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Distinct structural classes of activating FOXA1 alterations in advanced prostate cancer
Open accessAbstract
Abtract Forkhead box A1 (FOXA1) is a pioneer transcription factor that is essential for the normal development of several endoderm-derived organs, including the prostate gland 1,2. FOXA1 is frequently mutated in hormone-receptor-driven prostate, breast, bladder and salivary-gland tumours 3-8. However, it is unclear how FOXA1 alterations affect the development of cancer, and FOXA1 has previously been ascribed both tumour-suppressive 9-11 and oncogenic 12-14 roles. Here we assemble an aggregate cohort of 1,546 prostate cancers and show that FOXA1 alterations fall into three structural classes that diverge in clinical incidence and genetic co-alteration profiles, with a collective prevalence of 35%. Class-1 activating mutations originate in early prostate cancer without alterations in ETS or SPOP, selectively recur within the wing-2 region of the DNA-binding forkhead domain, enable enhanced chromatin mobility and binding frequency, and strongly transactivate a luminal androgen-receptor program of prostate oncogenesis. By contrast, class-2 activating mutations are acquired in metastatic prostate cancers, truncate the C-terminal domain of FOXA1, enable dominant chromatin binding by increasing DNA affinity and-through TLE3 inactivation-promote metastasis driven by the WNT pathway. Finally, class-3 genomic rearrangements are enriched in metastatic prostate cancers, consist of duplications and translocations within the FOXA1 locus, and structurally reposition a conserved regulatory element-herein denoted FOXA1 mastermind (FOXMIND)-to drive overexpression of FOXA1 or other oncogenes. Our study reaffirms the central role of FOXA1 in mediating oncogenesis driven by the androgen receptor, and provides mechanistic insights into how the classes of FOXA1 alteration promote the initiation and/or metastatic progression of prostate cancer. These results have direct implications for understanding the pathobiology of other hormone-receptor-driven cancers and rationalize the co-targeting of FOXA1 activity in therapeutic strategies.
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“many key genes that drive PCa, such as FOXA1 or HOXB13 (refs. 7,8), promote tumor progression by regulating how AR binds to or activates its target genes.”
From Genome-scale CRISPR screens identify PTGES3 as a direct modulator of androgen receptor function in advanced prostate cancer (2025) · cites this paper as [8]
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Cites
Robinson, M. D., McCarthy, D. J., & Smyth, G. K. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btp616 · Cited by 41,364
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
Liao, Y., Smyth, G. K., & Shi, W. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btt656 · Cited by 27,219
Cerami, E., Gao, J., Dogrusoz, U., Gross, B. E., Sumer, S. O., Aksoy, B. A., Jacobsen, A., Byrne, C. J., Heuer, M. L., Larsson, E., et al. (2012) · Cancer Discovery · doi:10.1158/2159-8290.cd-12-0095 · Cited by 17,455
The Molecular Signatures Database Hallmark Gene Set Collection
Liberzon, A., Birger, C., Thorvaldsdóttir, H., Ghandi, M., Mesirov, J. P., & Tamayo, P. (2015) · Cell Systems · doi:10.1016/j.cels.2015.12.004 · Cited by 13,807
Heinz, S., Benner, C., Spann, N., Bertolino, E., Lin, Y. C., Laslo, P., Cheng, J. X., Murre, C., Singh, H., & Glass, C. K. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.05.004 · Cited by 13,382
Comprehensive molecular portraits of human breast tumours
The Cancer Genome Atlas Network (2012) · Nature · doi:10.1038/nature11412 · Cited by 12,129
MEME SUITE: tools for motif discovery and searching
Bailey, T. L., Boden, M., Buske, F. A., Frith, M., Grant, C. E., Clementi, L., Ren, J., Li, W. W., & Noble, W. S. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp335 · Cited by 10,648
deepTools2: a next generation web server for deep-sequencing data analysis
Ramírez, F., Ryan, D. P., Grüning, B., Bhardwaj, V., Kilpert, F., Richter, A. S., Heyne, S., Dündar, F., & Manke, T. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw257 · Cited by 8,096
Buenrostro, J. D., Giresi, P. G., Zaba, L. C., Chang, H. Y., & Greenleaf, W. J. (2013) · Nature Methods · doi:10.1038/nmeth.2688 · Cited by 6,422
voom: precision weights unlock linear model analysis tools for RNA-seq read counts
Law, C. W., Chen, Y., Shi, W., & Smyth, G. K. (2014) · Genome Biology · doi:10.1186/gb-2014-15-2-r29 · Cited by 6,155
Research works printed but not linked: 1
- Smyth, G. K., McCarthy, D. J. & Smyth, G. K. in Bioinformatics and Computational Biology Solutions Using R and Bioconductor (eds Dudoit, S. & Carey, V. J.) 397–420 (Springer, New York, 2005).
