The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Constitutively active androgen receptor splice variants expressed in castration-resistant prostate cancer require full-length androgen receptor.
Open accessAbstract
Androgen receptor (AR) splice variants lacking the ligand binding domain (ARVs), originally isolated from prostate cancer cell lines derived from a single patient, are detected in normal and malignant human prostate tissue, with the highest levels observed in late stage, castration-resistant prostate cancer. The most studied variant (called AR-V7 or AR3) activates AR reporter genes in the absence of ligand and therefore, could play a role in castration resistance. To explore the range of potential ARVs, we screened additional human and murine prostate cancer models using conventional and next generation sequencing technologies and detected several structurally diverse AR isoforms. Some, like AR-V7/AR3, display gain of function, whereas others have dominant interfering activity. We also find that ARV expression increases acutely in response to androgen withdrawal, is suppressed by testosterone, and in some models, is coupled to full-length AR (AR-FL) mRNA production. As expected, constitutively active, ligand-independent ARVs such as AR-V7/AR3 are sufficient to confer anchorage-independent (in vitro) and castration-resistant (in vivo) growth. Surprisingly, this growth is blocked by ligand binding domain-targeted antiandrogens, such as MDV3100, or by selective siRNA silencing of AR-FL, indicating that the growth-promoting effects of ARVs are mediated through AR-FL. These data indicate that the increase in ARV expression in castrate-resistant prostate cancer is an acute response to castration rather than clonal expansion of castration or antiandrogen-resistant cells expressing gain of function ARVs, and furthermore, they provide a strategy to overcome ARV function in the clinic.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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
“The activity of these variants still depends on the presence of a full-length AR, although treatment with the AR antagonist MDV3100 or siRNA knockdown of full-length AR inhibited transcription and androgen-free growth (77).”
From Minireview: Alternative Activation Pathways for the Androgen Receptor in Prostate Cancer (2011) · cites this paper as [77]
In the citing paper
“Moreover, the constitutive activity attributed to some variants may still rely on the presence of the full-length AR to mediate binding of AR to DNA and stimulate transcription (77).”
From Minireview: Alternative Activation Pathways for the Androgen Receptor in Prostate Cancer (2011) · cites this paper as [77]
In the citing paper
“In one study, endogenous expression of variant mRNA in patient samples and xenografts is much lower (ϳ0.1-2.5%)relative to full-length AR mRNA (77).”
From Minireview: Alternative Activation Pathways for the Androgen Receptor in Prostate Cancer (2011) · cites this paper as [77]
In the citing paper
“Interestingly, comparison of the transcriptome of variants with that of full-length AR suggests a significant amount of target specificity for each variant (76 -78).”
From Minireview: Alternative Activation Pathways for the Androgen Receptor in Prostate Cancer (2011) · cites this paper as [77]
In the citing paper
“Two such variants, human AR-V7, identified in CR prostate cancer specimens, and mouse AR-V4, from the murine Myc-CaP cell line, demonstrate ligand-free activation of a 4xARE-Luc promoter as well as promoting CR LNCaP tumor growth.”
From Minireview: Alternative Activation Pathways for the Androgen Receptor in Prostate Cancer (2011) · cites this paper as [77]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
TopHat: discovering splice junctions with RNA-Seq
Trapnell, C., Pachter, L. S., & Salzberg, S. L. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp120 · Cited by 11,682
Development of a second-generation antiandrogen for treatment of advanced prostate cancer.
