中皮下注射20微克己烯雌酚,每周3次,等量组,连续注射0、4、6、10、12、14、16、18和20周。所有动物均于MCA植入后180天死亡或牺牲。57只小鼠在雌激素治疗中存活并在MCA植入后存活至少100天,其中近一半的小鼠发生了子宫肿瘤。大多数受影响的小鼠在两个角膜上都出现了肿瘤。长期接受雌激素治疗的小鼠的肿瘤特别大且具有侵袭性。组织学上以肉瘤为主,但诱导腺癌的比例约为1:4。用雌激素治疗12-20周的小鼠肿瘤发生率明显高于用雌激素治疗4-10周的小鼠。8只小鼠在双侧MCA植入和4周内皮下注射60 mcg己烯雌酚12次后存活102 ~ 168天,仅1例子宫肿瘤突出。己烯雌酚在服用足够长的时间后,似乎在小鼠中作为一种辅助致癌物质,加速MCA诱导子宫肿瘤的发生,并可能刺激其生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The co-action of estrogen in the induction of tumors of the mouse uterus treated with 20-methylcholanthrene [abstract].

Over 200 young mature and mature CF1 mice were ovariectomized and their uterine horns implanted bilaterally with circa 2 mg methylcholanthrene (MCA) by trocar. Subcutaneous injections of 20 mcg diethylstilbestrol in 0.05 ml oil were then made 3x weekly in equivalent groups for 0, 4, 6, 10, 12, 14, 16, 18, and 20 weeks. All animals died or were sacrificed by 180 days following MCA implantation. Nearly 1/2 of the 57 mice surviving estrogen treatment and living at least 100 days after MCA implantation developed uterine tumors. Most of the affected mice developed tumors in both cornua. Tumors in mice receiving estrogen for the longer periods were especially large and aggressive. Histologically, they were predominantly sarcomatous, but adenocarcinomas were induced in the approximate ratio of 1:4. The incidence of tumors in mice treated with estrogens for 12-20 weeks was significantly higher than in those given extrogen 4-10 weeks. Only 1 prominent uterine tumor was found in 8 mice which survived 102-168 days after bilateral MCA implantation and 12 subcutaneous injections of 60 mcg diethylstilbestrol in 4 weeks. Diethylstilbestrol, when administered for a sufficient period, seemingly acts as a cocarcinogen in mice, accelerating the induction of uterine tumors by MCA and perhaps stimulating their growth.

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