The DOI matches its Crossref record; 46 of the 46 references it cites were found in a registry or an index.
A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells
Abstract
EZH2 catalyzes trimethylation of histone H3 lysine 27 (H3K27). Point mutations of EZH2 at Tyr641 and Ala677 occur in subpopulations of non-Hodgkin's lymphoma, where they drive H3K27 hypertrimethylation. Here we report the discovery of EPZ005687, a potent inhibitor of EZH2 (K(i) of 24 nM). EPZ005687 has greater than 500-fold selectivity against 15 other protein methyltransferases and has 50-fold selectivity against the closely related enzyme EZH1. The compound reduces H3K27 methylation in various lymphoma cells; this translates into apoptotic cell killing in heterozygous Tyr641 or Ala677 mutant cells, with minimal effects on the proliferation of wild-type cells. These data suggest that genetic alteration of EZH2 (for example, mutations at Tyr641 or Ala677) results in a critical dependency on enzymatic activity for proliferation (that is, the equivalent of oncogene addiction), thus portending the clinical use of EZH2 inhibitors for cancers in which EZH2 is genetically altered.
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
“More recently, the arginine methyltransferase PRMT5 has been implicated in driving neoplastic growth of multiple tumours including B cell lymphoma, multiple myeloma, breast cancer and glioblastoma 171-178 .”
From The roles of DNA, RNA and histone methylation in ageing and cancer (2019) · cites this paper as [173]
Citations
Cites
Improved survival with vemurafenib in melanoma with BRAF V600E mutation
Chapman, P. B., Hauschild, A., Robert, C., Haanen, J. B., Ascierto, P., Larkin, J., Dummer, R., Garbe, C., Testori, A., Maio, M., et al. (2011) · New England Journal of Medicine · doi:10.1056/nejmoa1103782 · Cited by 7,720
Anaplastic Lymphoma Kinase Inhibition in Non–Small-Cell Lung Cancer
Kwak, E. L., Bang, Y., Camidge, D. R., Shaw, A. T., Solomon, B., Maki, R. G., Ou, S. I., Dezube, B. J., Janne, P. A., Costa, D. B., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa1006448 · Cited by 4,477
Role of Histone H3 Lysine 27 Methylation in Polycomb-Group Silencing
Cao, R., Wang, L., Wang, H., Xia, L., Erdjument-Bromage, H., Tempst, P., Jones, R. S., & Zhang, Y. (2002) · Science · doi:10.1126/science.1076997 · Cited by 3,775
The polycomb group protein EZH2 is involved in progression of prostate cancer
Varambally, S., Dhanasekaran, S. M., Zhou, M., Barrette, T. R., Kumar-Sinha, C., Sanda, M. G., Ghosh, D., Pienta, K. J., Sewalt, R. G. A. B., Otte, A. P., et al. (2002) · Nature · doi:10.1038/nature01075 · Cited by 2,717
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
Morin, R. D., Johnson, N. A., Severson, T., Mungall, A. J. J., An, J., Goya, R., Paul, J. E., Boyle, M., Woolcock, B. W., Kuchenbauer, F. C., et al. (2010) · Nature Genetics · doi:10.1038/ng.518 · Cited by 1,719
Kleer, C. G., Cao, Q., Varambally, S., Shen, R., Ota, I., Tomlins, S. A., Ghosh, D., Sewalt, R. G. A. B., Otte, A. P., Hayes, D. F., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1933744100 · Cited by 1,649
Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma
Morin, R. D., Mendez-Lago, M., Mungall, A. J., Goya, R., Mungall, K. L., Corbett, R. D., Johnson, N. A., Severson, T. M., Chiu, R., Field, M., et al. (2011) · Nature · doi:10.1038/nature10351 · Cited by 1,614
Kuzmichev, A., Nishioka, K., Erdjument-Bromage, H., Tempst, P., & Reinberg, D. (2002) · Genes & Development · doi:10.1101/gad.1035902 · Cited by 1,596
UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development
