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
相关论文
共 47 条
[11]  
Chun-Wei Wang, 2016, Sensing and Bio-Sensing Research, V7, P7, DOI 10.1016/j.sbsr.2015.11.002
[12]   PD 0332991, a selective cyclin D kinase 4/6 inhibitor, preferentially inhibits proliferation of luminal estrogen receptor-positive human breast cancer cell lines in vitro [J].
Finn, Richard S. ;
Dering, Judy ;
Conklin, Dylan ;
Kalous, Ondrej ;
Cohen, David J. ;
Desai, Amrita J. ;
Ginther, Charles ;
Atefi, Mohammad ;
Chen, Isan ;
Fowst, Camilla ;
Los, Gerret ;
Slamon, Dennis J. .
BREAST CANCER RESEARCH, 2009, 11 (05)
[13]   Molecular taxonomy of luminal breast cancer in 2015 [J].
Franchet, Camille ;
Duprez-Paumier, Raphaelle ;
Lacroix-Triki, Magali .
BULLETIN DU CANCER, 2015, 102 (06) :S34-S46
[14]   Strategies for subtypes-dealing with the diversity of breast cancer: highlights of the St Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2011 [J].
Goldhirsch, A. ;
Wood, W. C. ;
Coates, A. S. ;
Gelber, R. D. ;
Thuerlimann, B. ;
Senn, H. -J. .
ANNALS OF ONCOLOGY, 2011, 22 (08) :1736-1747
[15]   Phase II Trial of Bicalutamide in Patients with Androgen Receptor-Positive, Estrogen Receptor-Negative Metastatic Breast Cancer [J].
Gucalp, Ayca ;
Tolaney, Sara ;
Isakoff, Steven J. ;
Ingle, James N. ;
Liu, Minetta C. ;
Carey, Lisa A. ;
Blackwell, Kimberly ;
Rugo, Hope ;
Nabell, Lisle ;
Forero, Andres ;
Stearns, Vered ;
Doane, Ashley S. ;
Danso, Michael ;
Moynahan, Mary Ellen ;
Momen, Lamia F. ;
Gonzalez, Joseph M. ;
Akhtar, Arooj ;
Giri, Dilip D. ;
Patil, Sujata ;
Feigin, Kimberly N. ;
Hudis, Clifford A. ;
Traina, Tiffany A. .
CLINICAL CANCER RESEARCH, 2013, 19 (19) :5505-5512
[16]   Expression of androgen receptor splice variants in clinical breast cancers [J].
Hickey, Theresa E. ;
Irvine, Connie M. ;
Dvinge, Heidi ;
Tarulli, Gerard A. ;
Hanson, Adrienne R. ;
Ryan, Natalie K. ;
Pickering, Marie A. ;
Birrell, Stephen N. ;
Hu, Dong Gui ;
Mackenzie, Peter I. ;
Russell, Roslin ;
Caldas, Carlos ;
Raj, Ganesh V. ;
Dehm, Scott M. ;
Plymate, Stephen R. ;
Bradley, Robert K. ;
Tilley, Wayne D. ;
Selth, Luke A. .
ONCOTARGET, 2015, 6 (42) :44728-44744
[17]   Clinical importance of estrogen receptor-β evaluation in breast cancer patients treated with adjuvant tamoxifen therapy [J].
Honma, Naoko ;
Horii, Rie ;
Iwase, Takuji ;
Saji, Shigehira ;
Younes, Mamoun ;
Takubo, Kaiyo ;
Matsuura, Masaaki ;
Ito, Yoshinori ;
Akiyama, Futoshi ;
Sakamoto, Goi .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (22) :3727-3734
[18]   Androgen Receptor Expression and Breast Cancer Survival in Postmenopausal Women [J].
Hu, Rong ;
Dawood, Shaheenah ;
Holmes, Michelle D. ;
Collins, Laura C. ;
Schnitt, Stuart J. ;
Cole, Kimberley ;
Marotti, Jonathan D. ;
Hankinson, Susan E. ;
Colditz, Graham A. ;
Tamimi, Rulla M. .
CLINICAL CANCER RESEARCH, 2011, 17 (07) :1867-1874
[19]   Androgen-Responsive Gene Database: Integrated Knowledge on Androgen-Responsive Genes [J].
Jiang, Mei ;
Ma, Yunsheng ;
Chen, Congcong ;
Fu, Xuping ;
Yang, Shu ;
Li, Xia ;
Yu, Guohua ;
Mao, Yumin ;
Xie, Yi ;
Li, Yao .
MOLECULAR ENDOCRINOLOGY, 2009, 23 (11) :1927-1933
[20]   Cooperativity and equilibrium with FOXA1 define the androgen receptor transcriptional program [J].
Jin, Hong-Jian ;
Zhao, Jonathan C. ;
Wu, Longtao ;
Kim, Jung ;
Yu, Jindan .
NATURE COMMUNICATIONS, 2014, 5