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
[1]   Tamoxifen-stimulated growth of breast cancer due to p21 loss [J].
Abukhdeir, Abde M. ;
Vitolol, Michele I. ;
Argani, Pedram ;
De Marzo, Angelo M. ;
Karakas, Bedri ;
Konishi, Hiroyuki ;
Gustin, John P. ;
Lauring, Josh ;
Garay, Joseph P. ;
Pendleton, Courtney ;
Konishi, Yuko ;
Blair, Brian G. ;
Brenner, Keith ;
Garrett-Mayer, Elizabeth ;
Carraway, Hetty ;
Bachman, Kurtis E. ;
Park, Ben Ho .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (01) :288-293
[2]   Physiologic estrogen receptor alpha signaling in non-tumorigenic human mammary epithelial cells [J].
Abukhdeir, Abde M. ;
Blair, Brian G. ;
Brenner, Keith ;
Karakas, Bedri ;
Konishi, Hiroyuki ;
Lim, Joselin ;
Sahasranaman, Vanita ;
Huang, Yi ;
Keen, Judith ;
Davidson, Nancy ;
Vitolo, Michele I. ;
Bachman, Kurtis E. ;
Park, Ben Ho .
BREAST CANCER RESEARCH AND TREATMENT, 2006, 99 (01) :23-33
[3]   THE USE OF TESTOSTERONE PROPIONATE IN THE TREATMENT OF ADVANCED CARCINOMA OF THE BREAST [J].
ADAIR, FE ;
HERRMANN, JB .
ANNALS OF SURGERY, 1946, 123 (06) :1023-1035
[4]   Androgen receptor expression in estrogen receptor-negative breast cancer - Immunohistochemical, clinical, and prognostic associations [J].
Agoff, SN ;
Swanson, PE ;
Linden, H ;
Hawes, SE ;
Lawton, TJ .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2003, 120 (05) :725-731
[5]   Conflicting evidence on the frequency of ESR1 amplification in breast cancer [J].
Albertson, Donna G. .
NATURE GENETICS, 2008, 40 (07) :821-822
[6]  
ALLEGRA JC, 1979, CANCER RES, V39, P1447
[7]  
[Anonymous], 1960, JAMA-J AM MED ASSOC, V172, P1271
[8]  
[Anonymous], 1998, LANCET, V351, P1451, DOI DOI 10.1016/S0140-6736(97)11423-4
[9]  
Beatson GT., 1896, LANCET, V148, P104
[10]   Androgen receptor agonist activity of the synthetic progestin, medroxyprogesterone acetate, in human breast cancer cells [J].
Bentel, JM ;
Birrell, SN ;
Pickering, MA ;
Holds, DJ ;
Horsfall, DJ ;
Tilley, WD .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1999, 154 (1-2) :11-20