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Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Open accessAbstract
Ependymomas are common childhood brain tumours that occur throughout the nervous system, but are most common in the paediatric hindbrain. Current standard therapy comprises surgery and radiation, but not cytotoxic chemotherapy as it does not further increase survival. Whole-genome and whole-exome sequencing of 47 hindbrain ependymomas reveals an extremely low mutation rate, and zero significant recurrent somatic single nucleotide variants. Although devoid of recurrent single nucleotide variants and focal copy number aberrations, poor-prognosis hindbrain ependymomas exhibit a CpG island methylator phenotype. Transcriptional silencing driven by CpG methylation converges exclusively on targets of the Polycomb repressive complex 2 which represses expression of differentiation genes through trimethylation of H3K27. CpG island methylator phenotype-positive hindbrain ependymomas are responsive to clinical drugs that target either DNA or H3K27 methylation both in vitro and in vivo. We conclude that epigenetic modifiers are the first rational therapeutic candidates for this deadly malignancy, which is epigenetically deregulated but genetically bland.
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Román‐Gómez, J., Jiménez‐Velasco, A., Agirre, X., Prósper, F., Heiniger, A., & Torres, A. (2005) · Journal of Clinical Oncology · doi:10.1200/jco.2005.01.4944 · Cited by 128
RetractedComprehensive molecular portraits of human breast tumours
The Cancer Genome Atlas Network (2012) · Nature · doi:10.1038/nature11412 · Cited by 12,129
Comprehensive molecular characterization of human colon and rectal cancer
The Cancer Genome Atlas Network (2012) · Nature · doi:10.1038/nature11252 · Cited by 8,499
Integrated genomic analyses of ovarian carcinoma
Perou, C. M. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/hvp3-wg08 · Cited by 7,927
Mutational heterogeneity in cancer and the search for new cancer-associated genes
Lawrence, M. S., Stojanov, P., Polak, P., Kryukov, G. V., Cibulskis, K., Sivachenko, A., Carter, S. L., Stewart, C., Mermel, C. H., Roberts, S. A., et al. (2013) · Nature · doi:10.1038/nature12213 · Cited by 5,461
Self-citationThe Somatic Genomic Landscape of Glioblastoma
Brennan, C. W., Verhaak, R. G. W., McKenna, A., Campos, B., Noushmehr, H., Salama, S. R., Zheng, S., Chakravarty, D., Sanborn, J. Z., Berman, S. H., et al. (2013) · Cell · doi:10.1016/j.cell.2013.09.034 · Cited by 5,016
Self-citationComprehensive genomic characterization of squamous cell lung cancers
The Cancer Genome Atlas Research Network (2012) · Nature · doi:10.1038/nature11404 · Cited by 3,994
Self-citationDriver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
Schwartzentruber, J., Korshunov, A., Liu, X.-Y., Jones, D. T. W., Pfaff, E., Jacob, K., Sturm, D., Fontebasso, A. M., Quang, D.-A. K., Tönjes, M., et al. (2012) · Nature · doi:10.1038/nature10833 · Cited by 2,631
Self-citationA landscape of driver mutations in melanoma
Hodis, E., Watson, I. R., Kryukov, G. V., Arold, S. T., Imielinski, M., Theurillat, J.-P., Nickerson, E., Auclair, D., Li, L., Place, C., et al. (2012) · Cell · doi:10.1016/j.cell.2012.06.024 · Cited by 2,610
Ben‐Porath, I., Thomson, M., Carey, V. J., Ge, R., Bell, G. W., Regev, A., & Weinberg, R. A. (2008) · Nature Genetics · doi:10.1038/ng.127 · Cited by 2,571
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Malhotra, A. K., Nobre, L. F., Ibrahim, G. M., Kulkarni, A. V., Drake, J. M., Rutka, J. T., Taylor, M. D., Ramaswamy, V., Dirks, P. B., & Dewan, M. C. (2024) · Journal of Neurosurgery Pediatrics · doi:10.3171/2023.11.peds23364 · Cited by 5
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Wang, B., Yan, M., Han, B. R., Liu, X., & Liu, P. (2024) · Neurosurgery · doi:10.1227/neu.0000000000002923 · Cited by 5