Cited by
Sorted by citations
Items 101–200 of 284
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Feng, W., Ladewig, E., Lange, M., Salsabeel, N., Zhao, H., Lee, Y. S., Gopalan, A., Luo, H., Kang, W., Fan, N., et al. (2025) · Nature Genetics · doi:10.1038/s41588-025-02289-w · Cited by 25
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Su, Y., Zhang, Y., Zhao, J., Zhou, W., Wang, W., Han, B., & Wang, X. (2021) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-021-03730-3 · Cited by 22
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Mai, C., Chin, K., Foong, L. C., Pang, K.-L., Yu, B., Shu, Y., Chen, S., Cheong, S., & Chua, C. W. (2022) · Cancer Letters · doi:10.1016/j.canlet.2022.215794 · Cited by 22
Kodgule, R., Goldman, J. W., Monovich, A. C., Saari, T. W., Aguilar, A. R., Hall, C. N., Rajesh, N., Gupta, J., Chu, A., Ye, L., et al. (2022) · Blood Cancer Discovery · doi:10.1158/2643-3230.bcd-21-0224 · Cited by 29
Self-citationKneppers, J., Severson, T., Siefert, J. C., Schol, P. J., Joosten, S. E. P., Yu, I. P. L., Huang, C.-C. F., Morova, T., Altıntaş, U. B., Giambartolomei, C., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-35135-2 · Cited by 22
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Zucker, M., Perry, M., Gould, S. I., Elkrief, A., Safonov, A. M., Thummalapalli, R., Mehine, M. M., Chakravarty, D., Brannon, A. R., Ladanyi, M., et al. (2024) · Cell · doi:10.1016/j.cell.2024.11.010 · Cited by 19
Soundararajan, R., Viscuse, P. V., Pilie, P. G., Liu, J., Logotheti, S., Laberiano-Fernández, C., Lorenzini, D., Hoang, A. G., Lü, W., Soto, L. M. S., et al. (2022) · Cancers · doi:10.3390/cancers14133233 · Cited by 21
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Sumiyoshi, T., Chi, K. N., & Wyatt, A. W. (2021) · Prostate Cancer and Prostatic Diseases · doi:10.1038/s41391-020-00308-x · Cited by 21
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Hawley, J. R., Zhou, S., Arlidge, C., Grillo, G., Kron, K. J., Hugh-White, R., van der Kwast, T. H., Fraser, M. E., Boutros, P. C., Bristow, R. G., et al. (2021) · Cancer Research · doi:10.1158/0008-5472.can-21-2056 · Cited by 21
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Angappulige, D. H., Mahajan, N. P., & Mahajan, K. N. (2024) · Trends in cancer · doi:10.1016/j.trecan.2024.01.004 · Cited by 21
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Jillson, L. K., Yette, G. A., Laajala, T. D., Tilley, W. D., Costello, J. C., & Cramer, S. D. (2021) · Cancers · doi:10.3390/cancers13133272 · Cited by 20
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Clermont, P. (2023) · Epigenomics · doi:10.2217/epi-2023-0045 · Cited by 19
Li, J., Zhang, Y., Wang, L., Li, M., Yang, J., Chen, P., Zhu, J., Li, X., Zeng, Z., Li, G., et al. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05150-8 · Cited by 19
Self-citationSingh, R., Meng, H., Shen, T., Lumahan, L. E. V., Nguyen, S., Shen, H., Dasgupta, S., Qin, L., Karri, D., Zhu, B., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2218229120 · Cited by 19
Buskin, A., Singh, P., Lorenz, O., Robson, C. N., Strand, D. W., & Heer, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222313097 · Cited by 24
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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
