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1. Full Text Compartmentalization of Androgen Receptor Protein-Protein Interactions in Living Cells
by Martin E. van Royen and Sónia M. Cunha and Maartje C. Brink and Karin A. Mattern and Alex L. Nigg and Hendrikus J. Dubbink and Pernette J. Verschure and Jan Trapman and Adriaan B. Houtsmuller
The Journal of Cell Biology, ISSN 0021-9525, 4/2007, Volume 177, Issue 1, pp. 63 - 72
Steroid receptors regulate gene expression in a ligand-dependent manner by binding specific DNA sequences. Ligand binding also changes the conformation of the... 
Ratios | Androgen receptors | Imaging | Cell nucleus | DNA | Cell lines | Fluorescence | Ligands | Pixels | Nuclear interactions | RNA-POLYMERASE-II | DNA-BINDING | COACTIVATOR | ACTIVATION | GLUCOCORTICOID-RECEPTOR | IN-VIVO | TRANSCRIPTION | SITES | LIGAND-BINDING DOMAIN | PROGESTERONE-RECEPTOR | CELL BIOLOGY | Cell Line | Fluorescence Recovery After Photobleaching | Humans | Receptors, Androgen - metabolism | Recombinant Fusion Proteins - analysis | Intracellular Signaling Peptides and Proteins - metabolism | DNA - metabolism | Amino Acid Motifs | Protein Interaction Mapping | Luminescent Proteins - analysis | Receptors, Androgen - analysis | Fluorescence Resonance Energy Transfer | Receptors, Androgen - chemistry | Binding Sites
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2. Full Text Interference with the androgen receptor protein stability in therapy‐resistant prostate cancer
by Lakshmana, Gopinath and Baniahmad, Aria
International Journal of Cancer, ISSN 0020-7136, 04/2019, Volume 144, Issue 8, pp. 1775 - 1779
The androgen receptor (AR) plays a central role in the pathogenesis of prostate cancer (PCa). Most PCa cases develop eventually from an androgen‐dependent... 
receptor degradation | castration resistance | androgen receptor | protein stability | therapy resistance | CELLS | AR-V7 | SPLICE VARIANT | OPEN-LABEL | GANETESPIB | MECHANISMS | CONFERS RESISTANCE | GLUCOCORTICOID-RECEPTOR | ONCOLOGY | INHIBITOR | Receptors, Glucocorticoid - antagonists & inhibitors | Androgen Receptor Antagonists - therapeutic use | Heat-Shock Proteins - metabolism | Humans | Receptors, Androgen - metabolism | Ubiquitin-Protein Ligases - metabolism | Ubiquitin-Protein Ligases - antagonists & inhibitors | Heat-Shock Proteins - antagonists & inhibitors | Male | Antineoplastic Agents - therapeutic use | Receptors, Glucocorticoid - metabolism | Prostatic Neoplasms, Castration-Resistant - drug therapy | Androgen Receptor Antagonists - pharmacology | Prostatic Neoplasms, Castration-Resistant - pathology | Prostate - pathology | Proteolysis - drug effects | Signal Transduction - drug effects | Protein Stability - drug effects | Treatment Failure | Prostate - drug effects | Antineoplastic Agents - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | Drug Resistance, Neoplasm - drug effects | Proteins | Care and treatment | Prostate cancer | Health aspects | Cancer | Therapy | Stability | Glucocorticoids | Therapeutic applications | Pathogenesis | Heat shock proteins | Chaperones | Carcinogenesis | Signaling | Carcinogens | Androgens | Molecular modelling | Castration | Evolution | Prostate | Heat shock | Index Medicus
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3. Full Text Clinical Significance of Epidermal Growth Factor Receptor Protein Overexpression and Gene Copy Number Gains in Prostate Cancer
by Thorsten Schlomm and Patrick Kirstein and Liv Iwers and Birte Daniel and Thomas Steuber and Jochen Walz and Felix H.K. Chun and Alexander Haese and Jens Kollermann and Markus Graefen and Hartwig Huland and Guido Sauter and Ronald Simon and Andreas Erbersdobler
Clinical Cancer Research, ISSN 1078-0432, 11/2007, Volume 13, Issue 22, pp. 6579 - 6584
Purpose: The epidermal growth factor receptor (EGFR) is a protein involved in the tumor progression of many cancer types and is an important therapeutic... 
