Mehta R G, Cerny W L, Moon R C
Oncology. 1984;41(6):387-92. doi: 10.1159/000225860.
Recently, several investigators have demonstrated the presence of triphenylethylene antiestrogen binding sites in the cytoplasm of many tissues, which specifically bind to radioactive tamoxifen with high affinity. Although mammary gland is one of the principal target organs for antiestrogen action, the characterization of antiestrogen binding in mammary tissues has not been reported. We have studied the antiestrogen binding properties of [3H]tamoxifen in the mammary glands of virgin, pregnant and lactating rats as well as in the N-methyl-N-nitrosourea-induced mammary tumors. Tritium labeled tamoxifen bound specifically and with high affinity (Kd = 10(-9) M) to components present in 25,000 g supernatant. Unlabeled estradiol or DES did not compete for these sites, whereas unlabeled tamoxifen showed competitive inhibition. The mammary glands contained threefold higher levels of cytoplasmic binding sites as compared to the mammary tumors. Mammary glands from the pregnant rats bound tamoxifen to a greater extent than that of either virgin or lactating rats. The functional relevance of these binding sites is still unknown.
最近,几位研究人员已证实在许多组织的细胞质中存在三苯乙烯抗雌激素结合位点,这些位点能以高亲和力特异性结合放射性他莫昔芬。尽管乳腺是抗雌激素作用的主要靶器官之一,但尚未见有关乳腺组织中抗雌激素结合特性的报道。我们研究了[3H]他莫昔芬在未孕、妊娠和哺乳期大鼠乳腺以及N-甲基-N-亚硝基脲诱导的乳腺肿瘤中的抗雌激素结合特性。氚标记的他莫昔芬与25,000g上清液中的成分特异性结合且亲和力高(解离常数Kd = 10^(-9)M)。未标记的雌二醇或己烯雌酚不竞争这些位点,而未标记的他莫昔芬表现出竞争性抑制。与乳腺肿瘤相比,乳腺组织中的细胞质结合位点水平高三倍。妊娠大鼠的乳腺比未孕或哺乳期大鼠的乳腺结合他莫昔芬的程度更高。这些结合位点的功能相关性仍不清楚。