The DOI matches its Crossref record; 363 of the 375 references it cites were found in a registry or an index.
Androgen Receptor (AR) Coregulators: A Diversity of Functions Converging on and Regulating the AR Transcriptional Complex
Abstract
Androgens, acting through the androgen receptor (AR), are responsible for the development of the male phenotype during embryogenesis, the achievement of sexual maturation at puberty, and the maintenance of male reproductive function and behavior in adulthood. In addition, androgens affect a wide variety of nonreproductive tissues. Moreover, aberrant androgen action plays a critical role in multiple pathologies, including prostate cancer and androgen insensitivity syndromes. The formation of a productive AR transcriptional complex requires the functional and structural interaction of the AR with its coregulators. In the last decade, an overwhelming and ever increasing number of proteins have been proposed to possess AR coactivating or corepressing characteristics. Intriguingly, a vast diversity of functions has been ascribed to these proteins, indicating that a multitude of cellular functions and signals converge on the AR to regulate its function. The current review aims to provide an overview of the AR coregulator proteins identified to date and to propose a classification of these AR coregulator proteins according to the function(s) ascribed to them. Taken together, this approach will increase our understanding of the cellular pathways that converge on the AR to ensure an appropriate transcriptional response to androgens.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Androgen receptors can be modulated by specific proteins called coregulators [70–72] or mediated via the activation of membrane-bound protein receptors to initiate intracellular signalling pathways [73], which can occur even in the presence of low levels of androgens [74].”
From Integrating Transwomen and Female Athletes with Differences of Sex Development (DSD) into Elite Competition: The FIMS 2021 Consensus Statement (2021) · cites this paper as [71]
Citations
Cites
The Role of Chromatin during Transcription
Li, B., Carey, M., & Workman, J. L. (2007) · Cell · doi:10.1016/j.cell.2007.01.015 · Cited by 3,503
MOLECULAR MECHANISMS OF ACTION OF STEROID/THYROID RECEPTOR SUPERFAMILY MEMBERS
Tsai, M., & O’Malley, B. W. (1994) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.63.070194.002315 · Cited by 2,887
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
Spada, A. L., Wilson, E. M., Lubahn, D. B., Harding, A., & Fischbeck, K. (1991) · Nature · doi:10.1038/352077a0 · Cited by 2,801
Sequence and Characterization of a Coactivator for the Steroid Hormone Receptor Superfamily
Oñate, S. A., Tsai, S. Y., Tsai, M., & O’Malley, B. W. (1995) · Science · doi:10.1126/science.270.5240.1354 · Cited by 2,398
A signature motif in transcriptional co-activators mediates binding to nuclear receptors
Heery, D. M., Kalkhoven, E., Hoare, S., & Parker, M. G. (1997) · Nature · doi:10.1038/42750 · Cited by 2,128
LSD1 demethylates repressive histone marks to promote androgen-receptor-dependent transcription
Metzger, E., Wissmann, M., Yin, N., Müller, J. M., Schneider, R., Peters, A. H. F. M., Günther, T., Buettner, R., & Schüle, R. (2005) · Nature · doi:10.1038/nature04020 · Cited by 1,780
Androgen Receptor Defects: Historical, Clinical, and Molecular Perspectives*
Quigley, C. A., Bellis, A. D., Marschke, K. B., Awady, M. K. E., Wilson, E. M., & French, F. S. (1995) · Endocrine Reviews · doi:10.1210/edrv-16-3-271 · Cited by 1,459
Proteasome-Independent Functions of Ubiquitin in Endocytosis and Signaling
Mukhopadhyay, D., & Riezman, H. (2007) · Science · doi:10.1126/science.1127085 · Cited by 1,221
Regulation of Transcription by a Protein Methyltransferase
Chen, D., Ma, H., Hong, H., Koh, S. S., Huang, S., Schurter, B. T., Aswad, D. W., & Stallcup, M. R. (1999) · Science · doi:10.1126/science.284.5423.2174 · Cited by 1,214
Steroid 5α-reductase: two genes/two enzymes
Russell, D. W., & Wilson, J. D. (1994) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.63.070194.000325 · Cited by 1,105
Research works printed but not linked: 1
