Suzuki N, Wakisaka M, Miyauchi T, Shimazaki J, Hosoya T
Endocrinol Jpn. 1983 Feb;30(1):15-21. doi: 10.1507/endocrj1954.30.15.
To observe the effect of sex hormones on RNA synthesis of androgen-dependent tumors, mice of DD/S strain bearing androgen-dependent mouse mammary tumor (SC 115) were treated with the hormones, and RNA polymerase activities in isolated nuclei of the tumor were measured. The activity of RNA polymerase I in SC 115 was diminished to approximately 60% of the control level by castration, and it was restored to the precastrated level 12 hr after treatment with 0.2 mg of testosterone. While the activity of RNA polymerase II in the tumor was scarcely influenced by castration, it reached 150% of the castrated level 24 hr after administration of testosterone. In CS 1, a subline of SC 115 with partial loss of androgen dependency on growth, castration and testosterone treatment caused similar but less prominent effects on the activities of RNA polymerase. Administration of estradiol-17 beta to castrated animals also increased the activity of RNA polymerase I, but to a lesser degree than testosterone, in both SC 115 and CS 1. However, only SC 115 demonstrated an increase in RNA polymerase II after estrogen treatment.
为观察性激素对雄激素依赖性肿瘤RNA合成的影响,用性激素处理携带雄激素依赖性小鼠乳腺肿瘤(SC 115)的DD/S品系小鼠,并测定肿瘤分离细胞核中的RNA聚合酶活性。去势后,SC 115中RNA聚合酶I的活性降至对照水平的约60%,用0.2 mg睾酮处理12小时后恢复到去势前水平。虽然肿瘤中RNA聚合酶II的活性几乎不受去势影响,但在给予睾酮24小时后,其活性达到去势水平的150%。在SC 115的一个亚系CS 1中,其生长对雄激素的依赖性部分丧失,去势和睾酮处理对RNA聚合酶活性产生类似但不太明显的影响。在SC 115和CS 1中,给去势动物注射17β-雌二醇也会增加RNA聚合酶I的活性,但程度低于睾酮。然而,只有SC 115在雌激素处理后RNA聚合酶II活性增加。