Tran, C., Ouk, S., Clegg, N. J., Chen, Y., Watson, P. A., Arora, V., Wongvipat, J., Smith-Jones, P. M., Yoo, D., Kwon, A., et al. (2009) · Science · doi:10.1126/science.1168175 · Cited by 2,292
Self-citationHu, R., Dunn, T. A., Wei, S., Isharwal, S., Veltri, R. W., Humphreys, E., Han, M., Partin, A. W., Vessella, R. L., Isaacs, W. B., et al. (2009) · Cancer Research · doi:10.1158/0008-5472.can-08-2764 · Cited by 1,077
Antitumour activity of MDV3100 in castration-resistant prostate cancer: a phase 1–2 study
Scher, H. I., Beer, T. M., Higano, C. S., Anand, A., Taplin, M., Efstathiou, E., Rathkopf, D. E., Shelkey, J., Yu, E. Y., Alumkal, J. J., et al. (2010) · The Lancet · doi:10.1016/s0140-6736(10)60172-9 · Cited by 1,063
Scher, H. I., & Sawyers, C. L. (2005) · Journal of Clinical Oncology · doi:10.1200/jco.2005.03.4777 · Cited by 1,025
Self-citationGuo, Z., Yang, X., Sun, F., Jiang, R., Linn, D. E., Chen, H., Chen, H., Kong, X., Melamed, J., Tepper, C. G., et al. (2009) · Cancer Research · doi:10.1158/0008-5472.can-08-3795 · Cited by 880
Dehm, S. M., Schmidt, L. J., Heemers, H. V., Vessella, R. L., & Tindall, D. J. (2008) · Cancer Research · doi:10.1158/0008-5472.can-08-0594 · Cited by 834
Sun, S., Sprenger, C. C. T., Vessella, R. L., Haugk, K., Soriano, K., Mostaghel, E. A., Page, S. T., Coleman, I. M., Nguyen, H. M., Sun, H., et al. (2010) · Journal of Clinical Investigation · doi:10.1172/jci41824 · Cited by 748
He, B., Kemppainen, J., & Wilson, E. M. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m002807200 · Cited by 441
Molecular basis of androgen insensitivity
Brinkmann, A. O. (2001) · Molecular and Cellular Endocrinology · doi:10.1016/s0303-7207(01)00466-x · Cited by 345
Cited by
Sorted by citations
Items 301–400 of 643
ARVib suppresses growth of advanced prostate cancer via inhibition of androgen receptor signaling
Liu, C., Armstrong, C. M., Ning, S., Yang, J. C., Lou, W., Lombard, A. P., Zhao, J., Wu, C., Yu, A., Evans, C. P., et al. (2021) · Oncogene · doi:10.1038/s41388-021-01914-2 · Cited by 30
Streicher, W., Luedeke, M., Azoitei, A., Zengerling, F., Herweg, A., Genze, F., Schrader, M. G., Schrader, A. J., & Cronauer, M. V. (2014) · PLoS ONE · doi:10.1371/journal.pone.0098566 · Cited by 28
Li, J., Zhang, B., Liu, M., Fu, X., Ci, X., Jun, A., Fu, C., Dong, G., Wu, R., Zhang, Z., et al. (2020) · Cancers · doi:10.3390/cancers12030748 · Cited by 25
Prognostic role of TSPAN1, KIAA1324 and ESRP1 in prostate cancer
Stinnesbeck, M., Kristiansen, A., Ellinger, J., Hauser, S., Egevad, L., Tolkach, Y., & Kristiansen, G. (2021) · Apmis · doi:10.1111/apm.13117 · Cited by 26
Biron, É., & Bédard, F. (2015) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2015.07.006 · Cited by 27
Activation of GRP/GRP-R signaling contributes to castration-resistant prostate cancer progression
Qiao, J., Grabowska, M. M., Forestier-Román, I., Mirosevich, J., Case, T. C., Chung, D. H., Cates, J., Matusik, R. J., Manning, H. C., & Jin, R. (2016) · Oncotarget · doi:10.18632/oncotarget.11326 · Cited by 26
Thyroid and androgen receptor signaling are antagonized by μ‐Crystallin in prostate cancer
