Androgen receptor as a targeted therapy for breast cancer

被引:1
作者
Garay, Joseph P. [1 ]
Park, Ben H. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Sch Med, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Whiting Sch Engn, Dept Chem & Biomol Engn, Baltimore, MD 21231 USA
关键词
Androgen receptor; MAP kinase; breast cancer; p21; androgens;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer occurs at a high frequency in women and, given this fact, a primary focus of breast cancer research has been the study of estrogen receptor alpha (ER) signaling. However, androgens are known to play a role in normal breast physiology and therefore androgen receptor (AR) signaling is becoming increasingly recognized as an important contributor towards breast carcinogenesis. Moreover, the high frequency of AR expression in breast cancer makes it an attractive therapeutic target, but the ability to exploit AR for therapy has been difficult. Here we review the historical use of androgen/anti-androgen therapies in breast cancer, the challenges of accurately modeling nuclear hormone receptor signaling in vitro, and the presence and prognostic significance of AR in breast cancer.
引用
收藏
页码:434 / 445
页数:12
相关论文
共 90 条
[71]   Estrogen-dependent cyclin E-cdk2 activation through p21 redistribution [J].
PlanasSilva, MD ;
Weinberg, RA .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (07) :4059-4069
[72]   ANDROGEN AND GLUCOCORTICOID RECEPTOR-MEDIATED INHIBITION OF CELL-PROLIFERATION BY MEDROXYPROGESTERONE ACETATE IN ZR-75-1 HUMAN-BREAST CANCER-CELLS [J].
POULIN, R ;
BAKER, D ;
POIRIER, D ;
LABRIE, F .
BREAST CANCER RESEARCH AND TREATMENT, 1989, 13 (02) :161-172
[73]   ANDROGENS INHIBIT BASAL AND ESTROGEN-INDUCED CELL-PROLIFERATION IN THE ZR-75-1 HUMAN-BREAST CANCER CELL-LINE [J].
POULIN, R ;
BAKER, D ;
LABRIE, F .
BREAST CANCER RESEARCH AND TREATMENT, 1988, 12 (02) :213-225
[74]   Prognostic markers in triple-negative breast cancer [J].
Rakha, Emad A. ;
El-Sayed, Maysa E. ;
Green, Andrew R. ;
Lee, Andrew H. S. ;
Robertson, John F. ;
Ellis, Ian O. .
CANCER, 2007, 109 (01) :25-32
[75]   Modification of BRCA1-associated breast cancer risk by the polymorphic androgen-receptor CAG repeat [J].
Rebbeck, TR ;
Kantoff, PN ;
Krithivas, K ;
Neuhausen, S ;
Blackwood, MA ;
Godwin, AK ;
Daly, MB ;
Narod, SA ;
Garber, JE ;
Lynch, HT ;
Weber, BL ;
Brown, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (05) :1371-1377
[76]  
REESE CC, 1988, ANN NY ACAD SCI, V538, P112
[77]   ESR1 gene amplification in breast cancer: a common phenomenon? [J].
Jorge S Reis-Filho ;
Suzanne Drury ;
Maryou B Lambros ;
Caterina Marchio ;
Nichola Johnson ;
Rachael Natrajan ;
Janine Salter ;
Pauline Levey ;
Olivia Fletcher ;
Julian Peto ;
Alan Ashworth ;
Mitch Dowsett .
Nature Genetics, 2008, 40 (7) :809-810
[78]   Association of kallikrein expression in nipple aspirate fluid with breast cancer risk [J].
Sauter, ER ;
Lininger, J ;
Magklara, A ;
Hewett, JE ;
Diamandis, EP .
INTERNATIONAL JOURNAL OF CANCER, 2004, 108 (04) :588-591
[79]   Evaluation of the prognostic significance of androgen receptor expression in metastatic breast cancer [J].
Schippinger, W ;
Regitnig, P ;
Dandachi, N ;
Wernecke, KD ;
Bauernhofer, T ;
Samonigg, H ;
Moinfar, F .
VIRCHOWS ARCHIV, 2006, 449 (01) :24-30
[80]   Breast Tumor Cells with PI3K Mutation or HER2 Amplification Are Selectively Addicted to Akt Signaling [J].
She, Qing-Bai ;
Chandarlapaty, Sarat ;
Ye, Qing ;
Lobo, Jose ;
Haskell, Kathleen M. ;
Leander, Karen R. ;
DeFeo-Jones, Deborah ;
Huber, Hans E. ;
Rosen, Neal .
PLOS ONE, 2008, 3 (08)