Antiandrogen ICI 176,334 does not prevent development of androgen insensitivity in S115 mouse mammary tumour cells

Philippa D. Darbre , R.J.B. King
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引用次数: 9

Abstract

Many forms of endocrine therapy for steroid-sensitive tumours involve regimes of steroid agonist deprivation by administration of steroid antagonists. The partial or short-lived response to such therapy results from the inevitable progression of the tumour cells to a state of steroid insensitivity. Several cell culture systems have shown that steroid ablation results in loss of steroid sensitivity and we have used an in vitro model here to study the influence of steroid antagonists on this progression. Growth of androgen-responsive S 115 mouse mammary tumour cells in the long-term absence of steroid results in a loss of androgen-sensitivity. We have studied here the effects of the pure antiandrogen ICI 176,334 on the growth of S 115 cells and on their progression to steroid autonomy. Although a pure antiandrogen in its action on these cells with very low toxicity, it had no protective effect against loss of cellular or molecular androgen-responsive parameters. The clinical implications for endocrine therapy are discussed.

抗雄激素ICI 176,334不能阻止S115小鼠乳腺肿瘤细胞雄激素不敏感的发展
许多形式的内分泌治疗类固醇敏感肿瘤涉及类固醇拮抗剂管理类固醇激动剂剥夺制度。对这种治疗的部分或短暂反应是由于肿瘤细胞不可避免地进展到类固醇不敏感状态。一些细胞培养系统已经表明,类固醇消融导致类固醇敏感性的丧失,我们在这里使用了一个体外模型来研究类固醇拮抗剂对这一进展的影响。在长期缺乏类固醇的情况下,雄激素应答的s115小鼠乳腺肿瘤细胞的生长导致雄激素敏感性的丧失。我们在这里研究了纯抗雄激素ICI 176,334对s115细胞生长及其向类固醇自主发展的影响。虽然纯抗雄激素对这些细胞的作用毒性很低,但它对细胞或分子雄激素反应参数的丧失没有保护作用。讨论了内分泌治疗的临床意义。
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