Aksoy, O., Pěnčík, J., Hartenbach, M., Moazzami, A. A., Schlederer, M., Balber, T., Varady, A., Philippe, C., Baltzer, P., Mazumder, B., et al. (2020) · International Journal of Cancer · doi:10.1002/ijc.33332 · Cited by 26
Dellis, A., & Papatsoris, A. (2018) · Expert Opinion on Pharmacotherapy · doi:10.1080/14656566.2018.1548611 · Cited by 24
Kim, S., Au, C. C., Jamalruddin, M. A. B., Abou-Ghali, N. E., Mukhtar, E., Portella, L., Berger, A., Worroll, D., Vatsa, P., Rickman, D. S., et al. (2022) · eLife · doi:10.7554/elife.73396 · Cited by 25
Sun, R., Wei, T., Ding, D., Zhang, J., Chen, S., He, H. H., Wang, L., & Huang, H. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2205509119 · Cited by 26
Androgen receptor aberrations in the era of abiraterone and enzalutamide
Jentzmik, F., Azoitei, A., Zengerling, F., Damjanoski, I., & Cronauer, M. V. (2015) · World Journal of Urology · doi:10.1007/s00345-015-1624-2 · Cited by 26
Ramamurthy, V. P., Ramalingam, S., Gediya, L. K., Kwegyir‐Afful, A. K., & Njar, V. C. O. (2014) · Oncotarget · doi:10.18632/oncotarget.3084 · Cited by 25
WOMEN IN CANCER THEMATIC REVIEW: New roles for nuclear receptors in prostate cancer
Leach, D. A., Powell, S. M., & Bevan, C. L. (2016) · Endocrine Related Cancer · doi:10.1530/erc-16-0319 · Cited by 25
Cancer and the metastatic substrate
Arvelo, F. A., Sojo, F. J., & Cotte, C. (2016) · ecancermedicalscience · doi:10.3332/ecancer.2016.701 · Cited by 25
Xu, D., Chen, Q., Liu, Y., & Wen, X. (2017) · Oncotarget · doi:10.18632/oncotarget.22319 · Cited by 25
A unifying biology of sex steroid-induced apoptosis in prostate and breast cancers
Maximov, P. Y., Abderrahman, B., Curpan, R. F., Hawsawi, Y. M., Fan, P., & Jordan, V. C. (2017) · Endocrine Related Cancer · doi:10.1530/erc-17-0416 · Cited by 25
Androgen receptor in salivary gland carcinoma: A review of an old marker as a possible new target
Yeoh, C. C., Dabab, N., Rigby, E., Chhikara, R., Akaev, I., Gomez, R. S., Fonseca, F. P., Brennan, P. A., & Rahimi, S. (2018) · Journal of Oral Pathology and Medicine · doi:10.1111/jop.12741 · Cited by 26
Miyazawa, Y., Sekine, Y., Shimizu, N., Takezawa, Y., Nakamura, T., Miyao, T., Nakayama, H., Kurihara, S., Syuto, T., Nomura, M., et al. (2019) · The Prostate · doi:10.1002/pros.23865 · Cited by 23
Kafka, M., Mayr, F., Temml, V., Möller, G., Adamski, J., Hoefer, J., Schwaiger, S., Heidegger, I. M., Matuszczak, B., Schuster, D., et al. (2020) · Cancers · doi:10.3390/cancers12082092 · Cited by 26
Transcriptional mediators of treatment resistance in lethal prostate cancerPreprint
He, M. X., Cuoco, M. S., Crowdis, J. P., Bosma-Moody, A., Zhang, Z., Bi, K., Kanodia, A., Su, M.-J., Rodman, C., DelloStritto, L. K., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.19.998450 · Cited by 25
Androgen receptor antagonists: a patent review (2008 – 2011)
Mohler, M. L., Coss, C. C., Duke, C. B., Patil, S. A., Miller, D. D., & Dalton, J. T. (2012) · Expert Opinion on Therapeutic Patents · doi:10.1517/13543776.2012.682571 · Cited by 25
Singh, K. B., Ji, X., & Singh, S. V. (2018) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-18-0117 · Cited by 25
Khurana, N., Chandra, P. K., Kim, H., Abdel‐Mageed, A. B., Mondal, D., & Sikka, S. C. (2020) · Antioxidants · doi:10.3390/antiox9010068 · Cited by 24