Agger, K., Cloos, P. A., Christensen, J. F., Pasini, D., Rose, S., Rappsilber, J., Issaeva, I., Canaani, E., Salcini, A. E., & Helin, K. (2007) · Nature · doi:10.1038/nature06145 · Cited by 1,392
Flagged first, then by citations
Cited by
Sorted by citations
Items 601–700 of 807
Epimutations and Their Effect on Chromatin Organization: Exciting Avenues for Cancer Treatment
Mohammad, A., & Jha, S. (2022) · Cancers · doi:10.3390/cancers15010215 · Cited by 6
Benefits and Challenges of Inhibiting EZH2 in Malignant Pleural Mesothelioma
Khatib, M. O. A., Pinton, G., Moro, L., & Porta, C. (2023) · Cancers · doi:10.3390/cancers15051537 · Cited by 7
Simon, J. A. (2012) · Nature Chemical Biology · doi:10.1038/nchembio.1088 · Cited by 6
18F-Labeled PET Probe Targeting Enhancer of Zeste Homologue 2 (EZH2) for Cancer Imaging
Yu, L., Despotovic, N., Kovacs, M. S., Pin, C. L., & Luyt, L. G. (2019) · ACS Medicinal Chemistry Letters · doi:10.1021/acsmedchemlett.8b00613 · Cited by 6
Hong, F., Zhao, M., Zhang, L. J., & Feng, L. (2019) · Stem Cells and Development · doi:10.1089/scd.2018.0258 · Cited by 6
Carcinogenic roles and therapeutic effects of EZH2 in gynecological cancers
Wan, Z., Jiang, H., Li, L., Zhu, S., Hou, J., & Yu, Y. (2020) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2020.115379 · Cited by 6
NAKAYAMA, H., Kawachi, K., Suganuma, N., Yoshida, T., Yamashita, T., Yamanaka, T., Matsubara, Y., Kohagura, K., Toda, S., Nakamura, Y., et al. (2020) · Anticancer Research · doi:10.21873/anticanres.14172 · Cited by 6
Li, W., Liu, T., Wu, T., Cai, T., Wang, F. W., & Zhang, M. (2025) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2025.189492 · Cited by 5
Au cœur d’une complexité biologique
Koubi, M., Chabannon, C., & Duprez, E. (2017) · médecine/sciences · doi:10.1051/medsci/20173305013 · Cited by 5
Keilhack, H., & Chang, P. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6993-7_21 · Cited by 5
Self-citationGenetic Impairments of PRC2 Activity in Oncology: Problems and Prospects
Chetverina, D., Ломаев, Д. В., Georgiev, P. G., & Erokhin, M. (2021) · Russian Journal of Genetics · doi:10.1134/s1022795421030042 · Cited by 5
Hu, J., Xu, H., Ma, X., Bai, M., Zhou, Y., Miao, R., Wang, F., Li, X., & Cheng, B. (2024) · American Journal Of Pathology · doi:10.1016/j.ajpath.2024.03.012 · Cited by 5
EZH2: a potential new target in T-cell lymphoma?
Giulino-Roth, L. G. (2014) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.3109/10428194.2014.987770 · Cited by 5
Diagnostic and Therapeutic Implications of Histone Epigenetic Modulators in Breast Cancer
Walsh, L., Gallagher, W. M., O’Connor, D. P., & Chonghaile, T. N. (2016) · Expert Review of Molecular Diagnostics · doi:10.1586/14737159.2016.1156534 · Cited by 5
Bergamin, E., & Couture, J. F. (2016) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2016.01.004 · Cited by 5
Reynolds, V. L., Butler, P., Abernathy, M. M., Aschenbrenner, L. M., Best, D. D., Blank, J., Crosby, M. E., Custer, L. L., Escobar, P. A., Kolaja, K. L., et al. (2020) · Regulatory Toxicology and Pharmacology · doi:10.1016/j.yrtph.2020.104746 · Cited by 5
Comprehensive Assessment and Classification of High-Grade B-cell Lymphomas
Behdad, A., & Bailey, N. G. (2016) · Surgical pathology clinics · doi:10.1016/j.path.2015.09.008 · Cited by 5
Discovery and Development of Small Molecules Targeting Epigenetic Enzymes with Computational Methods
Meng, F., Wang, C., Wan, W., Lu, W., Lu, W., & Luo, C. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802808-7.00004-6 · Cited by 5
Danishuddin, M., Kumar, V., Parate, S., Bahuguna, A., Lee, G., Kim, M. O., & Lee, K. W. (2021) · Pharmaceuticals · doi:10.3390/ph14070699 · Cited by 5
