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首页> 外文期刊>The biochemical journal >The metabolism of testosterone and dihydrotestosterone in an androgen-dependent tumour. A possible correlation between dihydrotestosterone and tumour growth in vivo
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The metabolism of testosterone and dihydrotestosterone in an androgen-dependent tumour. A possible correlation between dihydrotestosterone and tumour growth in vivo

机译:雄激素依赖性肿瘤中睾酮和二氢睾酮的代谢。体内二氢睾酮和肿瘤生长之间的可能相关性

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pThe effects of dihydrotestosterone (17β-hydroxy-5α-androstan-3-one) and testosterone on the growth of the androgen-dependent Shionogi SC-115 tumour in mice have been compared and the metabolites in the tumour arising from each steroid have been identified. After the transfer of SC-115 tumour cells to castrated male mice, treatment of the recipients with dihydrotestosterone produced a striking proliferative response that enabled earlier tumour detection and led to a higher tumour incidence than obtained with testosterone. At short intervals after the intravenous injection of 200μCi of [1,2-sup3/supH]testosterone the amounts of radioactivity in tumour, muscle and seminal vesicles were almost equal. The metabolism of [1,2-sup3/supH]testosterone in tumour and muscle was slight in comparison with the extensive metabolism in seminal vesciles. Whereas up to 7% of the total neutral steroid recovered from whole tumour tissue and isolated nuclei was in the form of [1,2-sup3/supH]dihydrotestosterone, the amount of this compound in the corresponding preparations from seminal vesciles was several times greater. When the metabolism of [1,2-sup3/supH]dihydrotestosterone in tumour tissue was studied, it was found that more than 60% of the total neutral steroid in both cytoplasm and nuclei consisted of [1,2-sup3/supH]dihydrotestosterone. Thus much higher intracellular concentrations of dihydrotestosterone occurred with the administration of this steroid than with testosterone. Tumour cell proliferation was suppressed by oestradiol and the amount of androgen in nuclei was significantly decreased by high doses of this hormone./p
机译:[p>已经比较了二氢酮(17β-羟基-5α-甾烷-3-一)和睾酮对小鼠雄激素依赖性SC-115肿瘤生长的影响,并且每个类固醇引起的肿瘤中的代谢物已被确定。转移SC-115肿瘤细胞以阉割的雄性小鼠后,用DioHolotestorone治疗接受者产生的引人注目的增殖反应,使得最早的肿瘤检测能够导致肿瘤发病率比睾酮所获得的肿瘤发生率。在静脉注射200μCI的[1,2- 3 h]睾酮后,肿瘤,肌肉和精髓囊泡的量几乎相等,几乎相等。肿瘤和肌肉中的[1,2- 3 h]睾酮的代谢与初始vesciles中的广泛代谢相比,肿瘤和肌肉呈显着。虽然从整个肿瘤组织和分离的核中回收的最多7%的总中性类固醇是[1,2- 3 h]二氢睾酮的形式,相应制剂中的该化合物的量精英vesciles几倍多。当研究肿瘤组织中[1,2- 3 h]二氢睾酮的代谢时,发现两种细胞质和核中的总中性类固醇中的超过60%包括[1,2 - 3 h] dihydrottosterone。因此,施用该类固醇的细胞内细胞内浓度高于睾酮。通过Ostrodiol抑制肿瘤细胞增殖,并且通过该激素的高剂量核抑制核中的雄激素量显着降低。

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