Targeting the N-terminal domain of the androgen receptor: The effective approach in therapy of CRPC
Ji, Y., Zhang, R., Han, X., & Zhou, J. (2022) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2022.115077 · Cited by 24
Zhang, H., Qi, L., Cai, Y., & Gao, X. (2024) · Annals of Medicine · doi:10.1080/07853890.2024.2320301 · Cited by 24
From AR to c-Met: Androgen deprivation leads to a signaling pathway switch in prostate cancer cells
Liu, T., Mendes, D. E., & Berkman, C. E. (2013) · International Journal of Oncology · doi:10.3892/ijo.2013.2020 · Cited by 24
Androgen receptor footprint on the way to prostate cancer progression
Hodgson, M. C., Bowden, W. A., & Agoulnik, I. U. (2011) · World Journal of Urology · doi:10.1007/s00345-011-0743-7 · Cited by 24
New Hormonal Therapies for Castration-Resistant Prostate Cancer
Mostaghel, E. A., & Plymate, S. R. (2011) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/j.ecl.2011.05.013 · Cited by 26
Kato, H., Furuya, Y., Miyazawa, Y., Miyao, T., Syuto, T., NOMURA, M., Sekine, Y., Koike, H., Matsui, H., Shibata, Y., et al. (2016) · Anticancer Research · doi:10.21873/anticanres.11205 · Cited by 23
Dissecting the roles of the androgen receptor in prostate cancer from molecular perspectives
Hu, J., Wang, G., & Sun, T. (2017) · Tumor Biology · doi:10.1177/1010428317692259 · Cited by 25
Targeting AR Variant–Coactivator Interactions to Exploit Prostate Cancer Vulnerabilities
Magani, F., Peacock, S. O., Rice, M. A., Martinez, M. J., Greene, A. M., Magani, P. S., Lyles, R. D. Z., Weitz, J., & Burnstein, K. L. (2017) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-17-0280 · Cited by 25
Current strategies for targeting the activity of androgen receptor variants
Armstrong, C. M., & Gao, A. C. (2018) · Asian journal of urology · doi:10.1016/j.ajur.2018.07.003 · Cited by 26
Alves, I. T., Hartjes, T. A., McClellan, E., Hiltemann, S., Böttcher, R., Dits, N. F. J., Temanni, M.-R., Janssen, B. J., van Workum, W., van der Spek, P. J., et al. (2014) · Oncogene · doi:10.1038/onc.2013.591 · Cited by 25
Modulating the Activity of Androgen Receptor for Treating Breast Cancer
You, C., Tsoi, H., Man, E. P. S., Leung, M., & Khoo, U. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232315342 · Cited by 23
Lee, S.-M., Lee, J.-G., Yun, T.-H., Cho, J. H., & Kim, K. S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25021197 · Cited by 25
Androgen Receptor Modulators: A Marriage of Chemistry and Biology
McEwan, I. J. (2013) · Future Medicinal Chemistry · doi:10.4155/fmc.13.69 · Cited by 23
Targeting the androgen receptor in metastatic castrate-resistant prostate cancer: A review
Anantharaman, A., & Friedlander, T. W. (2015) · Urologic Oncology Seminars and Original Investigations · doi:10.1016/j.urolonc.2015.11.003 · Cited by 23
Sun, H., Mediwala, S. N., Szafran, A. T., Mancini, M. A., & Marcelli, M. (2016) · Hormones and Cancer · doi:10.1007/s12672-016-0257-2 · Cited by 23
Streicher, W., Zengerling, F., Laschak, M., Weidemann, W. M., Höpfner, M., Schrader, A. J., Jentzmik, F., Schrader, M. G., & Cronauer, M. V. (2012) · World Journal of Urology · doi:10.1007/s00345-012-0842-0 · Cited by 25
