Dowsett M, Howell R, Salter J, Thomas N M, Thomas E J
Academic Department of Biochemistry, Royal Marsden Hospital, London, UK
Hum Reprod. 1995 Feb;10(2):262-7. doi: 10.1093/oxfordjournals.humrep.a135926.
The new steroidal pure anti-oestrogen ICI 182780 was studied for the first time in pre-menopausal women. A total of 30 patients requiring hysterectomy for benign gynaecological disease were randomized to ICI 182780, 12 mg/day i.m. (n = 19) or no treatment (n = 11) for 7 days prior to surgery. Immunohistochemical measurements were made in the snap-frozen, resected endometrium for oestrogen receptors (ER), progesterone receptors (PgR) and Ki67, a nuclear antigen whose expression is closely related to proliferation. Five control patients ovulated prior to surgery and, as expected, the secretory endometria had lower Ki67 antigen concentrations than endometria had lower proliferative phase. The endometria from patients treated with ICI 182780 had reduced Ki67 compared with controls. This demonstration of reduced proliferative activity indicates that the pharmacological effectiveness of the treatment was maintained despite increased plasma oestradiol concentrations. In contrast to results from rodents, ICI 182780 did not markedly reduce ER expression, although there was significantly lower ER in the myometrial cells of the treated group. The lack of effect on PgR shows a dissociation between the drug's effect on this oestrogen-dependent protein and its effects on proliferation.
新型甾体类纯抗雌激素药物ICI 182780首次在绝经前女性中进行研究。共有30例因良性妇科疾病需要进行子宫切除术的患者被随机分为两组,一组接受ICI 182780治疗,剂量为12毫克/天,肌肉注射(n = 19),另一组不接受治疗(n = 11),在手术前7天给药。对手术切除的子宫内膜进行速冻处理后,通过免疫组织化学方法检测雌激素受体(ER)、孕激素受体(PgR)以及Ki67,Ki67是一种核抗原,其表达与细胞增殖密切相关。5例对照患者在手术前排卵,正如预期的那样,分泌期子宫内膜的Ki67抗原浓度低于增殖期子宫内膜。与对照组相比,接受ICI 182780治疗患者的子宫内膜Ki67表达降低。增殖活性降低表明,尽管血浆雌二醇浓度升高,但该治疗的药理效果得以维持。与啮齿动物实验结果相反,ICI 182780并未显著降低ER表达,尽管治疗组子宫肌层细胞中的ER显著减少。对PgR无影响表明,该药物对这种雌激素依赖性蛋白的作用与其对增殖的作用之间存在分离。