Immunohistochemistry | Gene amplification | Targeted therapy | EGFR | Genitourinary cancers: prostate | CELL LUNG-CANCER | ONCOLOGY | CARCINOMAS | IN-SITU-HYBRIDIZATION | MICROARRAYS | MUTATIONS | GEFITINIB SENSITIVITY | ANDROGEN-INDEPENDENCE | EXPRESSION | PROGRESSION | Prostatic Neoplasms - pathology | Receptor, Epidermal Growth Factor - genetics | Up-Regulation | Prognosis | Humans | Middle Aged | In Situ Hybridization, Fluorescence | Male | Gene Dosage | Receptor, Epidermal Growth Factor - analysis | Prostatic Neoplasms - diagnosis | Receptor, Epidermal Growth Factor - metabolism | Prostatic Neoplasms - enzymology | Aged | DNA, Neoplasm - analysis | Mutation
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4. Full Text Cepharanthine hydrochloride degrades polyglutamine-expanded androgen receptor proteins through an autophagy pathway in neuron cells
by Wang, Yao and Wang, Yifei and Su, Guifeng and Huang, Zexiu and Fan, Jianglin
European Journal of Pharmacology, ISSN 0014-2999, 10/2019, Volume 861, p. 172534
Cepharanthine is a biscoclaurine alkaloid extracted from that has a variety of biological activities in multiple diseases. Spinal and bulbar muscular atrophy... 
Degradation | Spinal and bulbar muscular atrophy | Cepharanthine hydrochloride | Polyglutamine | Autophagy | Androgen receptor | SHOCK | DISEASE | PHARMACOLOGY & PHARMACY | CANCER
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5. Full Text CHIP Overexpression Reduces Mutant Androgen Receptor Protein and Ameliorates Phenotypes of the Spinal and Bulbar Muscular Atrophy Transgenic Mouse Model
by Adachi, Hiroaki and Waza, Masahiro and Tokui, Keisuke and Katsuno, Masahisa and Minamiyama, Makoto and Tanaka, Fumiaki and Doyu, Manabu and Sobue, Gen
Journal of Neuroscience, ISSN 0270-6474, 05/2007, Volume 27, Issue 19, pp. 5115 - 5126
Spinal and bulbar muscular atrophy (SBMA) is an inherited motor neuron disease caused by the expansion of a polyglutamine tract within the androgen receptor... 
Protein degradation | CHIP | Polyglutamine | SBMA | Androgen receptor | Transgenic mice | LIGASE CHIP | MOLECULAR CHAPERONES | RECESSIVE BULBOSPINAL NEURONOPATHY | QUALITY-CONTROL | polyglutamine | 70-INTERACTING PROTEIN | NEUROSCIENCES | E3 LIGASE | HEAT-SHOCK PROTEINS | androgen receptor | transgenic mice | CO-CHAPERONE CHIP | CARBOXYL-TERMINUS | protein degradation | UBIQUITIN-PROTEASOME PATHWAY | Central Nervous System - metabolism | Humans | Receptors, Androgen - metabolism | Nerve Degeneration - genetics | Male | Motor Neurons - pathology | Nerve Degeneration - metabolism | Muscular Atrophy, Spinal - genetics | Female | Inclusion Bodies - metabolism | Disease Models, Animal | Genetic Predisposition to Disease - genetics | Muscular Atrophy, Spinal - metabolism | Heat-Shock Proteins - metabolism | Intranuclear Inclusion Bodies - genetics | Gene Expression Regulation - physiology | Mice, Transgenic | Mutation - genetics | Down-Regulation - genetics | Protein Folding | Motor Neurons - metabolism | Inclusion Bodies - genetics | Phenotype | Animals | Receptors, Androgen - genetics | Muscular Atrophy, Spinal - therapy | Mice | Central Nervous System - physiopathology | Proteasome Endopeptidase Complex - metabolism | Ubiquitin-Protein Ligases - genetics | Intranuclear Inclusion Bodies - metabolism | Genetic Therapy - methods | Nerve Degeneration - therapy
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6. Full Text Coupling of conformational transitions in the N-terminal domain of the 51-kDa FK506-binding protein (FKBP51) near its site of interaction with the steroid receptor proteins
by LeMaster, David M and Mustafi, Sourajit M and Brecher, Matthew and Zhang, Jing and Héroux, Annie and Li, Hongmin and Hernández, Griselda and Brookhaven National Laboratory (BNL), Upton, NY (United States)
Journal of Biological Chemistry, ISSN 0021-9258, 06/2015, Volume 290, Issue 25, pp. 15746 - 15757
Background: FK506-binding protein 51 (FKBP51) inhibits and FKBP52 stimulates transcription by various steroid receptors. Exchange of a single residue largely... 