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Antoniades, E., Keffes, N., Vorri, S. C., Tsitouras, V., Gkantsinikoudis, N., Tsitsopoulos, P., & Magras, J. (2025) · Cancers · doi:10.3390/cancers17091566 · Cited by 5
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Self-citationPerruccio, K., Mastronuzzi, A., Lupattelli, M., Arcioni, F., Capolsini, I., Cerri, C., Gurdo, G., Massei, M. S., Mastrodicasa, E., & Caniglia, M. (2021) · Reports — Medical Cases Images and Videos · doi:10.3390/reports4020012 · Cited by 5
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Richterová, R., & Kolarovszki, B. (2018) · InTech eBooks · doi:10.5772/intechopen.74510 · Cited by 5
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Easwaran, H., & Baylin, S. B. (2019) · RNA technologies · doi:10.1007/978-3-030-14792-1_2 · Cited by 5
Cho, H. J., Park, H. Y., Kim, K., Chae, H., Paek, S. H., Kim, S., Park, C., Choi, S.-H., & Park, S. (2021) · Molecular and Clinical Oncology · doi:10.3892/mco.2021.2250 · Cited by 5
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Issa, J. J. (2017) · The Cancer Journal · doi:10.1097/ppo.0000000000000285 · Cited by 5
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Hamanishi, E. T., Dang, D., & Venneti, S. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1587157 · Cited by 4
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Self-citationCassim, A., Colino‐Sanguino, Y., Fox, S. L., de la Fuente, L. R., Hartley, H. E., & Valdés‐Mora, F. (2025) · Cancer and Metastasis Reviews · doi:10.1007/s10555-025-10284-0 · Cited by 8
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Self-citationBaibarac, M. A., Burlănescu, T., Stroe, M., Smaranda, I., & Negrila, C. C. (2022) · Polymers · doi:10.3390/polym14214479 · Cited by 4
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Wiehle, L., Raddatz, G., Pusch, S., Gutekunst, J., von Deimling, A., Rodríguez‐Paredes, M., & Lyko, F. (2017) · Cell Stress · doi:10.15698/cst2017.10.106 · Cited by 4
Davis, I. J., & Pattenden, S. G. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812433-8.00003-4 · Cited by 4
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Batchu, S., Patel, K., Yu, S., Mohamed, A. T., & Karsy, M. J. (2022) · Gene · doi:10.1016/j.gene.2022.146278 · Cited by 4
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Saxena, K., Subbalakshmi, A. R., Kulkarni, P., & Jolly, M. K. (2022) · Journal of Biosciences · doi:10.1007/s12038-022-00254-x · Cited by 4
Paparella, R., Caroleo, A. M., Agolini, E., Chillemi, G., Miele, E., Pedace, L., Rinelli, M., Pizzi, S., Boccuto, L., Colafati, G. S., et al. (2022) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.62869 · Cited by 4
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Xie, J., Lin, Y., Li, Y., Fang, A., Li, X., Wang, S., & Li, W. (2023) · Genes · doi:10.3390/genes14051052 · Cited by 4
Beekman, R., Kulis, M., & Martín-Subero, J. I. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800140-0.00009-1 · Cited by 4
de Sousa, G. R., Marie, S. K. N., Oba‐Shinjo, S. M., Ramalho, L. N. Z., Tone, L. G., & Valera, E. T. (2019) · Child s Nervous System · doi:10.1007/s00381-018-04028-5 · Cited by 4
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Arabzade, A., Stuckert, A. J., Bertrand, K. C., & Mack, S. C. (2020) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12612 · Cited by 4
Self-citationMaung, H. M. W., Chan-on, W., Kunkeaw, N., & Khaenam, P. (2019) · EXCLI journal · doi:10.17179/excli2019-1893 · Cited by 4
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Kline, C., Forester, C. M., & Banerjee, A. (2016) · Pediatric oncology · doi:10.1007/978-3-319-30789-3_4 · Cited by 4
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Xi, G., Mania-Farnell, B. L., Lei, T., & Tomita, T. (2016) · Oncology and Translational Medicine · doi:10.1007/s10330-016-0165-5 · Cited by 3
