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作 者:卢建[1] 张金山[1] 曾燕[1] 牟翰舟 许沈华
出 处:《中华妇产科杂志》1995年第6期360-362,共3页Chinese Journal of Obstetrics and Gynecology
摘 要:以人工合成的雄激素[17α-甲基 ̄3H]-三烯醇酮( ̄3H-R1881)为配体,采用完整细胞受体测定法,测定人卵巢癌HO-8910细胞的雄激素受体(AR),并观察不同浓度(0.01~1μmol/L)的雌二醇、孕酮及睾酮对HO-8910细胞增殖的影响。结果:HO-8910细胞具有高亲和力、低容量的雄激素特异结合位点,用Scatchard分析法求得其最大结合容量(Ro)及表观解离常数(Kd)分别为6.52fmol/10 ̄6细胞及2.96nmol/L。表明:HO-8910细胞存在AR。经上述性激素作用后,HO-8910细胞的增殖率没有明显的变化,表明性激素对该细胞的增殖无明显影响。revious study had showed that ovarian carcinoma cell line (HO-8910 cells) contained estrogen re-ceptors(ER)and progesterone receptors(PR). In this experiment,androgen receptors(AR)in these cells were determined by a whole cell binding assay with a synthetic nonmetabolizable androgen-methyl-trienolone( ̄3H-R1881).The results showed that there existed high affinity and low capacity, specific binding sites for  ̄3H-R1881 in these cells,the apparent maximum binding capacity and dissociation con-stant of these bindings sites revealed by scathchard analysis being 6. 52 fmol/10 ̄6 cells and 2. 96 nmol/L respectively,indicating the presence of AR in addition to ER and PR in HO-8910 cells. Furthermore,the effects of sex hOrmones,i.e., estrodiol, progesterone and testosterone on the growth of HO-8910 cells were also investigated. The results showed that testosterone at 10 nmol/L slightly increased the number of HO-8910 cells,but the increase was not dose-dependent and not statistically significant. Es-trodiol and progesterone had no growth-stimulatary or inhibitary effects on these cells.
分 类 号:R737.310.2[医药卫生—肿瘤]
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