Urbanucci, A., Marttila, S., Jänne, O. A., & Visakorpi, T. (2011) · The Prostate · doi:10.1002/pros.22473 · Cited by 22
Mellado, B., Jiménez, N., Marín‐Aguilera, M., & Reig, Ò. (2015) · Clinical Genitourinary Cancer · doi:10.1016/j.clgc.2015.12.030 · Cited by 22
Coordinated AR and microRNA regulation in prostate cancer
Eringyte, I., Losada, J. N. Z., Powell, S. M., Bevan, C. L., & Fletcher, C. E. (2020) · Asian journal of urology · doi:10.1016/j.ajur.2020.06.003 · Cited by 24
Sharma, U., Sahu, A., Shekhar, H., Sharma, B., Haque, S., Kaur, D., Tuli, H. S., Mishra, A., & Ahmad, F. (2025) · Discover Oncology · doi:10.1007/s12672-025-01829-4 · Cited by 21
Xu, P., Yang, J. C., Ning, S., Chen, B., Nip, C., Wei, Q., Liu, L., Johnson, O. T., Gao, A. C., Gestwicki, J. E., et al. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106692 · Cited by 24
Nuclear receptors and endobiotics glucuronidation: the good, the bad, and the UGT
Bigo, C., Caron, S., Dallaire-Théroux, A., & Barbier, O. (2013) · Drug Metabolism Reviews · doi:10.3109/03602532.2012.751992 · Cited by 21
Beyond Castration—Defining Future Directions in the Hormonal Treatment of Prostate Cancer
Niraula, S., Chi, K., & Joshua, A. M. (2011) · Hormones and Cancer · doi:10.1007/s12672-011-0096-0 · Cited by 21
Strategies for targeting the androgen receptor axis in prostate cancer
Carver, B. S. (2014) · Drug Discovery Today · doi:10.1016/j.drudis.2014.07.008 · Cited by 21
Chromatin reprogramming as an adaptation mechanism in advanced prostate cancer
Braadland, P. R., & Urbanucci, A. (2019) · Endocrine Related Cancer · doi:10.1530/erc-18-0579 · Cited by 21
Ma, T., Bai, S., Qi, Y., Zhan, Y., Ungerleider, N., Zhang, D. Y., Neklesa, T. K., Corey, E., Dehm, S. M., Zhang, K., et al. (2021) · Cancer Letters · doi:10.1016/j.canlet.2020.12.037 · Cited by 21
Androgen Receptor in Human Health: A Potential Therapeutic Target
Siddique, H. R., Nanda, S., Parray, A., & Saleem, M. (2012) · Current Drug Targets · doi:10.2174/138945012804545579 · Cited by 20
Tilki, D., & Evans, C. P. (2014) · PubMed · Cited by 20
Takeuchi, I., Takaha, N., Nakamura, T., Hongo, F., Mikami, K., Kamoi, K., Okihara, K., Kawauchi, A., & Miki, T. (2011) · The Prostate · doi:10.1002/pros.22460 · Cited by 19
Resveratrol enhances polyubiquitination-mediated ARV7 degradation in prostate cancer cells
Wilson, S., Cavero, L., Tong, D., Liu, Q., Geary, K. R., Talamonti, N., Xu, J., Fu, J., Jiang, J., & Zhang, D. (2017) · Oncotarget · doi:10.18632/oncotarget.18003 · Cited by 19
Molecular mechanisms of enzalutamide resistance in prostate cancer
Blatt, E. B., & Raj, G. V. (2019) · Cancer Drug Resistance · doi:10.20517/cdr.2019.25 · Cited by 19
Yu, B., Liu, Y., Luo, H., Fu, J., Yang, L., & Shao, C. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100276 · Cited by 18
Fiandalo, M. V., Wu, W., & Mohler, J. L. (2013) · Current Drug Targets · doi:10.2174/1389450111314040004 · Cited by 19
Mooney, S. M., Parsana, P., Hernandez, J. R., Liu, X., Verdone, J. E., Torga, G., Harberg, C. A., & Pienta, K. J. (2014) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24948 · Cited by 19
