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雌激素对乳腺癌风险的矛盾临床效应:雌激素诱导细胞凋亡的“新”生物学。

Paradoxical clinical effect of estrogen on breast cancer risk: a "new" biology of estrogen-induced apoptosis.

机构信息

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USA.

出版信息

Cancer Prev Res (Phila). 2011 May;4(5):633-7. doi: 10.1158/1940-6207.CAPR-11-0185. Epub 2011 Apr 10.

Abstract

Administration of estrogen replacement therapy (ERT) decreases the incidence of breast cancer, as shown in a double-blind, placebo-controlled randomized trial of the Women's Health Initiative (WHI) in 10,739 postmenopausal women with a prior hysterectomy. Although paradoxical because estrogen is recognized to stimulate breast cancer growth, laboratory data support a mechanism of estrogen-induced apoptosis under the correct environmental circumstances. Long-term antiestrogen treatment or estrogen deprivation causes the eventual development and evolution of antihormone resistance. Cell populations emerge with a vulnerability, as estrogen is no longer a survival signal but is an apoptotic trigger. The antitumor effect of ERT in estrogen-deprived postmenopausal women is consistent with laboratory models.

摘要

雌激素替代疗法(ERT)的管理可降低乳腺癌的发生率,这在一项针对 10739 名有子宫切除术史的绝经后妇女的妇女健康倡议(WHI)的双盲、安慰剂对照随机试验中得到了证实。尽管雌激素被认为会刺激乳腺癌生长,这似乎有些矛盾,但实验室数据支持在正确的环境条件下,雌激素诱导细胞凋亡的机制。长期的抗雌激素治疗或雌激素剥夺会导致最终产生抗激素耐药性。当雌激素不再是生存信号而是凋亡触发因素时,细胞群体就会出现易损性。ERT 在雌激素剥夺的绝经后妇女中的抗肿瘤作用与实验室模型一致。

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