- Litvinov, 2003, Is the Achilles’ heel for prostate cancer therapy a gain of function in androgen receptor signaling?, J Clin Endocrinol Metab, 88, 2972, 10.1210/jc.2002-022038 · DOI
Cited by
Sorted by citations
Items 701–753 of 753
Developing Isoxazole as a Native Photo‐Cross‐Linker for Photoaffinity Labeling and Chemoproteomics
Cheng, K., Qi, J., Ren, X., Zhang, J., Li, H., Xiao, H., Wang, R. Y., Liu, Z., Meng, L., Ma, N., et al. (2022) · Angewandte Chemie · doi:10.1002/ange.202209947
El-Azeem, M. A. A., & Radi, D. A. (2023) · Journal of Microscopy and Ultrastructure · doi:10.4103/jmau.jmau_119_22
Howe, C. G., Liu, X., Hall, M. N., Ilievski, V., Caudill, M. A., Malysheva, O., Lomax-Luu, A. M., Parvez, F., Siddique, A. B., Shahriar, H., et al. (2023) · doi:10.1158/1055-9965.c.6515538
Wei, J., Yin, L., Li, J., Wang, J., Pu, T., Duan, P., Lin, T., Gao, A. C., & Wu, B. J. (2023) · doi:10.1158/0008-5472.c.6513082.v1
Heemers, H. V., Schmidt, L. J., Sun, Z., Regan, K. M., Anderson, S. K., Duncan, K., Wang, D., Liu, S., Ballman, K. V., & Tindall, D. J. (2023) · doi:10.1158/0008-5472.c.6503106.v1
Self-citationJiménez‐Vacas, J. M., Montero‐Hidalgo, A. J., Gómez‐Gómez, E., Sáez-Martínez, P., Pérez‐Gómez, J. M., Fuentes-Fayos, A. C., Blázquez‐Encinas, R., Sánchez‐Sánchez, R., Gonzalez-Serrano, T., Castro, E., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2885147/v1
Androgen Receptor Signaling: A Central and Evolving Theme in Prostate Cancer Treatment
Banerjee, P. P., & Srivastava, S. K. (2023) · Springer eBooks · doi:10.1007/978-981-99-2196-6_24-1
Investigating the role of mitochondrial energy rewiring throughout prostate cancer progression
Bidgood, C. L. (2023) · Queensland University of Technology · doi:10.5204/thesis.eprints.248849
Androgen Receptor Signaling: A Central and Evolving Theme in Prostate Cancer Treatment
Banerjee, P. P., & Srivastava, S. K. (2024) · Springer eBooks · doi:10.1007/978-981-99-6263-1_24 · Cited by 1
Androgenrezeptor in Gesundheit und Krankheit
Hohl, A., & Marcelli, M. (2024) · Springer eBooks · doi:10.1007/978-3-031-65245-5_2
Reproductive and nonreproductive actions of testosterone
Gagliano‐Jucá, T., Jain, A., Jasuja, R., & Bhasin, S. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-13825-6.00198-9
Boldrini, L., Watts, S., Schneider, N., Saravanan, R., & Bardi, M. (2025) · Sci · doi:10.3390/sci7030111
Zhang, Y., Jin, Z., Wu, Y. M., Tang, X., Wang, C., Wang, S., Li, Y., Zhang, T., Jin, F., Lu, H., et al. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01489-5
Rho Small GTPase Family in Androgen-Regulated Prostate Cancer Progression and Metastasis
Hairston, D. W. S., Mudryj, M. M., & Ghosh, P. (2025) · Cancers · doi:10.3390/cancers17223680
Precision Medicine in Prostate Cancer: The Role of Molecular Diagnostics and Targeted Therapies
Guedouar, A., & Roumieh, E. (2025) · annals of urologic oncology · doi:10.32948/auo.2025.10.15
Maluf, F. C., da Silva, K. S., Caetano, G. V. B., Brito, P. H. S., Candido, P., dos Santos, G. A., Guimarães, V. R., Silva, I. A., Antunes, A. A., Leite, K. R. M., et al. (2025) · Biomedicines · doi:10.3390/biomedicines13122896
Agarwal, A., Patnaik, A., Gupta, E., Jaiswal, B., & Gupta, A. K. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.117616
Zhu, H., Yao, H., Xu, Y., Chen, Y., Han, B., Wang, N., Wang, H., Zhang, Q., Zhu, W., Shi, Y., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14431988
Zhu, H., Yao, H., Xu, Y., Chen, Y., Han, B., Wang, N., Wang, H., Zhang, Q., Zhu, W., Shi, Y., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14431994
Zhu, H., Yao, H., Xu, Y., Chen, Y., Han, B., Wang, N., Wang, H., Zhang, Q., Zhu, W., Shi, Y., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14431991
Videira, A., Beckedorff, F., daSilva, L. F., & Verjovski‐Almeida, S. (2021) · Figshare · doi:10.6084/m9.figshare.13558765
Videira, A., Beckedorff, F., daSilva, L. F., & Verjovski‐Almeida, S. (2021) · Figshare · doi:10.6084/m9.figshare.13558762
Chellini, L., Pieraccioli, M., Sette, C., & Paronetto, M. P. (2022) · Figshare · doi:10.6084/m9.figshare.19799911
Liu, Y., Qian, D., Ding, Y., Wu, D., Tang, C., Xu, C., & Chen, X. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.149810
Paakinaho, V., Sutinen, P., Malinen, M., & Palvimo, J. J. (2026) · Endocrinology · doi:10.1007/978-3-319-29456-8_12-2