Aberrant histone modifications in pediatric brain tumors
Hamanishi, E. T., Dang, D., & Venneti, S. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1587157 · Cited by 4
An updated patent review of EZH2 inhibitors (2024–present)
Wan, G., Li, S., Tang, Q., Qiu, H., Zhang, Q., & Yu, L. (2025) · Expert Opinion on Therapeutic Patents · doi:10.1080/13543776.2025.2483399 · Cited by 4
AURKA / PLK1 / CDC25C Axis as a Novel Therapeutic Target in INI1 ‐Deficient Epithelioid Sarcoma
Inoue, A., Outani, H., Imura, Y., Nakai, S., Takami, H., Kotani, Y., Mae, H., & Okada, S. (2025) · Cancer Science · doi:10.1111/cas.16438 · Cited by 4
Histone Methyltransferase Activity Assays
Ma, H., Howitz, K. T., Horiuchi, K. Y., & Wang, Y. (2015) · Royal Society of Chemistry eBooks · doi:10.1039/9781782628484-00267 · Cited by 3
Gene Transcription as a Therapeutic Target in Leukemia
Khamidullina, A. I., Varlamova, E. A., Hammoud, N. A., Yastrebova, M. A., & Bruter, A. V. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147340 · Cited by 4
Brasier, A. R. (2023) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2023.03.024 · Cited by 4
Childhood medulloblastoma: current and future treatment strategies
Hennika, T., & Gururangan, S. (2015) · Expert Opinion on Orphan Drugs · doi:10.1517/21678707.2015.1087311 · Cited by 4
Duncan, K. W., & Campbell, J. E. (2017) · Topics in medicinal chemistry · doi:10.1007/7355_2017_30 · Cited by 4
Epigenetic analysis in cancer research
Tyagi, L., Kumar, U., Mishra, S., Simran, S., Rathi, G., & Parashar, D. (2025) · Methods in cell biology · doi:10.1016/bs.mcb.2025.02.021 · Cited by 3
Abulkhair, H. S. (2026) · RSC Advances · doi:10.1039/d5ra08746e · Cited by 3
Epigenetic therapy gains momentum
Seton-Rogers, S. E. (2012) · Nature reviews. Cancer · doi:10.1038/nrc3402 · Cited by 3
Autophagic effect of SAM-competitive EZH2 inhibitors on cancer cells
(2015) · Cancer Cell & Microenvironment · doi:10.14800/ccm.551 · Cited by 3
Brown, R. E., Fuchter, M., Curry, E. W., Green, I. A., Kandil, S., Cherblanc, F., Payne, L., Chapman‐Rothe, N., Shamsaei, E., Srimongkolpithak, N., et al. (2014) · European Journal of Cancer · doi:10.1016/s0959-8049(14)70680-x · Cited by 3
Novel Drugs Targeting the Epigenome
Chen, Z., & Li, H. (2017) · Current Pharmacology Reports · doi:10.1007/s40495-017-0100-7 · Cited by 3
Histone methylation modifiers in medical therapeutics
Trojer, P. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823928-5.00020-7 · Cited by 3
Protein Lysine Methyltransferases Inhibitors
Li, Y., Ding, L., Ren, S., Zhang, W., & Rao, G. (2022) · Current Medicinal Chemistry · doi:10.2174/0929867329666220829151257 · Cited by 3
Epigenetic Factors: Key Regulators Targeted in Cancers
Yeo-Teh, N. S. L., Ito, Y., & Jha, S. (2018) · InTech eBooks · doi:10.5772/intechopen.73040 · Cited by 3
Pathobiology of pancreatic cancer: implications on therapy
Regel, I., Hausmann, S., Benitz, S., Esposito, I., & Kleeff, J. H. (2015) · Expert Review of Anticancer Therapy · doi:10.1586/14737140.2016.1129276 · Cited by 3
EZH2 Inhibitor GSK126: Metabolism, drug transporter and rat pharmacokinetic studies
Kumar, A., & Wempe, M. F. (2015) · Medical Research Archives · doi:10.18103/mra.v0i3.273 · Cited by 3
Riera, T. V., Wigle, T. J., & Copeland, R. A. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-3673-1_2 · Cited by 3
Self-citationMisregulation of Histone Methylation Regulators in Cancer
Ooi, W. F., Yao, X., Tan, P. B. O., & Teh, B. T. (2017) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-3-319-59786-7_8 · Cited by 3
Recent Advances in Chemical Tools for the Regulation and Study of Protein Lysine Methyltransferases
