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17β-雌二醇对体外辐射转化的影响;蛋白酶抑制剂对其影响的抑制作用。

Effects of 17 beta-estradiol on radiation transformation in vitro; inhibition of effects by protease inhibitors.

作者信息

Kennedy A R, Weichselbaum R R

出版信息

Carcinogenesis. 1981;2(1):67-9. doi: 10.1093/carcin/2.1.67.

Abstract

We have investigated the effects of 17 beta-estradiol, given both alone and with X-irradiation, on the induction of malignant transformation in vitro. Treatment with 10(-6)M 17 beta-estradiol for 6 weeks, or 10(-5)M 17 beta-estradiol for only 5 days, induced malignant transformation in C3H 10T1/2 cells. Estradiol also acted as a cocarcinogen for X-ray induced transformation; the results indicate an additive effect when the cells were exposed to both agents together. The protease inhibitors antipain and leupeptin suppressed estradiol induced transformation as well as the additive effect observed for estradiol-radiation transformation.

摘要

我们研究了单独给予17β-雌二醇以及联合X射线照射,对体外诱导恶性转化的影响。用10⁻⁶M 17β-雌二醇处理6周,或仅用10⁻⁵M 17β-雌二醇处理5天,均可诱导C3H 10T1/2细胞发生恶性转化。雌二醇还可作为X射线诱导转化的促癌剂;结果表明,当细胞同时暴露于这两种因素时,存在相加效应。蛋白酶抑制剂抗痛素和亮抑酶肽可抑制雌二醇诱导的转化以及雌二醇-辐射转化中的相加效应。

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