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Paik, S., Maule, F., & Gallo, M. (2020) · Genome · doi:10.1139/gen-2020-0097 · Cited by 5
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Cola, A. D., Foss, A., Gilbertson, R. J., & Pathania, M. (2023) · Annual Review of Cancer Biology · doi:10.1146/annurev-cancerbio-062722-034650 · Cited by 3
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Frappaz, D., Vasiljevic, A., Beuriat, P.-A., Alapetite, C., Grill, J., Szathmári, A., & Faure‐Conter, C. (2016) · Bulletin du Cancer · doi:10.1016/j.bulcan.2016.08.006 · Cited by 3
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Ibrahim, S., & Muhammad, F. (2020) · Nigerian Journal of Basic and Clinical Sciences. · doi:10.4103/njbcs.njbcs_2_20 · Cited by 3
Giangaspero, F., Minasi, S., Gianno, F., Alzoubi, H., Antonelli, M., & Buttarelli, F. R. (2020) · Glioma · doi:10.4103/glioma.glioma_20_20 · Cited by 3
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Turvey, G. L., de Alba, E. L., Stewart, E., Byrom, L., Cook, H., Sofi, S., Alalti, A., Ainscough, J., Mason, A. S., Antson, A. A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.22.558821 · Cited by 2
Ghalibafian, M., Mirzaei, S., Girinsky, T., Sadeghi, Y., Saffar, A., Ghodsinezhad, N., Elmi, S., & Bouffet, É. (2023) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2023.06.2294 · Cited by 2
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Montgomery, E. Y., Thirunavu, V. M., Pagadala, M. S., Shlobin, N. A., Plant, A., Lam, S. K., & DeCuypere, M. G. (2022) · Journal of Neurosurgery Pediatrics · doi:10.3171/2022.10.peds22154 · Cited by 2
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Huse, J. T., Abounader, R., Purow, B. W., Hegi, M. E., Soffietti, R., & Aldape, K. (2016) · Neuro-Oncology · doi:10.1093/neuonc/now215 · Cited by 2
Self-citationPersonalized Medicine Through Advanced Genomics
Youngblood, M. W., Erson-Omay, Z., & Günel, M. (2016) · Springer eBooks · doi:10.1007/978-3-319-49864-5_3 · Cited by 2
Transposase-driven rearrangements in human tumors
Mack, S. C., Suzuki, H., & Taylor, M. D. (2017) · Nature Genetics · doi:10.1038/ng.3908 · Cited by 2
Self-citationCancer research: quo vadis—to war?
Wheatley, D. N. (2014) · ecancermedicalscience · doi:10.3332/ecancer.2014.ed45 · Cited by 2
Recent Advancements in Ependymoma: Challenges and Therapeutic Opportunities
Bertrand, K. C., & Klimo, P. D. (2023) · Pediatric Neurosurgery · doi:10.1159/000530868 · Cited by 2
Self-citationDubuc, A. M., & Ligon, A. H. (2017) · Current Genetic Medicine Reports · doi:10.1007/s40142-017-0127-4 · Cited by 2
Self-citationToward an integrated histomolecular diagnosis of supratentorial ependymoma
Pajtler, K. W. (2016) · Neuro-Oncology · doi:10.1093/neuonc/now054 · Cited by 2
Kulasingam, V., & Diamandis, E. P. (2018) · The Journal of Applied Laboratory Medicine · doi:10.1373/jalm.2018.027557 · Cited by 1
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Chen, J., Keshavarzian, T., & Lupien, M. (2024) · Royal Society of Chemistry eBooks · doi:10.1039/9781837674916-00109 · Cited by 1
Self-citationBasic Science of Pediatric Brain Tumors
Taccone, M. S., Srikanthan, D., Rutka, J. T., & Ramaswamy, V. (2024) · Springer eBooks · doi:10.1007/978-3-031-62017-1_7 · Cited by 1
Self-citationProgress Toward Epigenetic Targeted Therapies for Childhood Cancer
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Shatara, M., Ho, W. S., Roland, J. L., & Limbrick, D. D. (2025) · Advances in cancer research · doi:10.1016/bs.acr.2025.09.004 · Cited by 1
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Paul, D. (2025) · Springer eBooks · doi:10.1007/978-3-032-08808-6_5 · Cited by 1