Hirano, T., Mori, S., & Kagechika, H. (2018) · The Chemical Record · doi:10.1002/tcr.201800034 · Cited by 3
Pathology and Molecular Pathogenesis of DLBCL and Related Entities
Pasqualucci, L., & Ott, G. (2018) · Methods in molecular biology · doi:10.1007/978-3-030-00362-3_2 · Cited by 4
Chromatin dynamics underlying latent responses to xenobiotics
Moggs, J. G., & Terranova, R. (2018) · Toxicology Research · doi:10.1039/c7tx00317j · Cited by 3
Li, P., Fujisawa, T., Narita, H., Uneme, Y., Seki, M., Hu, M., Narumi, R., Namekawa, S. H., Khan, S. S., Davie, J., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.24.625111 · Cited by 3
Derepressing of STAT3 and USP7 contributes to resistance of DLBCL to EZH2 inhibition
He, C., Zhou, W., Jin, X., & Zhou, H. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e20650 · Cited by 3
GSK343, an inhibitor of EZH2, prevents acquired cisplatin resistance in bladder cancer
He, L., & Liu, P. (2025) · Molecular Genetics and Genomics · doi:10.1007/s00438-025-02273-3 · Cited by 2
Chromatin Regulatory Targets for Anticancer Therapeutics
Barta, P. A., Carter, T. R., & Erb, M. A. (2025) · Chemical Reviews · doi:10.1021/acs.chemrev.5c00231 · Cited by 2
Omoboyowa, D. A., Aribigbola, T. C., Aiyeku, B., Bodun, D. S., & Oyeneyin, O. E. (2025) · Computational Biology and Chemistry · doi:10.1016/j.compbiolchem.2025.108784 · Cited by 2
Kim, A., Pan, B., Yu, X., Gao, X., Khudaverdyan, N., Taherian, F., Xu, C., Zhong, H., Xiong, Y., Kanıskan, H. Ü., et al. (2026) · Nature Cell Biology · doi:10.1038/s41556-026-02048-x · Cited by 2
Self-citationNew method for synthesis of EZH2 methyltransferase inhibitor GSK126
Lu, C. H., Zhang, Q., & Chen, X. (2016) · Synthetic Communications · doi:10.1080/00397911.2016.1193875 · Cited by 2
Activating Mutations of the EZH2 Histone Methyltransferase in Cancer
Kruger, R. G., Graves, A. P., & McCabe, M. T. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809737-3.00011-8 · Cited by 2
Small Molecule Inhibitors Targeting New Targets of Protein-Protein Interactions
Yue, L., Wan, W., Xu, P., Li, L., Wang, C., Zhang, Y., Xu, H., Zhang, R., Hu, J., Lu, W., et al. (2018) · Springer eBooks · doi:10.1007/978-981-13-0773-7_7 · Cited by 2
Mezey, N., Cho, W. C. S., & Biggar, K. K. (2019) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2019.03.005 · Cited by 2
Targeting the PRC2-dependent epigenetic program alleviates urinary tract infections
Guo, C., Zhao, M., Sui, X., Balsara, Z. R., Zhai, S., Ahdoot, M. A., Zhang, Y., Lam, C. M., Zhu, P., & Li, X. (2023) · iScience · doi:10.1016/j.isci.2023.106925 · Cited by 2
Polycomb Repressive Complex 2 in Oncology
Guo, Y., Yu, Y., & Wang, G. G. (2023) · Cancer treatment and research · doi:10.1007/978-3-031-45654-1_9 · Cited by 2
Unraveling the Roles of Canonical and Noncanonical PRC1 Complexes
Conway, E., & Bracken, A. P. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809737-3.00004-0 · Cited by 2
EZH2 as a therapeutic target in solid tumors
(2015) · Cancer Cell & Microenvironment · doi:10.14800/ccm.1024 · Cited by 2
Walter, J., & Hümpel, A. (2017) · Nomos Verlagsgesellschaft mbH & Co. KG eBooks · doi:10.5771/9783845270838 · Cited by 1
Neuroblastoma Epigenetic Landscape: Drugging Opportunities
Veschi, V., Durinck, K., Thiele, C. J., & Speleman, F. (2024) · Pediatric oncology · doi:10.1007/978-3-031-51292-6_5 · Cited by 2
Licciardello, M. P., & Kubicek, S. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802208-5.00009-6 · Cited by 2
Abali, G. K., Zhang, Y., Szeto, P., Zhao, P., Moghaddam, S. M., Leece, I., Huang, C., Cheung, J. G., Ameratunga, M., Noguchi, F., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.04.433988 · Cited by 2
