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Craig J Burd
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Lisa M Morey
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Karen E Knudsen
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dissociates from the heat-shock proteins and translocates to the nucleus ( Jenster et al. 1993 , Zhou et al. 1994 ). Active AR homodimers recognize and bind specific DNA sequences called ‘androgen-response elements’ (AREs), which are located in the

Article Type:
Review Article
DOI:
https://doi.org/10.1677/erc.1.01115
Volume/Issue:
Volume 13: Issue 4
Free access
Takuma Uo Department of Medicine, University of Washington, Seattle, Washington, USA

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Stephen R Plymate Department of Medicine, University of Washington, Seattle, Washington, USA
Geriatrics Research Education and Clinical Center, VA Puget Sound Health Care System, Seattle, Washington, USA

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Cynthia C Sprenger Department of Medicine, University of Washington, Seattle, Washington, USA

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ligand-bound AR-FL canonical cistrome, albeit with somewhat weaker ARv567es binding to androgen response elements (AREs) than liganded AR-FL. It should be noted that neither of these studies used AR-V-specific antibodies and although both were done on a

Article Type:
Review Article
DOI:
https://doi.org/10.1530/ERC-17-0108
Volume/Issue:
Volume 24: Issue 9
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Rhonda L Bitting Divisions of Medical Oncology and Urology, Duke Cancer Institute, Duke University, DUMC Box 102002, Durham, North Carolina 27710, USA

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Andrew J Armstrong Divisions of Medical Oncology and Urology, Duke Cancer Institute, Duke University, DUMC Box 102002, Durham, North Carolina 27710, USA

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concentrations achieved during androgen deprivation therapy). Under these conditions, HER2/3 increases binding of the AR to androgen response elements in the promoters of AR target genes and stabilizes the AR protein. To date, however, EGFR and HER

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-12-0394
Volume/Issue:
Volume 20: Issue 3
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Mark P Labrecque Department of Urology, University of Washington School of Medicine, Seattle, Washington, USA

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Joshi J Alumkal Department of Internal Medicine, Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan, USA

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Ilsa M Coleman Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA

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Peter S Nelson Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA
Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA
Department of Medicine, University of Washington School of Medicine, Seattle, Washington, USA

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Colm Morrissey Department of Urology, University of Washington School of Medicine, Seattle, Washington, USA

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-expressing adenocarcinoma specimens with the highest and lowest ARG10 scores were compared to each other in a gene set enrichment analysis (GSEA), the hallmark pathways androgen-response, protein-secretion and oxidative-phosphorylation were the highest pathways present in

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DOI:
https://doi.org/10.1530/ERC-21-0002
Volume/Issue:
Volume 28: Issue 8
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Rayzel C Fernandes Dame Roma Mitchell Cancer Research Laboratories, Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia
Freemasons Foundation Centre for Men’s Health, Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia

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Theresa E Hickey Dame Roma Mitchell Cancer Research Laboratories, Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia

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Wayne D Tilley Dame Roma Mitchell Cancer Research Laboratories, Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia
Freemasons Foundation Centre for Men’s Health, Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia

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Luke A Selth Dame Roma Mitchell Cancer Research Laboratories, Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia
Freemasons Foundation Centre for Men’s Health, Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia

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‘miRNAome’ by binding to androgen response elements (AREs) within cis-regulatory regions that regulate miRNA gene expression ( Fig. 4 ). The integration of AR genome-wide DNA-binding profiles (‘cistromes’) with androgen-regulated transcriptomes has greatly

Article Type:
Review Article
DOI:
https://doi.org/10.1530/ERC-18-0571
Volume/Issue:
Volume 26: Issue 5
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Alba Jiménez-Panizo Department of Biochemistry and Molecular Biomedicine, Institute of Biomedicine (IBUB) of the University of Barcelona (UB), Barcelona, Spain

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Paloma Pérez Instituto de Biomedicina de Valencia (IBV)-CSIC, Valencia, Spain

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Ana M Rojas Computational Biology and Bioinformatics Group, Andalusian Center for Developmental Biology (CABD-CSIC), Sevilla, Spain

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Pablo Fuentes-Prior Molecular Bases of Disease, Biomedical Research Institute Sant Pau (IIB Sant Pau), Barcelona, Spain

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Eva Estébanez-Perpiñá Department of Biochemistry and Molecular Biomedicine, Institute of Biomedicine (IBUB) of the University of Barcelona (UB), Barcelona, Spain

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PL Jivan A Dollins DE Claessens F Gewirth DT 2004 Structural basis of androgen receptor binding to selective androgen response elements . PNAS 101 . ( https://doi.org/10.1073/pnas.0401123101 ) Shen MM Abate-Shen C 2010