HSP90 | ACTIVE-SITE | BIOCHEMISTRY & MOLECULAR BIOLOGY | GR-ALPHA | RELAXATION | allosteric regulation | CHEMICAL-EXCHANGE | conformational change | x-ray crystallography | GLUCOCORTICOID-RECEPTOR | nuclear magnetic resonance (NMR) | DYNAMICS | prolyl isomerase | PROGESTERONE-RECEPTOR | BINDING | ASSOCIATION | Protein Structure, Tertiary | Protein Structure, Secondary | Tacrolimus Binding Proteins - chemistry | Humans | Receptors, Androgen - metabolism | Models, Molecular | Receptors, Glucocorticoid - metabolism | Tacrolimus Binding Proteins - metabolism | Mutation, Missense | Tacrolimus Binding Proteins - genetics | Receptors, Androgen - genetics | Protein Structure, Quaternary | Receptors, Glucocorticoid - genetics | Nuclear Magnetic Resonance, Biomolecular | Receptors, Androgen - chemistry | Receptors, Glucocorticoid - chemistry | Amino Acid Substitution | MATERIALS SCIENCE | Protein Structure and Folding
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7. Full Text The receptor proteins： pivotal roles in selective autophagy
by Zhijie Xu Lifang Yang San Xu Zhibao Zhang Ya Cao
生物化学与生物物理学报：英文版, ISSN 1672-9145, 2015, Volume 47, Issue 8, pp. 571 - 580
Autophagy is a highly regulated and multistep biological process whereby cells under metabolic, proteotoxic, or other stresses remove dysfunctional organelles... 
降解蛋白 | 应力消除 | 自噬作用 | 生物过程 | 受体蛋白 | 细胞代谢 | BRCA1 | 错误折叠 | Autophagy | Selective | Receptor proteins | REGULATE AUTOPHAGY | ANDROGEN RECEPTOR | autophagy | selective | PARKIN-MEDIATED MITOPHAGY | UBIQUITIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | LIR MOTIF | P62 | CARGO RECEPTOR | PINK1/PARKIN-MEDIATED MITOPHAGY | BIOPHYSICS | STRUCTURAL BASIS | receptor proteins | CBL FAMILY | Organelle Biogenesis | Proteins - physiology | Adaptor Proteins, Signal Transducing - physiology | Animals | Proteolysis | Sequestosome-1 Protein | Humans | Receptors, Cytoplasmic and Nuclear - physiology | Autophagy - physiology | Index Medicus
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8. Full Text Heat Shock Protein 70 Chaperone Overexpression Ameliorates Phenotypes of the Spinal and Bulbar Muscular Atrophy Transgenic Mouse Model by Reducing Nuclear-Localized Mutant Androgen Receptor Protein
by Adachi, Hiroaki and Katsuno, Masahisa and Minamiyama, Makoto and Sang, Chen and Pagoulatos, Gerassimos and Angelidis, Charalampos and Kusakabe, Moriaki and Yoshiki, Atsushi and Kobayashi, Yasushi and Doyu, Manabu and Sobue, Gen
Journal of Neuroscience, ISSN 0270-6474, 03/2003, Volume 23, Issue 6, pp. 2203 - 2211
Spinal and bulbar muscular atrophy (SBMA) is an inherited motor neuron disease caused by the expansion of the polyglutamine ( polyQ) tract within the androgen... 