Pavlović, S., & Tos̆ić, N. (2019) · Europeanization and globalization · doi:10.1007/978-3-030-16465-2_28 · Cited by 1
Radiosynthesis of [11C]EI1 for imaging EZH2 using positron emission tomography
Wang, H., Lan, Y., Bai, P., Chen, Z., Luo, S., Xu, Y., Fiedler, S. A., Striar, R., & Wang, C. (2020) · Medicinal Chemistry Research · doi:10.1007/s00044-020-02633-1 · Cited by 1
Identification of SET/EED Dual Binders As Innovative PRC2 Inhibitors
Catalano, R., Maruca, A., Rocca, R., Tassone, P., Panzarella, G., Costa, G., Ortuso, F., & Alcaro, S. (2022) · Future Medicinal Chemistry · doi:10.4155/fmc-2022-0010 · Cited by 1
Gorbunov, S., Kyriakou, S., Anestopoulos, I., Khoso, S., Manfredi, M., Franco, R., Pappa, A., & Panayiotidis, M. I. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27062647 · Cited by 1
Targeting EZH2 in Cancer: From Molecular Mechanisms to Clinical Translation
Zhong, X., Li, J., Pan, M., Ke, X., & Cui, H. (2026) · MedComm – Oncology · doi:10.1002/mog2.70070 · Cited by 1
Allosteric Inhibition of Polycomb Repressive Complex 2 by an EZH2‐Selective Small Molecule Inhibitor
Cao, T., Liu, D., Gao, H., Qin, C., Zhang, W., Lu, Z., Tan, D., Qu, Y.-X., Liu, Y., Zou, Z., et al. (2026) · Advanced Science · doi:10.1002/advs.76025 · Cited by 1
From design to clinic: Medicinal chemistry and pharmacology of approved epigenetic drugs
Penteado, A. B., Hassanie, H., Sousa, G. H. M., Vinha, T. C. N., Soares, A. C. G., Calil, R. L., dos Santos, T., Novais, R. M., Emery, F. D. S., Ganesan, A., et al. (2026) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2026.119198 · Cited by 1
Emerging Epigenetic Therapies—Lysine Methyltransferase/PRC Complex Inhibitors
Pande, V., Pocalyko, D. J., & Dhanak, D. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800206-3.00019-7 · Cited by 1
Inhibitors of Jumonji C-Domain Histone Demethylases
Staller, P. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800206-3.00020-3 · Cited by 1
Polycomb group genes as the key regulators in gene silencing
Su, S., Zhang, M., Li, L., & Wu, M. (2014) · Wuhan University Journal of Natural Sciences · doi:10.1007/s11859-014-0971-y · Cited by 1
504: Functional proteomic analysis of leukaemogenic protein tyrosine kinase targets
Azmi, N., Pierce, A., Williamson, A. J. K., & Whetton, A. D. (2014) · European Journal of Cancer · doi:10.1016/s0959-8049(14)50449-2 · Cited by 1
Trithorax and polycomb cooperation in MLL fusion acute leukemia
Méreau, H., & Schwaller, J. (2013) · Haematologica · doi:10.3324/haematol.2013.084301 · Cited by 1
DNA and Histone Modifications in Cancer Therapy
Suzuki, T. (2017) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-3-319-59786-7_20 · Cited by 1
Epigenetic therapies—update on lysine methyltransferase/PRC complex inhibitors
Kim, S., Barkey, N. M., Atasoylu, O., & Dhanak, D. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-91367-6.00011-8 · Cited by 1
Therapeutic Targeting of the Regulators of Cancer Epigenomes
Al-Janabi, I. I. (2023) · Al-Rafidain Journal of Medical Sciences · doi:10.54133/ajms.v5i.128 · Cited by 1
Recent Developments in the Structural Mechanism of Protein Methyltransferase Inhibition
Leung, R., & Schapira, M. (2024) · Royal Society of Chemistry eBooks · doi:10.1039/9781837674916-00084 · Cited by 1
Cacabelos, R., Naidoo, V., Tellado, I., Corzo, L., Cacabelos, N., Cacabelos, P., Martínez-Iglesias, O. A., & Segre, R. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-18722-3.00029-3 · Cited by 1
Therapeutic Applications of the Prostate Cancer Epigenome
