Androgen receptors in breast cancer: Expression, value and therapeutic prospects

被引:7
|
作者
Hequet, Delphine [1 ,2 ]
Mzoughi, Slim [1 ]
Rouzier, Roman [2 ,3 ]
Guccione, Ernesto [1 ]
机构
[1] ASTAR, IMCB, Singapour 138673, Singapore
[2] Ctr Rene Huguenin, Inst Curie, Dept Chirurg Oncol, 35 Rue Dailly, F-92210 St Cloud, France
[3] Univ Versailles St Quentin En Yvelines, EA Risques Clin & Securite Sante Femmes & Sante P, 2 Rue Source Bievre, F-78180 Montigny Le Bretonneux, France
关键词
Breast cancer; Androgen receptors; MOLECULAR SUBTYPES; NUCLEAR RECEPTORS; PROSTATE-CANCER; ENZALUTAMIDE; TRANSCRIPTION; CHEMOTHERAPY; BICALUTAMIDE; SENSITIVITY; ENDOCRINE; INHIBITOR;
D O I
10.1016/j.bulcan.2017.01.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple-negative (TN) breast cancer are characterized by lack of estrogen receptor (OR) and progesterone receptor (PR) expression, and the absence of overexpression of human epidermal growth factor receptor 2 (HER2). It is a heterogeneous group of tumors with a more pejorative prognosis than other subtypes of breast cancer. Androgen receptors (AR) are nuclear receptors whose expression varies from 80 to 85% of primary breast cancers and 60 to 75% of metastatic cancers. Among the TN breast cancers, the luminal androgen receptor (LAR) subtype expresses AR more frequently, up to 53% of the cases. AR are associated with lower tumor size, histological grade, Ki67, and lymph node involvement. The results of recent clinical trials evaluating anti-androgen therapies in locally advanced or metastatic TN breast cancer are promising. Many new therapies are tested, including enzalutamide or abiraterone acetate, and numerous therapeutic combinations including PI3K/AKT/mTOR inhibitors or CDK inhibitors. These therapies would allow an alternative treatment of patients with TN breast cancer for which there is often a therapeutic impasse.
引用
收藏
页码:363 / 369
页数:7
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