Protein degradation | HSP70 | Polyglutamine | SBMA | Chaperone | Transgenic mice | EXPANDED POLYGLUTAMINE | INHIBITS HUNTINGTIN AGGREGATION | MOLECULAR CHAPERONES | polyglutamine | BINDING PROTEIN | SUPPRESSION | NEUROSCIENCES | CELLULAR TOXICITY | chaperone | transgenic mice | DISEASE | N-TERMINAL HUNTINGTIN | CYTOCHROME-C RELEASE | protein degradation | Immunohistochemistry | Humans | Receptors, Androgen - metabolism | Male | Muscular Atrophy, Spinal - genetics | Cell Nucleus - metabolism | Cell Nucleus - pathology | Muscular Atrophy, Spinal - physiopathology | Disease Models, Animal | HSP70 Heat-Shock Proteins - biosynthesis | Molecular Chaperones - biosynthesis | Gene Expression | Molecular Chaperones - genetics | HSP70 Heat-Shock Proteins - genetics | Mice, Transgenic | Muscular Atrophy, Spinal - pathology | Blotting, Western | Disease Progression | Macromolecular Substances | Motor Activity - genetics | Phenotype | Animals | Receptors, Androgen - genetics | Trinucleotide Repeat Expansion - genetics | Mice | Mutation | Crosses, Genetic | ARTICLE
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9. Full Text NRIP/DCAF6 stabilizes the androgen receptor protein by displacing DDB2 from the CUL4A-DDB1 E3 ligase complex in prostate cancer
by Chen, Hsin-Hsiung and Fan, Ping and Chang, Szu-Wei and Tsao, Yeou-Ping and Huang, Hsiang-Po and Chen, Show-Li
Oncotarget, ISSN 1949-2553, 2017, Volume 8, Issue 13, pp. 21501 - 21515
Both nuclear receptor interaction protein (NRIP) and DNA damage binding protein 2 (DDB2) belong to the Cullin 4 (CUL4)-DDB1 binding protein family and are... 
Cribriform prostate cancer | Cul4-DDB1 | NRIP/DCAF6 | DDB2 | CELLS | DUCTAL ADENOCARCINOMA | DNA-DAMAGE | CRIBRIFORM PATTERN | BINDING-PROTEIN | OVARIAN-CANCER | CELL BIOLOGY | BREAST-CANCER | LUNG-CANCER | CUL4-DDB1 UBIQUITIN LIGASE | cribriform prostate cancer | TUMOR-SUPPRESSOR | Immunohistochemistry | Prostatic Neoplasms - metabolism | Prostatic Neoplasms - pathology | Immunoprecipitation | Humans | Receptors, Androgen - metabolism | Male | Nuclear Proteins - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | DNA-Binding Proteins - metabolism | Cullin Proteins - metabolism | Protein Stability | Adaptor Proteins, Signal Transducing - metabolism
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10. Full Text Artemisinin disrupts androgen responsiveness of human prostate cancer cells by stimulating the 26S proteasome-mediated degradation of the androgen receptor protein
by Steely, Andrea M and Willoughby, Jamin A and Sundar, Shyam N and Aivaliotis, Vasiliki I and Firestone, Gary L
Anti-Cancer Drugs, ISSN 0959-4973, 10/2017, Volume 28, Issue 9, pp. 1018 - 1031
Androgen receptor (AR) expression and activity is highly linked to the development and progression of prostate cancer and is a target of therapeutic strategies... 