Zhang, S., Zhang, H., Li, H., Guo, J., Wang, J., & Zhang, L. (2021) · Aging · doi:10.18632/aging.202604 · Cited by 16
Hu, L., Chen, X., Narwade, N. P., Lim, M. G. L., Chen, Z., Tennakoon, C., Guan, P., Chan, U. I., Zhao, Z., Deng, M., et al. (2021) · Oncogene · doi:10.1038/s41388-021-02026-7 · Cited by 16
Warren, I., Moeller, M. M., Guiggey, D., Chiang, A., Maloy, M. H., Ogoke, O., Groth, T., Mon, T., Meamardoost, S., Liu, X., et al. (2022) · The FASEB Journal · doi:10.1096/fj.202101506rrr · Cited by 17
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Zhang, X., Zhang, X., Deng, X., Cao, J., Bao, Q., Wang, H., Chen, D., & Tang, H. (2025) · International Journal of Surgery · doi:10.1097/js9.0000000000002611 · Cited by 15
Chukhu, M., Dahiya, U. R., & Heemers, H. V. (2025) · Oncogene · doi:10.1038/s41388-025-03573-z · Cited by 17
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Leach, D. A., Fernandes, R. C., & Bevan, C. L. (2022) · Endocrine Oncology · doi:10.1530/eo-22-0065 · Cited by 16
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Wang, Z., Petricca, J., Liu, M., Zhang, S., Chen, S., Li, M., Besschetnova, A., Patalano, S. C., Venkataramani, K., Siegfried, K. R., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2220472120 · Cited by 15
Mumphrey, M. B., Hosseini, N., Parolia, A., Geng, J., Zou, W., Raghavan, M., Chinnaiyan, A. M., & Cieslik, M. P. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112965 · Cited by 15
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Zhou, J., Cattoglio, C., Shao, Y., Tirumala, H. P., Vetralla, C., Bajikar, S. S., Li, Y., Chen, H., Wang, Q., Wu, Z., et al. (2023) · Genes & Development · doi:10.1101/gad.350733.123 · Cited by 15
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Shen, M., Demers, L.-K., Bailey, S. D., & Labbé, D. P. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.963007 · Cited by 15
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Bao, Y., Chang, Y., Tien, J. C.-Y., Cruz, G., Yang, F., Mannan, R., Mahapatra, S., Paturu, R., Cao, X., Su, F., et al. (2025) · Journal of Clinical Investigation · doi:10.1172/jci193745 · Cited by 13
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Cai, H., Agersnap, S. N., Sjøgren, A., Simonsen, M. K., Blaavand, M. S., Jensen, U. V., & Thomsen, M. K. (2022) · Cancers · doi:10.3390/cancers14184381 · Cited by 13
Hwang, J., Likasitwatanakul, P., Deshmukh, S. K., Wu, S., Kwon, J. J., Toye, E., Moline, D., Evans, M. G., Elliott, A., Passow, R., et al. (2025) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-24-3471 · Cited by 12
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Wang, T., Song, J., Qu, M., Gao, X., Zhang, W., Wang, Z., Zhao, L., Wang, Y., Li, B., Li, J., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.723676 · Cited by 12
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Self-citationXiang, R. R., Lee, S.-A., Tyndall, C. F., Bhatia, A. R., Yin, J., Singler, C., Hauk, B. J., Kipp, M. P., & Takeda, D. Y. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115312 · Cited by 11
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Zhang, Y.-W., Ma, J., Shi, C.-T., Han, W., Gao, X., Zhou, M.-H., Ding, H.-Z., & Wang, H. (2020) · Current Problems in Cancer · doi:10.1016/j.currproblcancer.2020.100559 · Cited by 11