Azoitei, A., Merseburger, A. S., Godau, B., Hoda, M. R., Schmid, E., & Cronauer, M. V. (2016) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2016.06.008 · Cited by 20
Barsky, S. T., & Monks, D. A. (2025) · Biology of Sex Differences · doi:10.1186/s13293-025-00707-6 · Cited by 20
Thelen, P., Heinrich, E., Bremmer, F., Trojan, L., & Strauß, A. (2013) · The Prostate · doi:10.1002/pros.22711 · Cited by 18
Bedoya, D., & Mitsiades, N. (2011) · Expert Review of Anticancer Therapy · doi:10.1586/era.11.196 · Cited by 18
Ma, Y., Miao, Y., Peng, Z., Sandgren, J., de Ståhl, T. D., Huss, M., Lennartsson, L., Liu, Y., Nistér, M., Nilsson, S. F., et al. (2016) · SpringerPlus · doi:10.1186/s40064-016-3543-0 · Cited by 18
Performance comparison of two androgen receptor splice variant 7 (AR‐V7) detection methods
Bernemann, C., Steinestel, J., Humberg, V., Bögemann, M., Schrader, A. J., & Lennerz, J. K. (2018) · British Journal of Urology · doi:10.1111/bju.14146 · Cited by 17
Zhang, K., Firus, J., Prieur, B., Jia, W. W.-G., & Rennie, P. S. (2011) · Cancers · doi:10.3390/cancers3021498 · Cited by 18
Zengerling, F., Streicher, W., Schrader, A. J., Schrader, M. G., Nitzsche, B., Cronauer, M. V., & Höpfner, M. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms130911530 · Cited by 17
Potential molecular targeting of splice variants for cancer treatment.
Blair, C. A., & Zi, X. (2011) · PubMed · Cited by 17
Androgen receptor gene polymorphisms and alterations in prostate cancer: Of humanized mice and men
Robins, D. M. (2011) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2011.06.003 · Cited by 17
On the Origins of the Androgen Receptor Low Molecular Weight Species
Mudryj, M. M., & Tepper, C. G. (2013) · Hormones and Cancer · doi:10.1007/s12672-013-0152-z · Cited by 20
Chen, Y., & Lan, T. (2020) · Urologia Internationalis · doi:10.1159/000510124 · Cited by 17
RNA biomarkers to facilitate the identification of aggressive prostate cancer
Pellegrini, K. L., Sanda, M. G., & Moreno, C. S. (2015) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2015.05.003 · Cited by 17
Role of bromodomain and extraterminal (BET) proteins in prostate cancer
Mandl, A., Markowski, M. C., Carducci, M. A., & Antonarakis, E. S. (2023) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2023.2186851 · Cited by 16
Current uses and resistance mechanisms of enzalutamide in prostate cancer treatment
Miller, C. D., Likasitwatanakul, P., Toye, E., Hwang, J. H., & Antonarakis, E. S. (2024) · Expert Review of Anticancer Therapy · doi:10.1080/14737140.2024.2405103 · Cited by 15
Role of Signaling Transduction Pathways in Development of Castration-Resistant Prostate Cancer
Inoue, T., & Ogawa, O. (2011) · Prostate Cancer · doi:10.1155/2011/647987 · Cited by 16
Phase III data for abiraterone in an evolving landscape for castration-resistant prostate cancer
Pal, S. K., & Sartor, O. A. (2010) · Maturitas · doi:10.1016/j.maturitas.2010.10.009 · Cited by 16
Hattori, Y., Ishii, H., Munetomo, A., Watanabe, H., Morita, A., Sakuma, Y., & Ozawa, H. (2016) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.01.026 · Cited by 16
Precision medicine for prostate cancer
