Sex hormone binding globulin inhibits strongly the uptake of estradiol by human breast carcinoma cells via a deprivative mechanism.

Cancer biochemistry biophysics Pub Date : 1998-10-01
T Zeginiadou, A H Kortsaris, S Koliais, O Antonoglou
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Abstract

A controversy exists for many years about the role of sex hormone binding globulin (SHBG) in the uptake of estradiol by the cells. Using the estradiol-sensitive human breast carcinoma cell line MCF-7 and SHBG isolated from human serum by a new method, we observed a strong inhibition of estradiol uptake. The inhibition was higher when the concentration of the hormone was low. On the other hand, there seemed to be a lag period in inhibition when the concentrations of SHBG were very low, followed by an exponential increase, when the concentration exceeded a critical value. The inhibitory activity was higher when SHBG was added before or along with estradiol in the cell culture, as well as when the incubation period was elongated, while was dramatically minimized by the presence of dihydrotestosterone. Despite the inhibition of estradiol uptake caused by SHBG, the distribution of the hormone in various cell components remained practically the same. In conclusion, all indications from experimental data seem to suggest a simple deprivative mechanism being responsible for the inhibitory activity of SHBG on estradiol uptake by MCF-7 cells in culture.

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性激素结合球蛋白通过剥夺机制强烈抑制人乳腺癌细胞对雌二醇的摄取。
关于性激素结合球蛋白(SHBG)在细胞摄取雌二醇中的作用,多年来一直存在争议。利用从人血清中分离的对雌二醇敏感的人乳腺癌细胞株MCF-7和SHBG,我们观察到它们对雌二醇的摄取有较强的抑制作用。激素浓度越低,抑制作用越强。另一方面,当SHBG浓度很低时,抑制作用似乎有一个滞后期,当浓度超过临界值时,抑制作用呈指数增长。在细胞培养中,在雌二醇之前或同时加入SHBG,以及延长孵育时间时,抑制活性较高,而双氢睾酮的存在显著降低了抑制活性。尽管SHBG抑制了雌二醇的摄取,但激素在各种细胞成分中的分布几乎保持不变。总之,实验数据的所有适应症似乎都表明,SHBG抑制MCF-7细胞对雌二醇摄取的活性有一个简单的剥夺机制。
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