Self-citationMachado, C. B., da Cunha, L. S., Maués, J. H. D. S., Pessoa, F. M. C. D. P., de Oliveira, M. B., Ribeiro, R. M., Lopes, G. S., de Moraes, M. O., de Moraes, M. E. A., Khayat, A. S., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105486 · Cited by 13
Li, H., Melnyk, J. E., Fu, B. X. H., Shrestha, R., Zhang, M., Sjöström, M., Feng, S., Anderson, J. A., Han, W., Chesner, L. N., et al. (2025) · Nature Genetics · doi:10.1038/s41588-025-02388-8 · Cited by 10
Self-citationHuttunen, J., Aaltonen, N., Helminen, L., Rilla, K. J., & Paakinaho, V. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05209-z · Cited by 10
Fenton, S. E., VanderWeeler, D. J., Rebbeck, T. R., & Chen, D. L. (2024) · American Society of Clinical Oncology Educational Book · doi:10.1200/edbk_433138 · Cited by 12
Goglia, A. G., Alshalalfa, M., Khan, A., Isakov, D., Hougen, H. Y., Swami, N. S., Kannikal, J., McBride, S. M., Gomez, D. R., Punnen, S., et al. (2024) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djae224 · Cited by 10
Ge, J., Liu, Y., Chen, P., Zeng, Z., Li, G., Xiong, W., Yi, M., & Xiang, B. (2024) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2024-010091 · Cited by 10
Choi, H. I., An, G. Y., Yoo, E., Baek, M., Binas, B., Chai, J. C., Lee, Y. S., Jung, K. H., & Chai, Y. G. (2022) · Scientific Reports · doi:10.1038/s41598-022-11868-4 · Cited by 10
Abouhashem, N. S., Harb, O. A., Elwan, A., Zaitoun, M., & Saraya, Y. S. (2022) · Polish Journal of Pathology · doi:10.5114/pjp.2022.120097 · Cited by 10
Zhang, H., & Zheng, Y. (2023) · Oncology Letters · doi:10.3892/ol.2023.13720 · Cited by 10
Hwang, K. W., Yun, J. W., & Kim, H. S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242115823 · Cited by 12
Hennessey, R. C., & Brown, K. M. (2021) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2020.11.010 · Cited by 10
Lehrer, S. P., & Rheinstein, P. H. (2020) · PubMed · Cited by 10
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Wen, X., Ding, T., Li, F., Fan, J., Fan, X., Jia, R., & Zhang, H. (2022) · Communications Biology · doi:10.1038/s42003-022-04007-2 · Cited by 10
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Gao, B. X., Xie, W., Wu, X., Wang, L., & Guo, J. (2020) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2020.188365 · Cited by 9
Yu, W., Zhang, T., Wang, B., Pan, J. G., Jin, S., Fang, B., Gu, W., Qin, X., Dai, B., Lin, G., et al. (2023) · Molecular Oncology · doi:10.1002/1878-0261.13511 · Cited by 9
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Liu, Z., Wang, Y., Aizimuaji, Z., Ma, S., & Xiao, T. (2022) · Disease Markers · doi:10.1155/2022/3317315 · Cited by 9
Malinczak, C., Fonseca, W., Mire, M. M., Parolia, A., Chinnaiyan, A. M., Rasky, A. J., Morris, S. B., Yagi, K., Bermick, J., & Lukacs, N. W. (2023) · Mucosal Immunology · doi:10.1016/j.mucimm.2023.06.002 · Cited by 9
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Cussenot, O., Cancel‐Tassin, G., Rao, S. R., Woodcock, D. J., Lamb, A. D. G., Mills, I. G., & Hamdy, F. C. (2023) · British Journal of Urology · doi:10.1111/bju.16120 · Cited by 10
Wang, Y., Li, L., Hao, M., Fu, D., Chen, J., Zhou, C., Fu, J., Yao, B., Chang, B., & Zhao, P. (2020) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2020.115160 · Cited by 9