Métabolisme oxydatif et mitochondrial des cellules cancéreuses de prostate
Matar, C. (2011) · theses.fr (ABES) · doi:10.70675/6abb943ez119bz424fzbe51z3467241fc235
La Neuropiline-1, un nouveau biomarqueur de résistance thérapeutique du cancer de la prostate
Blanc, C. (2016) · theses.fr (ABES) · doi:10.70675/b45322c5z1cbdz42c4zba0azdb401927d53c
Genome-wide analyses of signaling pathways controlled by steroid receptors
Rerra, A. (2019) · theses.fr (ABES) · doi:10.70675/d10332bfzd22cz480cz8f5czc0114d6c93c5
Characterization of Pten and Trp53 deficient prostatic tumors in mice
Bizri, R. E. (2018) · theses.fr (ABES) · doi:10.70675/887a45dbz93f0z4790z9840z71a317de4d2f
Grolez, G. P. (2018) · theses.fr (ABES) · doi:10.70675/dc6166d1z44efz4faezaf84zdeca8a743229
Madi-Berthélémy, P. O. (2018) · theses.fr (ABES) · doi:10.70675/451e797fz4661z4896z886bz419b6d675751
Biomarqueurs circulants dans le cancer de la prostate métastatique résistant à la castration
Maillet, D. (2022) · theses.fr (ABES) · doi:10.70675/c764fae7z7ddcz4e95z96bez5039c3575f58
Role of long non-coding RNAs in prostate cancer progression
Cipolla, R. (2023) · theses.fr (ABES) · doi:10.70675/629b8b5dz2fe3z478dz87c4z97664da47d1e
Hamilton, R. A., Paul, B., Yi, P., Rajapakshe, K., Panigrahi, A. K., Grimm, S. L., Coarfa, C., Malovannaya, A., Weigel, N. L., Lonard, D. M., et al. (2026) · PLoS ONE · doi:10.1371/journal.pone.0349130
Veluthakunju, A. E., Puvvada, S., Kumar, S. S., Eralil, G. J., Chettiyar, A. D., Edatholath, J., Chalil, J. V., William, A., Sundaresh, A., & Divakaran, D. R. (2026) · Fertility & Reproduction · doi:10.1142/s2661318226300047
Liu, X., Koga, K., Noguchi, M., Hirata, M., Yasukochi, Y., & Nagahama, K. (2026) · The Journal of Biochemistry · doi:10.1093/jb/mvag049
Short Linear Motifs as a General Organizing Principle of the Nuclear-Receptor Proximal InteractomePreprint
Eng, J. K., Radoshevich, L., & Wright, M. E. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.06.743235
Effects of fenpropathrin on adult zebrafish reproduction and offspring development
Li, J., Song, H., Jiang, Z., Zhu, Y., Sultan, Y., Li, Y., & Ding, W. (2026) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2026.107353
BindingDB (2026) · UC San Diego · doi:10.7270/q2g44w4d
Elguero, M. B. (2013) · Repositorio Digital Institucional de la Universidad de Buenos Aires (Universidad de Buenos Aires)
Ridden, A. D. (2013) · UC Research Repository (University of Canterbury) · doi:10.26021/6519
Targeting the genes of 9p13.3 amplicon in prostate cancer
Grönlund, T. (2015) · Tampere University Institutional Repository (Tampere University)
Genetics and Genito-Urinary Cancer
Morris, M. R., & Maher, E. R. (2014) · Springer eBooks · doi:10.1007/978-0-85729-482-1_3
Metadata
- Authors
- Heemers, H. V., & Tindall, D. J.
- Affiliations
- Mayo Clinic (US)
- Corresponding author
- Tindall, Donald J.
- Venue
- Endocrine Reviews
- Publisher
- The Endocrine Society
- Published
- 2007-10-16
- Volume
- 28
- Issue
- 7
- Pages
- 778-808
- ISSN
- 0163-769X (ISSN-L)
- 1945-7189
- OpenAlex
- W2164092182
- Cited by
- 753
- References
- 375
- Citations by year
- 2026: 12 · 2025: 26 · 2024: 30 · 2023: 29 · 2022: 40 · 2021: 48 · 2020: 26 · 2019: 37 · 2018: 37 · 2017: 38 · 2016: 54 · 2015: 49 · 2014: 42 · 2013: 70 · 2012: 52
- FWCI
- 5.79
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Endocrine Reviews (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (R01CA121277, CA125747, R01CA125747, CA 91956, CA121277, P50CA091956, CA 15083, P30CA015083)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK065236, DK65236)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Prostate Cancer Treatment and Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Estrogen and related hormone effects
- Health Sciences › Medicine › Reproductive Medicine › Sperm and Testicular Function
- Keywords
- androgen receptor, coregulators, transcriptional coactivator, corepressors, transcriptional complex, androgen signaling, male reproductive development, prostate cancer, androgen insensitivity syndrome
- MeSH terms
- Androgens, Gene Expression Regulation, Humans, Male, Receptors, Androgen, Transcription Factors
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review