Galazi, M., Rodríguez‐Vida, A., Ng, T., MASON, M. D., & Chowdhury, S. (2014) · Expert Review of Anticancer Therapy · doi:10.1586/14737140.2014.972948 · Cited by 16
Androgen receptor isoforms expression in benign prostatic hyperplasia and primary prostate cancer
Hillebrand, A. C., Pizzolato, L. S., Neto, B. S., Branchini, G., & Brum, I. S. (2018) · PLoS ONE · doi:10.1371/journal.pone.0200613 · Cited by 17
Overcoming oncogene addiction in breast and prostate cancers: a comparative mechanistic overview
Blatt, E. B., Kopplin, N. G., Kumar, S., Mu, P., Conzen, S. D., & Raj, G. V. (2020) · Endocrine Related Cancer · doi:10.1530/erc-20-0272 · Cited by 15
Wüstmann, N., Seifert, K. E., Humberg, V., Vieler, J., Grundmann, N., Steinestel, J., Tiedje, D., Duensing, S. M., Krabbe, L., Bögemann, M., et al. (2023) · Biomarker Research · doi:10.1186/s40364-023-00481-w · Cited by 16
Functional implications and therapeutic targeting of androgen response elements in prostate cancer
Senapati, D., Sharma, V., Rath, S. K., Rai, U., & Panigrahi, N. (2023) · Biochimie · doi:10.1016/j.biochi.2023.07.012 · Cited by 15
Emerging role of miRNA in prostate cancer: A future era of diagnostic and therapeutics
Khan, M. M., Sharma, V., & Serajuddin, M. (2023) · Gene · doi:10.1016/j.gene.2023.147761 · Cited by 16
Therapeutic Approaches to Targeting Androgen Receptor Splice Variants
Daniels, V. A., Luo, J., Paller, C. J., & Kanayama, M. (2024) · Cells · doi:10.3390/cells13010104 · Cited by 16
Shukla, N., Shah, K., Rathore, D., Soni, K., Shah, J., Vora, H., & Dave, H. V. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.122697 · Cited by 15
Castration-resistant prostate cancer: potential targets and therapies
Saleem, M., Siddique, H. R., Konety, B. R., Nanda, S., & Parray (2012) · Biologics · doi:10.2147/btt.s23954 · Cited by 15
Overcoming castration resistance in prostate cancer
Tsao, C., Small, A., Galsky, M. D., & Oh, W. K. (2012) · Current Opinion in Urology · doi:10.1097/mou.0b013e3283523b8b · Cited by 15
Liu, W., Wang, C., Wang, S., Zeng, K., Wei, S., Sun, N., Sun, G., Wang, M., Zou, R., Liu, W., et al. (2020) · International Journal of Biological Sciences · doi:10.7150/ijbs.50810 · Cited by 15
Tsai, H.-C., Boucher, D. L., Martinez, A. D., Tepper, C. G., & Kung, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049887 · Cited by 16
Nakata, D., Nakayama, K., Masaki, T., Tanaka, A., Kusaka, M., & Watanabe, T. (2016) · The Prostate · doi:10.1002/pros.23238 · Cited by 14
The Genetic Complexity of Prostate Cancer
Compérat, É., Wasinger, G., Oszwald, A., Kain, R., Cancel‐Tassin, G., & Cussenot, O. (2020) · Genes · doi:10.3390/genes11121396 · Cited by 14
Laccetti, A. L., Morris, M. J., & Kantoff, P. W. (2020) · OncoTargets and Therapy · doi:10.2147/ott.s242921 · Cited by 16
Emerging therapies to overcome antiandrogen resistance and beyond in lethal prostate cancer
Huang, F., Li, K., Shevach, J. W., & Wang, Q. (2025) · Journal of the National Cancer Center · doi:10.1016/j.jncc.2025.04.004 · Cited by 18
Lessons from in-vivo models of castration-resistant prostate cancer
Lin, D., Gout, P. W., & Wang, Y. Z. (2013) · Current Opinion in Urology · doi:10.1097/mou.0b013e32835e9f07 · Cited by 14
Sequencing of agents for castration-resistant prostate cancer.