Perry, A. S. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800206-3.00011-2 · Cited by 1
Histone Methylation Modifiers in Medical Therapeutics
Trojer, P. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803239-8.00037-5 · Cited by 1
Exploring the role of EZH2 (PRC2) as epigenetic target
Aier, I., & Raj, U. (2016) · International Conference on Bioinformatics and Systems Biology (BSB) · doi:10.1109/bsb.2016.7552131 · Cited by 1
Standard Chemotherapy Options and Clinical Trials of Novel Agents for Mesothelioma
Zauderer, M. G. (2017) · Current cancer research · doi:10.1007/978-3-319-53560-9_15 · Cited by 1
DNA and Histone Methylation in Prostate Cancer
Xu, K. (2017) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-3-319-59786-7_18 · Cited by 1
Control of Gene Expression by Nuclear Retinoic Acid Receptors
Carrier, M., & Rochette‐Egly, C. (2015) · doi:10.1002/9781118628003.ch5 · Cited by 1
Selective Small‐Molecule Inhibitors of Protein Methyltransferases
Kanıskan, H. Ü., & Jin, J. J. (2019) · Methods and principles in medicinal chemistry · doi:10.1002/9783527809257.ch9 · Cited by 1
Epigenetic Proteins as Emerging Drug Targets
Boriack‐Sjodin, P. A. (2020) · Wiley eBooks · doi:10.1002/9781118681121.ch18 · Cited by 1
A non-canonical EZH2 function sensitizes solid tumors to genotoxic stressPreprint
Liao, Y., Chen, C.-H., Shah, N., Xiao, T., Feit, A. S., Yang, M., Cai, C., Gao, S., Xue, P., Liu, Z., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.11.291534 · Cited by 1
The Function of the ASH1L Histone Methyltransferase in Cancer: A Chemical Biology Approach
Rogawski, D. S. (2016) · Deep Blue (University of Michigan) · Cited by 1
Heterochromatin fidelity is a therapeutic vulnerability in lymphoma and other human cancersPreprint
Najia, M. A. T., Jha, D. K., Zhang, C., Laurent, B., Kubaczka, C., Markel, A., Li, C., Morris, V., Tompkins, A., Hensch, L. T., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.31.635709 · Cited by 1
Animal Model Study of Epigenetic Inhibitors
Chen, A., & Huang, G. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801080-8.00020-x
Yakovenko, O., Leelakumari, S., Vashchenko, G., Cheung, P., Badiong, A., & Jones, S. J. M. (2015) · arXiv (Cornell University) · doi:10.48550/arxiv.1506.06433
Chemical Cryptology of Cancer’s Histone Code
Kulkarni, R. A., & Meier, J. L. (2014) · Chemistry & Biology · doi:10.1016/j.chembiol.2014.11.003
Familial and Somatic Mutations of Histone-Modifying Enzymes in Cancer
Liu, C., & Stein, L. D. (2013) · Springer eBooks · doi:10.1007/978-1-4614-7931-4_4
Asoke, K., & Casola, S. S. (2013)
Chromatin complex, crystal clear
Schapira, M. (2015) · Science · doi:10.1126/science.aad5203
Cheson, B. D., Zelenetz, A. D., Dreyling, M. H., Coiffier, B., Orsola‐Malpighi, S., & Ludwig Maximilians-University (2014)
Targeting Histone Lysine Methyltransferases in Cancer
Trojer, P. (2015) · Royal Society of Chemistry eBooks · doi:10.1039/9781782628484-00127
[The progress of diagnostic and prognostic molecular markers of lymphoma].
Zhang, M., Shi, Y., & Han, X. (2015) · PubMed Central · doi:10.3760/cma.j.issn.0253-2727.2015.04.022
The genetics of mature B‐cell malignancies
Strefford, J. C., Fitzgibbon, J., Rose-Zerilli, M. J. J., & Bödör, C. (2016) · Wiley eBooks · doi:10.1002/9781118527948.ch6
Metadata
- Authors
- Knutson, S. K., Wigle, T. J., Warholic, N. M., Sneeringer, C. J., Allain, C. J., Klaus, C. R., Sacks, J. D., Raimondi, A., Majer, C. R., Song, J., Scott, M. P., Jin, L., Smith, J. J., Olhava, E. J., Chesworth, R., Moyer, M. P., Richon, V. M., Copeland, R. A., Keilhack, H., Pollock, R. M., & Kuntz, K. W.
- Affiliations
- Epizyme (United States) (US)
- Corresponding author
- