Katzenellenbogen B S, Tsai T S, Tatee T, Katzenellenbogen J A
Adv Exp Med Biol. 1979;117:111-32. doi: 10.1007/978-1-4757-6589-2_6.
Studies are reported using unlabelled and radiolabelled antiestrogens which are aimed at elucidating the nature of interaction of antiestrogens with uterine and mammary tissue. Antiestrogens and long-acting estrogens move estrogen receptor sites to the nucleus and maintain elevated nuclear receptor levels for a prolonged period. The antagonistic action of antiestrogens in the uterus, however, appears to derive from their ability to effect a marked perturbation in the subcellular distribution of receptor whereby very little (ca. 10%) is cytoplasmic and further estrogen receptor accumulation is blocked. In DMBA-induced rat mammary tumors, the nonphototoxic antiestrogen, U-23, 469, effectively antagonizes the development and growth of tumors and elicits regression of 90% of established tumors with a time course similar to that seen after ovariectomy. Again, during antiestrogen treatment, the levels of cytoplasmic estrogen receptor are depressed with over 90% of total receptor being found in the nucleus. Two radiolabelled antiestrogens of high specific activity and purity have been prepared by us and their interaction with nuclear and cytoplasmic estrogen receptors is reported. Both 3H-CI-628 and 3H-U-23, 469 are metabolized in vivo to more polar forms which are found associated with the nuclear estrogen receptor, and which may be the true agents active in vivo.
有研究报道了使用未标记和放射性标记的抗雌激素药物,旨在阐明抗雌激素与子宫和乳腺组织的相互作用性质。抗雌激素和长效雌激素将雌激素受体位点转移至细胞核,并使细胞核受体水平长时间维持在升高状态。然而,抗雌激素在子宫中的拮抗作用似乎源于它们能够显著扰乱受体的亚细胞分布,使得细胞质中的受体很少(约10%),并且进一步阻止雌激素受体的积累。在二甲基苯并蒽诱导的大鼠乳腺肿瘤中,无光毒性的抗雌激素U-23,469能有效拮抗肿瘤的发生和生长,并使90%已形成的肿瘤消退,其时间进程与卵巢切除术后相似。同样,在抗雌激素治疗期间,细胞质雌激素受体水平降低,超过90%的总受体存在于细胞核中。我们制备了两种高比活性和高纯度的放射性标记抗雌激素,并报道了它们与细胞核和细胞质雌激素受体的相互作用。3H-CI-628和3H-U-23,469在体内均代谢为极性更强的形式,这些形式与细胞核雌激素受体相关,可能是体内真正起作用的物质。