Han, D. G., Owiredu, J. N., Healy, B. M., Li, M., Labaf, M., Steinfeld, J. S., Patalano, S. C., Gao, S., Liu, M., Macoska, J. A., et al. (2021) · Cancer Research · doi:10.1158/0008-5472.can-20-3042 · Cited by 9
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Uusi-Mäkelä, J., Afyounian, E., Tabaro, F., Häkkinen, T., Lussana, A., Shcherban, A., Annala, M., Nurminen, R., Kivinummi, K. K., Tammela, T. L. J., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.08.287268 · Cited by 11
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Broderick, A. J., Pan, E., Li, J., Chu, A., Hwang, C., Barata, P. C., Cackowski, F. C., Labriola, M., Ghose, A., Bilen, M. A., et al. (2024) · Prostate Cancer and Prostatic Diseases · doi:10.1038/s41391-024-00869-1 · Cited by 7
Lu, Z., Xiao, X., Zheng, Q., Wang, X., & Xu, L. (2024) · Briefings in Bioinformatics · doi:10.1093/bib/bbae366 · Cited by 7
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Tian, J., Chi, C., Bian, G., Guo, F., Wang, X., & Yu, B. (2020) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.13499 · Cited by 7
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Lee, J., & Lee, Y. (2025) · Molecules and Cells · doi:10.1016/j.mocell.2025.100193 · Cited by 7
Shuai, Y., & Huang, H. (2025) · Journal of the National Cancer Center · doi:10.1016/j.jncc.2025.06.001 · Cited by 6
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Formaggio, N., Sgrignani, J., Thillaiyampalam, G., Lorenzi, C., Cassanmagnago, G. A., Coazzoli, M., Costanzo, F., Uebelhart, Y., Bossi, D., Cassiano, D. C., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116324 · Cited by 6
Kneppers, J., Bergman, A. M., & Zwart, W. T. (2022) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-11836-4_15 · Cited by 6
Characterization of Wnt Signaling Pathway Aberrations in Metastatic Prostate Cancer
Choi, S. H., Pan, E., Elliott, A., Beltran, H., Panian, J. A., Jamieson, C. A. M., Bagrodia, A., Rose, B. S., Herchenhorn, D., Heath, E. I., et al. (2024) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-24-0395 · Cited by 6
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Gómora‐García, J. C., & Furlan-Magaril, M. (2025) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2025.102480 · Cited by 7
Eteleeb, A. M., Quigley, D. A., Zhao, S. G., Pham, D., Yang, R., Dehm, S. M., Luo, J. R., Feng, F. Y.-C., Dang, H. X., & Maher, C. A. (2020) · Scientific Reports · doi:10.1038/s41598-020-71168-7 · Cited by 6
Self-citationSheta, H., hafez, A. A. E., Saif, M., Elsergany, A. R., emam, D. A., & Abdelrazik, M. M. (2021) · Pathologica · doi:10.32074/1591-951x-217 · Cited by 6
Tong, H., Chen, H., & Williams, C. (2022) · Viruses · doi:10.3390/v14040837 · Cited by 6
Wei, J., Yu, H., Liu, T., Wang, Z., Lang, C., & Pan, Y. (2023) · Thoracic Cancer · doi:10.1111/1759-7714.14986 · Cited by 6
Hong, Z., Xu, C., Zheng, S., Wang, X., Tao, Y., Tan, Y., Lin, G., Wu, D., & Ye, D. (2023) · Cell Death Discovery · doi:10.1038/s41420-023-01682-w · Cited by 7
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Jiang, H., & Li, G. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1234515 · Cited by 5
Zhang, C., Jia, Y., & Kong, Q. (2023) · Pathology & Oncology Research · doi:10.3389/pore.2023.1611343 · Cited by 5
Budreika, A., Phoenix, J. T., Kostlan, R. J., Deegan, C. D., Ferrari, M. G., Young, K., Fanning, S., & Kregel, S. (2025) · Cancers · doi:10.3390/cancers17020306 · Cited by 4