prostate cancer cells | APOPTOSIS | DIHYDROARTEMISININ | PHOSPHORYLATION | antiproliferative signaling | ANTIMALARIAL | artemisinin | ONCOLOGY | PATHWAY | GROWTH | LNCAP CELLS | AKT-1 | PHARMACOLOGY & PHARMACY | androgen receptor degradation | CYTOTOXICITY | EXPRESSION | CYCLE | Prostatic Neoplasms - metabolism | Humans | Receptors, Androgen - metabolism | Male | Phosphatidylinositol 3-Kinases - metabolism | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Proto-Oncogene Proteins c-akt - genetics | Artemisinins - pharmacology | Prostatic Neoplasms - genetics | Ubiquitination - drug effects | Transcription, Genetic | Prostate-Specific Antigen - metabolism | Phosphorylation - drug effects | Chromones - pharmacology | Proto-Oncogene Proteins c-akt - metabolism | Proto-Oncogene Proteins c-mdm2 - metabolism | Prostatic Neoplasms - drug therapy | Prostate-Specific Antigen - genetics | Enzyme Inhibitors - pharmacology | Kallikreins - genetics | Morpholines - pharmacology | Down-Regulation - drug effects | Phosphatidylinositol 3-Kinases - genetics | Receptors, Androgen - genetics | Cell Line, Tumor | Mutation | Proteasome Endopeptidase Complex - metabolism | Kallikreins - metabolism
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11. Full Text Estrogen receptor protein content is different in abdominal than gluteal subcutaneous adipose tissue of overweight-to-obese premenopausal women
by Gavin, Kathleen M and Cooper, Elizabeth E and Hickner, Robert C
Metabolism, ISSN 0026-0495, 2013, Volume 62, Issue 8, pp. 1180 - 1188
Abstract Objective Premenopausal women demonstrate a distinctive gynoid body fat distribution and circulating estrogen status is associated with the... 
Endocrinology & Metabolism | Caucasian | Sex steroid receptors | Body fat distribution | Estradiol | African American | VISCERAL FAT | DISEASE RISK-FACTORS | POSTMENOPAUSAL HORMONE-THERAPY | AFRICAN-AMERICAN | ER-ALPHA | BETA | BODY-FAT | REGIONAL FAT DISTRIBUTION | INSULIN-RESISTANCE | ENDOCRINOLOGY & METABOLISM | CARDIOVASCULAR-DISEASE | Buttocks | United States | Humans | European Continental Ancestry Group | Receptors, G-Protein-Coupled - biosynthesis | Gonadal Steroid Hormones - blood | Blotting, Western | Obesity - metabolism | Young Adult | Overweight - metabolism | Abdominal Fat - metabolism | Subcutaneous Fat - metabolism | Biopsy | Estrogen Receptor beta - biosynthesis | Lipids - blood | Adolescent | Receptors, Estrogen - biosynthesis | Adult | Female | Estrogen Receptor alpha - biosynthesis | African Continental Ancestry Group | Premenopause - metabolism | Body Composition - physiology | Women | Adipose tissues | Obesity | Menopause | Low density lipoproteins | Estrogen | Hormones | Sulfates | Cholesterol | Dehydroepiandrosterone | Androgens | Analysis | Phenols | Insulin resistance | G proteins
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12. Full Text Effect of resistance exercise on muscle steroid receptor protein content in strength-trained men and women
by Vingren, Jakob L and Kraemer, William J and Hatfield, Disa L and Volek, Jeff S and Ratamess, Nicholas A and Anderson, Jeffrey M and Häkkinen, Keijo and Ahtiainen, Juha and Fragala, Maren S and Thomas, Gwendolyn A and Ho, Jen-Yu and Maresh, Carl M
Steroids, ISSN 0039-128X, 2009, Volume 74, Issue 13, pp. 1033 - 1039
The purpose of this study was to examine the acute effect of resistance exercise (RE) on muscle androgen receptor (AR) and glucocorticoid receptor (GR) protein... 
Testosterone | Endocrine | Exercise training | Androgen receptor | Glucocorticoid receptor | ACUTE HORMONAL RESPONSES | BIOCHEMISTRY & MOLECULAR BIOLOGY | HEAVY-RESISTANCE | BODY-COMPOSITION | SKELETAL-MUSCLE | GLUCOCORTICOID-RECEPTOR | MESSENGER-RNA | NANDROLONE DECANOATE | ENDOCRINOLOGY & METABOLISM | OLDER MEN | Humans | Receptors, Androgen - metabolism | Male | Muscle, Skeletal - metabolism | Receptors, Glucocorticoid - metabolism | Muscle, Skeletal - cytology | Resistance Training | Young Adult | Exercise | Sex Factors | Adult | Female | Testosterone - blood | Physiological aspects | Corticosteroids | Universities and colleges | Analysis
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13. Full Text Alteration of androgen receptor protein stability by triptolide in LNCaP cells
by Li, Wei and Liu, Bi-De and Liao, Kai and Liu, Yong and Wan, Zi-Jin and Dong, Yu-Fen and Cao, Qian-Qian and Zhu, Qian and Xiao, Gu
Medicina (Lithuania), ISSN 1010-660X, 07/2018, Volume 54, Issue 3, p. 39
Background and Objective: Although triptolide was effective for prostate cancer (PCa), the mechanism is still unclear. Androgen receptor (AR) plays a large... 