Hurwitz, M. E., & Petrylak, D. P. (2013) · PubMed · Cited by 14
Minges, J. T., Grossman, G., Zhang, P., Kafri, T., & Wilson, E. M. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.663641 · Cited by 15
Biomarker-Based Targeting of the Androgen-Androgen Receptor Axis in Advanced Prostate Cancer
Kohli, M., Qin, R., Jiménez, R. E., & Dehm, S. M. (2012) · Advances in Urology · doi:10.1155/2012/781459 · Cited by 14
Role of hormonal therapy for prostate cancer: perspective from Japanese experiences.
Namiki, M., Ueno, S., & Kitagawa, Y. (2012) · PubMed Central · doi:10.3978/j.issn.2223-4683.2012.07.03 · Cited by 15
Modulation of testosterone-dependent male sexual behavior and the associated neuroplasticity
Charlier, T. D., Seredynski, A. L., Niessen, N., & Balthazart, J. (2013) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2013.03.003 · Cited by 14
Expression of β-catenin and Mesenchymal Markers in Canine Prostatic Hyperplasia and Carcinoma
Lean, F. Z. X., Kontos, S., & Palmieri, C. (2014) · Journal of Comparative Pathology · doi:10.1016/j.jcpa.2013.12.008 · Cited by 14
McCarty, M. F., Hejazi, J., & Rastmanesh, R. (2014) · Integrative Cancer Therapies · doi:10.1177/1534735414534728 · Cited by 14
Martinez‐Ariza, G., & Hulme, C. (2015) · Pharmaceutical Patent Analyst · doi:10.4155/ppa.15.20 · Cited by 14
Metadata
- Authors
- Watson, P. A., Chen, Y. F., Balbas, M. D., Wongvipat, J., Socci, N. D., Viale, A., Kim, K., & Sawyers, C. L.
- Affiliations
- Memorial Sloan Kettering Cancer Center (US)
- Human Oncology and Pathogenesis Program,
- Bioinformatics Core,
- University of California, Los Angeles (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Sawyers, Charles L.
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2010-09-07
- Volume
- 107
- Issue
- 39
- Pages
- 16759-16765
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC2947883
- OpenAlex
- W2083926838
- Cited by
- 639
- References
- 27
- Citations by year
- 2026: 8 · 2025: 19 · 2024: 22 · 2023: 33 · 2022: 25 · 2021: 26 · 2020: 43 · 2019: 33 · 2018: 36 · 2017: 43 · 2016: 63 · 2015: 48 · 2014: 64 · 2013: 65 · 2012: 53
- FWCI
- 46.52
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Howard Hughes Medical Institute
- Prostate Cancer Foundation
- University of Washington
- National Cancer Institute
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Prostate Cancer Treatment and Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
- Keywords
- androgen receptor splice variants, castration-resistant prostate cancer, AR-V7, ligand-independent receptor activation, full-length androgen receptor, androgen withdrawal, antiandrogen resistance, enzalutamide, anchorage-independent growth, siRNA knockdown, prostate cancer cell lines, androgen receptor isoforms
- MeSH terms
- Amino Acid Sequence, Androgens, Animals, Castration, Disease Models, Animal, Exons, Humans, Male, Molecular Sequence Data, Prostatic Neoplasms, Receptors, Androgen, RNA, Messenger, Gene Expression Regulation, Neoplastic, Alternative Splicing, Protein Structure, Tertiary, Sequence Analysis, Protein, Cell Line, Tumor, Mice, Androgen Receptor Antagonists
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