Androgens and androgen receptors in breast cancer

被引:79
作者
Diaz-Chico, B. Nicolas
German Rodriguez, F.
Gonzalez, Ana
Ramirez, Raquel
Bilbao, Cristina
Cabrera de Leon, A.
Aguirre Jaime, A.
Chirino, Ricardo
Navarro, Domingo
Diaz-Chico, Juan C.
机构
[1] Univ Las Palmas Gran Canaria, Fac Hlth Sci, Dept Biochem & Physiol, Las Palmas Gran Canaria 35080, Canary Islands, Spain
[2] Hosp Univ La Candelaria, Res Unit, Serv Canario Salud, Santa Cruz de Tenerife, Spain
关键词
androgen; androgen receptor; gene polymorphism; breast cancer; carcinogenesis;
D O I
10.1016/j.jsbmb.2006.11.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aromatase (CYP19) converts adrenal and ovarian androgens into estrogens, which supports the growth of estrogen-dependent breast cancers. Anti-aromatase agents are displacing antiestrogens as the first-line treatment for estrogen receptor positive breast cancers. Androgens can act as estrogen precursors, but besides this capability they can also directly act on breast cancer cells by binding to androgen receptors, which are present in the majority of breast cancer specimens. Epidemiological and clinical evidences suggest that higher levels of circulating androgen increase the risk of developing breast cancer. Androgen receptor gene polymorphisms which render the more transcriptionally active receptors have been related to a lower risk of breast cancer. It is currently accepted that androgens act as anti proliferative agents in the presence of estrogens in some breast cancer cell lines. However, emerging evidence suggests that direct androgenic activity might also stimulate cell growth in a subset of estrogen-resistant breast tumors. Here we discuss the supporting evidence which proposes that androgens themselves are actively involved in breast carcinogenesis and its clinical behaviour. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 15
页数:15
相关论文
共 114 条
[1]   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
[2]  
ALLEGRA JC, 1979, CANCER RES, V39, P1447
[3]   Linkage between cryptorchidism, hypospadias, and GGN repeat length in the androgen receptor gene [J].
Aschim, EL ;
Nordenskjöld, A ;
Giwercman, A ;
Lundin, KB ;
Ruhayel, Y ;
Haugen, TB ;
Grotmol, T ;
Giwercman, YL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (10) :5105-5109
[4]   Nuclear hormone receptor co-repressors [J].
Baniahmad, A .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2005, 93 (2-5) :89-97
[5]   Effect of the androgen receptor CAG repeat polymorphism on transcriptional activity: specificity in prostate and non-prostate cell lines [J].
Beilin, J ;
Ball, EMA ;
Favaloro, JM ;
Zajac, JD .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2000, 25 (01) :85-96
[6]   Progress in spinobulbar muscular atrophy research: Insights into neuronal dysfunction caused by the polyglutamine-expanded androgen receptor [J].
Beitel, LK ;
Scanlon, T ;
Gottlieb, B ;
Trifiro, MA .
NEUROTOXICITY RESEARCH, 2005, 7 (03) :219-230
[7]  
BETANCOR E, 2005, 28 ANN SAN ANT BREAS
[8]   Quantitation of androgen receptor gene expression in sporadic breast tumors by real-time RT-PCR:: evidence that MYC is an AR-regulated gene [J].
Bièche, I ;
Parfait, A ;
Tozlu, S ;
Lidereau, R ;
Vidaud, M .
CARCINOGENESIS, 2001, 22 (09) :1521-1526
[9]   Association between androgen receptor gene CAG repeat polymorphism and plasma testosterone levels in postmenopausal women [J].
Brum, IS ;
Spritzer, PM ;
Paris, F ;
Maturana, MA ;
Audran, F ;
Sultan, C .
JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION, 2005, 12 (02) :135-141
[10]   Autonomous driving with concurrent goals and multiple vehicles: Experiments and mobility components [J].
Brumitt, B ;
Stentz, A ;
Hebert, M .
AUTONOMOUS ROBOTS, 2002, 12 (02) :135-156