Kim, J., Hwang, K. W., Lee, H. J., & Kim, H. S. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12111818 · Cited by 5
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Anstine, L. J., Majmudar, P. R., Aponte, A., Singh, S., Zhao, R., Weber-Bonk, K. L., Abdul‐Karim, F. W., Valentine, M. J., Seachrist, D. D., Grennel-Nickelson, K. E., et al. (2023) · Cancer Research · doi:10.1158/0008-5472.can-22-3133 · Cited by 5
Huang, R., Bornman, R. M. S., Stricker, P. D., Brum, I. S., Mutambirwa, S. B. A., Jaratlerdsiri, W., & Hayes, V. M. (2024) · Scientific Reports · doi:10.1038/s41598-024-57566-1 · Cited by 5
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Wyatt, A. W., & Vandekerkhove, G. R. (2020) · Société Internationale d’Urologie Journal · doi:10.48083/vsoo5322 · Cited by 5
Tang, F., Wang, S., Wong, C. K., Lee, C. J., Cohen, S. M., Park, J., Hill, C. E., Eng, K., Bareja, R., Han, T., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.26.355925 · Cited by 4
Felice, D. D., Alaimo, A., Bressan, D., Genovesi, S., Marmocchi, E., Annesi, N., Beccaceci, G., Dalfovo, D., Cutrupi, F., Medaglia, S., et al. (2024) · EMBO Reports · doi:10.1038/s44319-024-00335-y · Cited by 4
Phase Separation in Chromatin Organization and Human Diseases
Zhai, Z., Meng, F., Kuang, J., & Pei, D. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26115156 · Cited by 4
Liang, L., Dong, D., Sun, J., Zhang, Q., Yang, X., Zhang, P., & Wei, G.-H. (2025) · Cells · doi:10.3390/cells14131008 · Cited by 6
Hosseini, N., Mannan, R., Rebernick, R. J., Su, F., Wang, R., Cao, X., Lako, A., Mellacheruvu, D., Hu, J., Alumkal, J. J., et al. (2025) · Cancer Research · doi:10.1158/0008-5472.can-24-3687 · Cited by 5
Self-citation
Metadata
- Authors
- Parolia, A., Cieslik, M., Chu, S.-C., Xiao, L., Ouchi, T., Zhang, Y., Wang, X., Vats, P., Cao, X., Pitchiaya, S., Su, F., Wang, R., Feng, F. Y., Wu, Y.-M., Lonigro, R. J., Robinson, D. R., & Chinnaiyan, A. M.
- Affiliations
- University of Michigan (US)
- Howard Hughes Medical Institute (US)
- University of California, San Francisco (US)
- Corresponding author
- Chinnaiyan, Arul M.
- ORCID
- Venue
- Nature
- Published
- 2019-06-26
- Volume
- 571
- Issue
- 7765
- Pages
- 413-418
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC6661908
- OpenAlex
- W2955719861
- Cited by
- 284
- References
- 60
- Citations by year
- 2026: 25 · 2025: 40 · 2024: 34 · 2023: 44 · 2022: 47 · 2021: 50 · 2020: 35 · 2019: 9
- FWCI
- 25.92
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Cancer Institute (F99CA245825, R35CA231996, U01CA214170, P50CA186786)
- 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
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Genomics and Diagnostics
- Keywords
- FOXA1, prostate cancer, activating mutations, androgen receptor, chromatin binding, metastasis, Wnt signaling, TLE3, genome rearrangement, ETS transcription factors, SPOP, carcinogenesis
- MeSH terms
- Protein Domains, Chromatin, Humans, Male, Models, Molecular, Mutation, Neoplasm Metastasis, Prostatic Neoplasms, Receptors, Androgen, Genome, Human, Gene Expression Regulation, Neoplastic, Cell Line, Tumor, Hepatocyte Nuclear Factor 3-alpha, Wnt Signaling Pathway
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