Molecular biology of the androgen receptor: From molecular understanding to the clinic

被引:98
作者
Eder, IE [1 ]
Culig, Z [1 ]
Putz, T [1 ]
Nessler-Menardi, C [1 ]
Bartsch, G [1 ]
Klocker, H [1 ]
机构
[1] Univ Innsbruck, Dept Urol, A-6020 Innsbruck, Austria
关键词
androgen receptor; androgen insensitivity; mutations; prostate cancer; therapy;
D O I
10.1159/000049782
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The androgen receptor (AR) is the key regulatory element of androgen signaling in the cell. It mediates action of androgens and is therefore essential for growth, function and differentiation of the human male urogenital tract. Genetic alterations in the AR gene may cause impaired development resulting in androgen insensitivity syndromes (AIS) or in neurodegenerative diseases like Kennedy syndrome. Besides the crucial role in the process of virilization during embryogenesis and puberty, the AR also plays an important role in the adult man as the intracellular mediator of androgen action. Androgen withdrawal and/or AR blockade is the main choice of treatment of nonorgan-confined prostate cancer. Unfortunately, this treatment is only palliative and a majority of these tumors recur and progress to an androgen-independent and therapy-resistant stage. Recent findings gave new insight into the molecular structure and function of the AR and improved our understanding about prostate cancer progression, consequently resulting in the development of novel treatments. It has become evident that the AR is a nuclear transcription factor that can be activated ligand-dependently by androgens as well as ligand-independently by other hormones and various growth factors, respectively. Moreover, it was shown that the interaction of the AR with other proteins of the intracellular signal transduction cascade may promote prostate tumor growth, This review will summarize the most important findings about the AR and the androgen signaling pathway to improve the understanding of prostate diseases and novel treatment strategies that may be useful in the clinic. Copyright (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:241 / 251
页数:11
相关论文
共 126 条
[1]   ANDROGEN-SPECIFIC GENE ACTIVATION VIA A CONSENSUS GLUCOCORTICOID RESPONSE ELEMENT IS DETERMINED BY INTERACTION WITH NONRECEPTOR FACTORS [J].
ADLER, AJ ;
DANIELSEN, M ;
ROBINS, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (24) :11660-11663
[2]   Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome [J].
Ahmed, SF ;
Cheng, A ;
Dovey, L ;
Hawkins, JR ;
Martin, H ;
Rowland, J ;
Shimura, N ;
Tait, AD ;
Hughes, IA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (02) :658-665
[3]   Interaction of the putative androgen receptor-specific coactivator ARA70/ELE1α with multiple steroid receptors and identification of an internally deleted ELE1β isoform [J].
Alen, P ;
Claessens, F ;
Schoenmakers, E ;
Swinnen, JV ;
Verhoeven, G ;
Rombauts, W ;
Peeters, B .
MOLECULAR ENDOCRINOLOGY, 1999, 13 (01) :117-128
[4]   A FAMILY WITH ADULT SPINAL AND BULBAR MUSCULAR-ATROPHY, X-LINKED INHERITANCE AND ASSOCIATED TESTICULAR FAILURE [J].
ARBIZU, T ;
SANTAMARIA, J ;
GOMEZ, JM ;
QUILEZ, A ;
SERRA, JP .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1983, 59 (03) :371-382
[5]   Functional interactions of the AF-2 activation domain core region of the human androgen receptor with the amino-terminal domain and with the transcriptional coactivator TIF2 (transcriptional intermediary factor 2) [J].
Berrevoets, CA ;
Doesburg, P ;
Steketee, K ;
Trapman, J ;
Brinkmann, AO .
MOLECULAR ENDOCRINOLOGY, 1998, 12 (08) :1172-1183
[6]   COMBINING PROSTATE-SPECIFIC ANTIGEN WITH CANCER AND GLAND VOLUME TO PREDICT MORE RELIABLY PATHOLOGICAL STAGE - THE INFLUENCE OF PROSTATE-SPECIFIC ANTIGEN CANCER DENSITY [J].
BLACKWELL, KL ;
BOSTWICK, DG ;
MYERS, RP ;
ZINCKE, H ;
OESTERLING, JE .
JOURNAL OF UROLOGY, 1994, 151 (06) :1565-1570
[7]   Forskolin-induced dephosphorylation of the androgen receptor impairs ligand binding [J].
Blok, LJ ;
de Ruiter, PE ;
Brinkmann, AO .
BIOCHEMISTRY, 1998, 37 (11) :3850-3857
[8]   Androgen receptor phosphorylation [J].
Blok, LJ ;
deRuiter, PE ;
Brinkmann, AO .
ENDOCRINE RESEARCH, 1996, 22 (03) :197-219
[9]   CAG repeat length in the androgen receptor gene is related to age at diagnosis of prostate cancer and response to endocrine therapy, but not to prostate cancer risk [J].
Bratt, O ;
Borg, Å ;
Kristoffersson, U ;
Lundgren, R ;
Zhang, QX ;
Olsson, H .
BRITISH JOURNAL OF CANCER, 1999, 81 (04) :672-676
[10]   THE HUMAN ANDROGEN RECEPTOR - STRUCTURE-FUNCTION RELATIONSHIP IN NORMAL AND PATHOLOGICAL SITUATIONS [J].
BRINKMANN, AO ;
JENSTER, G ;
KUIPER, GGJM ;
RIS, C ;
VANLAAR, JH ;
VANDERKORPUT, JAGM ;
DEGENHART, HJ ;
TRIFIRO, MA ;
PINSKY, L ;
ROMALO, G ;
SCHWEIKERT, HU ;
VELDSCHOLTE, J ;
MULDER, E ;
TRAPMAN, J .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 41 (3-8) :361-368