首页> 美国卫生研究院文献>British Journal of Cancer >Anti-tumour efficacy of calusterone against DMBA-induced rat mammary adenocarcinoma in vivo and in organ culture.
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Anti-tumour efficacy of calusterone against DMBA-induced rat mammary adenocarcinoma in vivo and in organ culture.

机译:钙黄酮在体内和器官培养物中对DMBA诱导的大鼠乳腺腺癌的抗肿瘤功效。

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摘要

The effect of calusterone (7beta,17alpha-dimethyltestosterone) on rat mammary DMBA-induced adenocarcinoma was studied both in vivo and in organ culture. In vivo all 8 tumours with a diameter of less than 30 mm regressed following calusterone injection (10 mg/day for 2-3 weeks). In organ culture calusterone (20 mug/ml medium) inhibited the synthesis of DNA and RNA in all 7 cases examined. Testosterone also inhibited the synthesis of DNA and RNA in organ culture in 12 out of 14 and 10 out of 14 tumours respectively. Oestradiol-17beta on the other hand had no effect on DNA and RNA synthesis in organ culture although 70% of the tumours examined were ovarian dependent, i.e. regressed following castration. This could be explained by the direct effect of calusterone on rat adenocarcinoma compared with the indirect effect of oestradiol-17beta which probably exerts its action by activating the secretion of prolactin which acts on the tumour.
机译:在体内和器官培养中均研究了雌甾酮(7β,17α-二甲基睾丸酮)对大鼠乳腺DMBA诱导的腺癌的作用。体内的所有小于8 mm直径的肿瘤均在注射了卡睾酮后消退(10 mg /天,持续2-3周)。在器官培养中,Calusterone(20杯/毫升培养基)抑制了所检查的所有7例DNA和RNA的合成。睾酮还抑制了14个肿瘤中的12个和14个肿瘤中的10个在器官培养中DNA和RNA的合成。另一方面,Oestradiol-17beta对器官培养物中的DNA和RNA合成没有影响,尽管所检查的肿瘤中有70%是卵巢依赖性的,即去势后已消退。这可能是由于Calusterone对大鼠腺癌的直接作用与oestradiol-17beta的间接作用相比较的,后者可能通过激活作用于肿瘤的催乳激素的分泌发挥作用。

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