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Biswas, K., Ghosh, S., Khincha, P. P., Sundby, R. T., Singh, A., Ault, G. S., Henderson, M. J., Gross, A. M., Donoghue, M. B., Savage, S. A., et al. (2026) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djag068 · Cited by 1
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Lundstrom, K. H. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-420135-4.00013-9 · Cited by 1
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Lennartsson, A. (2016) · Genome biology · doi:10.1186/s13059-016-0884-5 · Cited by 1
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Fujii, C. F. H. (2015) · Journal of Carcinogenesis & Mutagenesis · doi:10.4172/2157-2518.1000209 · Cited by 1
Yang, Z., Jia, M., Liu, G., Hao, H., Chen, L., Li, G., Liu, S., Li, Y., Wu, C., Lu, X., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0187551 · Cited by 1
Gorsi, H. S., Toll, S. A., Sood, S., Miler, S., Altinok, D., Kumar‐Sinha, C., Mody, R., & Yankelevich, M. (2021) · Journal of Pediatric Hematology/Oncology · doi:10.1097/mph.0000000000002175 · Cited by 1
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Seno, A., Afify, S. M., Hassan, G., & Seno, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85545-7.00002-8 · Cited by 1
Pediatric posterior fossa ependymoma and metabolism
Halligan, K. E., Michealraj, K. A., Cruz, A. F., Felker, J. T., Daniels, C. E., Taylor, M. D., & Agnihotri, S. (2021) · Glioma · doi:10.4103/glioma.glioma_17_21 · Cited by 1
Self-citationVillar, R. C., & Merchant, T. E. (2018) · Pediatric oncology · doi:10.1007/978-3-319-43545-9_12 · Cited by 1
Witt, H., & Pajtler, K. W. (2018) · Springer eBooks · doi:10.1007/978-3-319-43205-2_8 · Cited by 1
Self-citationYiallouros, M. (2007) · doi:10.1591/poh.patinfo.ependy.kurz.1.20070626 · Cited by 1
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Self-citation
Metadata
- Authors
- Mack, S. C., Witt, H., Piro, R. M., Gu, L., Zuyderduyn, S., Stütz, A. M., Wang, X., Gallo, M., Garzia, L., Zayne, K., Zhang, X., Ramaswamy, V., Jäger, N., Jones, D. T. W., Sill, M., Pugh, T. J., Ryzhova, M., Wani, K. M., Shih, D. J. H., Head, R., Remke, M., Bailey, S. D., Zichner, T., Faria, C. C., Barszczyk, M., Stark, S., Seker-Cin, H., Hutter, S., Johann, P., Bender, S., Hovestadt, V., Tzaridis, T., Dubuc, A. M., Northcott, P. A., Peacock, J., Bertrand, K. C., Agnihotri, S., Cavalli, F. M. G., Clarke, I., Nethery-Brokx, K., Creasy, C. L., Verma, S. K., Koster, J., Wu, X., Yao, Y., Milde, T., Sin-Chan, P., Zuccaro, J., Lau, L., Pereira, S., Castelo-Branco, P., Hirst, M., Marra, M. A., Roberts, S. S., Fults, D., Massimi, L., Cho, Y. J., Van Meter, T., Grajkowska, W., Lach, B., Kulozik, A. E., von Deimling, A., Witt, O., Scherer, S. W., Fan, X., Muraszko, K. M., Kool, M., Pomeroy, S. L., Gupta, N., Phillips, J., Huang, A., Tabori, U., Hawkins, C., Malkin, D., Kongkham, P. N., Weiss, W. A., Jabado, N., Rutka, J. T., Bouffet, E., Korbel, J. O., Lupien, M., Aldape, K. D., Bader, G. D., Eils, R., Lichter, P., Dirks, P. B., Pfister, S. M., Korshunov, A., & Taylor, M. D.
- Affiliations
- University of Toronto (CA)
- German Cancer Research Center (DE)
- European Molecular Biology Laboratory (DE)
- Hospital for Sick Children (CA)
- Dartmouth–Hitchcock Medical Center (US)
- Boston Children's Hospital (US)
- The University of Texas MD Anderson Cancer Center (US)
- Ontario Institute for Cancer Research (CA)
- GlaxoSmithKline (United States) (US)
- BC Cancer Agency (CA)
- Uniformed Services University of the Health Sciences (US)
- University of Utah (US)
- Agostino Gemelli University Polyclinic (IT)
- Stanford Medicine (US)
- Children's Memorial Health Institute (PL)
- Hamilton General Hospital (CA)
- Heidelberg University (DE)
- University of Michigan (US)
- University of California, San Francisco (US)
- McGill University Health Centre (CA)
- Corresponding author
- Korshunov, A.