Article Type:
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DOI:
https://doi.org/10.1530/ERC-19-0132
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Volume 26: Issue 8
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David A Barron Department of Molecular and Cellular Biology, Baylor College of Medicine, One Baylor Plaza, 325D, mailstop BCM130, Houston, Texas 77030, USA

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David R Rowley Department of Molecular and Cellular Biology, Baylor College of Medicine, One Baylor Plaza, 325D, mailstop BCM130, Houston, Texas 77030, USA

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– 255 . ( doi:10.1002/(SICI)1097-0045(19990901)40:4<248::AID-PROS6>3.0.CO;2-M ). Gerdes MJ Dang TD Larsen M Rowley DR 1998 Transforming growth factor-β1 induces nuclear to cytoplasmic distribution of androgen receptor and inhibits androgen

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-12-0085
Volume/Issue:
Volume 19: Issue 6
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K-M Rau
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H-Y Kang
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T-L Cha
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S A Miller
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M-C Hung
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binding, ER/AR associates with chaperone proteins, heat-shock proteins (Hsps), and the immunophilin complex. After ligand binding, receptors dissociate from chaperone proteins, and form homodimers or heterodimers that can bind to the estrogen- and androgen-response

Article Type:
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DOI:
https://doi.org/10.1677/erc.1.01026
Volume/Issue:
Volume 12: Issue 3
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Salma Kaochar Department of Medicine, Baylor College of Medicine, Houston, Texas, USA
Dan L. Duncan Comprehensive Cancer Center, Houston, Texas, USA
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA

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Aleksandra Rusin Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA

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Christopher Foley Department of Medicine, Baylor College of Medicine, Houston, Texas, USA
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA

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Kimal Rajapakshe Dan L. Duncan Comprehensive Cancer Center, Houston, Texas, USA
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA

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Matthew Robertson Dan L. Duncan Comprehensive Cancer Center, Houston, Texas, USA
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA

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Darlene Skapura Department of Medicine, Baylor College of Medicine, Houston, Texas, USA

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Cammy Mason Department of Medicine, Baylor College of Medicine, Houston, Texas, USA

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Karen Berman De Ruiz Department of Medicine, Baylor College of Medicine, Houston, Texas, USA

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Alexey Mikhailovich Tyryshkin Department of Medicine, Baylor College of Medicine, Houston, Texas, USA

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Jenny Deng Department of Medicine, Baylor College of Medicine, Houston, Texas, USA

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Jin Na Shin Department of Medicine, Baylor College of Medicine, Houston, Texas, USA

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Warren Fiskus Department of Medicine, Baylor College of Medicine, Houston, Texas, USA

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Jianrong Dong Dan L. Duncan Comprehensive Cancer Center, Houston, Texas, USA
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA

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Shixia Huang Dan L. Duncan Comprehensive Cancer Center, Houston, Texas, USA
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA
Department of Education, Innovation, and Technology, Baylor College of Medicine, Houston, Texas, USA

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Nora M Navone Division of Cancer Medicine, Department of Genitourinary Medical Oncology, The University of Texas Anderson Cancer Center, Houston, Texas, USA

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Christel M Davis Avera Institute for Human Genetics, Sioux Falls, South Dakota, USA

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Erik A Ehli Avera Institute for Human Genetics, Sioux Falls, South Dakota, USA

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Cristian Coarfa Dan L. Duncan Comprehensive Cancer Center, Houston, Texas, USA
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA

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Nicholas Mitsiades Department of Medicine, Baylor College of Medicine, Houston, Texas, USA
Dan L. Duncan Comprehensive Cancer Center, Houston, Texas, USA
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA

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Korput HA van Eekelen CC van Rooij HC Faber PW Trapman J 1997 An androgen response element in a far upstream enhancer region is essential for high, androgen-regulated activity of the prostate-specific antigen promoter . Molecular Endocrinology

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-21-0085
Volume/Issue:
Volume 29: Issue 1
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Jennifer Munkley Institute of Genetic Medicine, Newcastle University, Newcastle-upon-Tyne, UK

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. European Urology 66 32 – 39 . ( doi:10.1016/j.eururo.2013.08.011 ) Read JT Rahmani M Boroomand S Allahverdian S McManus BM Rennie PS 2007 Androgen receptor regulation of the versican gene through an androgen response element

Article Type:
Review Article
DOI:
https://doi.org/10.1530/ERC-16-0569
Volume/Issue:
Volume 24: Issue 3
Free access