Calpain | Protein stability | Triptolide | Androgen receptor | PROSTATE | ACTIVATION | PHOSPHORYLATION | triptolide | protein stability | calpain | MEDICINE, GENERAL & INTERNAL | androgen receptor | AMPLIFICATION | INHIBITION | GENE | DEGRADATION | CANCER STATISTICS | EXPRESSION
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14. Full Text Association between cadmium and androgen receptor protein expression differs in prostate tumors of African American and European American men
by Neslund-Dudas, Christine M and McBride, Russell B and Kandegedara, Ashoka and Rybicki, Benjamin A and Kryvenko, Oleksandr N and Chitale, Dhananjay and Gupta, Nilesh and Williamson, Sean R and Rogers, Craig G and Cordon-Cardo, Carlos and Rundle, Andrew G and Levin, Albert M and Dou, Q. Ping and Mitra, Bharati
Journal of Trace Elements in Medicine and Biology, ISSN 0946-672X, 07/2018, Volume 48, pp. 233 - 238
Cadmium is a known carcinogen that has been implicated in prostate cancer, but how it affects prostate carcinogenesis in humans remains unclear. Evidence from... 
Cadmium | Prostate cancer | Androgen receptor | Heavy metal | African American | RACE/ETHNICITY | DNA-ADDUCTS | POLYCYCLIC AROMATIC-HYDROCARBON | BIOCHEMISTRY & MOLECULAR BIOLOGY | NATIONAL-HEALTH | SMOKING | CANCER | GENE | ENDOCRINOLOGY & METABOLISM | MENTHOL CIGARETTES | EXPOSURE | Prostatic Neoplasms - metabolism | Receptors, Androgen - biosynthesis | United States | Humans | Middle Aged | African Americans | Cadmium - analysis | European Continental Ancestry Group | Male | Prostate-specific antigen | Zinc in the body | Development and progression | Mass spectrometry | Tumors | Index Medicus | heavy metal | cadmium | prostate cancer | androgen receptor
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15. Full Text Quantitative characterization of androgen receptor protein expression and cellular localization in circulating tumor cells from patients with metastatic castration-resistant prostate cancer
by Reyes, Edwin E and Vander Weele, David J and Isikbay, Masis and Duggan, Ryan and Campanile, Alexa and Stadler, Walter M and Vander Griend, Donald J and Szmulewitz, Russell Z
Journal of Translational Medicine, ISSN 1479-5876, 2014, Volume 12, Issue 1, p. 313
Background: Many current therapies for metastatic castration-resistant prostate cancer (mCRPC) are aimed at AR signaling; however, resistance to these... 
Castration-resistant prostate cancer | Prostate neoplasms | Circulating tumor cells | Androgen receptor | LEUKEMIA GROUP-B | SURVIVAL | MEDICINE, RESEARCH & EXPERIMENTAL | BIOMARKER | VARIANTS | PERIPHERAL-BLOOD | THERAPY | AMPLIFICATION | GENE | CARCINOMA | PROGRESSION | Prostatic Neoplasms - metabolism | Prostatic Neoplasms - pathology | Humans | Middle Aged | Receptors, Androgen - metabolism | Male | Feasibility Studies | Orchiectomy | Neoplasm Metastasis | Flow Cytometry | Neoplastic Cells, Circulating | Aged, 80 and over | Prostatic Neoplasms - blood | Aged | Medicine, Experimental | Medical research | Care and treatment | Prostate cancer | Flow cytometry | Laboratories | Mortality | Colleges & universities | Metastasis | Cancer therapies | Patients | Blood | Proteins | Androgens | Microscopy | Biopsy | Medical prognosis | Protein expression | Deoxyribonucleic acid--DNA | Questioning
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