- Taylor, M. D.
- ORCID
- Mack, S. C.
- Witt, H.
- Piro, R. M.
- Gu, L.
- Stütz, A. M.
- Wang, X.
- Gallo, M.
- Garzia, L.
- Zhang, X.
- Ramaswamy, V.
- Jäger, N.
- Jones, D. T. W.
- Sill, M.
- Pugh, T. J.
- Ryzhova, M.
- Wani, K. M.
- Shih, D. J. H.
- Remke, M.
- Bailey, S. D.
- Zichner, T.
- Faria, C. C.
- Barszczyk, M.
- Hutter, S.
- Johann, P.
- Hovestadt, V.
- Tzaridis, T.
- Dubuc, A. M.
- Northcott, P. A.
- Bertrand, K. C.
- Agnihotri, S.
- Cavalli, F. M. G.
- Creasy, C. L.
- Verma, S. K.
- Wu, X.
- Yao, Y.
- Milde, T.
- Zuccaro, J.
- Lau, L.
- Pereira, S.
- Hirst, M.
- Marra, M. A.
- Roberts, S. S.
- Fults, D.
- Massimi, L.
- Cho, Y. J.
- Grajkowska, W.
- Lach, B.
- Kulozik, A. E.
- Witt, O.
- Scherer, S. W.
- Fan, X.
- Muraszko, K. M.
- Kool, M.
- Pomeroy, S. L.
- Gupta, N.
- Phillips, J.
- Huang, A.
- Tabori, U.
- Hawkins, C.
- Malkin, D.
- Kongkham, P. N.
- Weiss, W. A.
- Jabado, N.
- Rutka, J. T.
- Korbel, J. O.
- Lupien, M.
- Aldape, K. D.
- Bader, G. D.
- Eils, R.
- Lichter, P.
- Dirks, P. B.
- Pfister, S. M.
- Korshunov, A.
- Taylor, M. D.
- Venue
- Nature
- Published
- 2014-02
- Volume
- 506
- Issue
- 7489
- Pages
- 445-450
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4174313
- OpenAlex
- W2113432767
- Cited by
- 607
- References
- 50
- Citations by year
- 2026: 15 · 2025: 29 · 2024: 30 · 2023: 29 · 2022: 37 · 2021: 51 · 2020: 56 · 2019: 55 · 2018: 68 · 2017: 64 · 2016: 73 · 2015: 57 · 2014: 40
- FWCI
- 39.14
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Pure Amsterdam UMC (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Pediatric Brain Tumor Foundation
- CureSearch for Children's Cancer
- Deutsches Krebsforschungszentrum
- Government of Ontario
- Bundesministerium für Bildung und Forschung (01KU1201A, 01GS0883)
- Terry Fox Research Institute
- Deutsche Krebshilfe (109252)
- Deutschen Konsortium für Translationale Krebsforschung
- National Institutes of Health
- Canadian Institutes of Health Research
- National Cancer Institute (R01CA148699, R01CA148621, R01CA121941, R01CA163737, R01CA159859, P30CA016672, P50CA097257)
- Topics
- Health Sciences › Medicine › Oncology › Glioma Diagnosis and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- ependymoma, CpG island methylator phenotype, pediatric brain tumors, C11orf95-RELA fusion, chromothripsis, NF-κB signaling, H3K27me3, polycomb repressive complex 2, DNA methylation, EZH2 inhibitors, epigenetic therapy, tumor suppressor
- MeSH terms
- Animals, Brain Neoplasms, Ependymoma, Female, Histones, Humans, Infant, Mutation, Phenotype, Prognosis, Rhombencephalon, Gene Expression Regulation, Neoplastic, Mice, SCID, Mice, Inbred NOD, CpG Islands, DNA Methylation, Gene Silencing, Xenograft Model Antitumor Assays, Epigenesis, Genetic, Mice, Embryonic Stem Cells, Epigenomics, Polycomb Repressive Complex 2
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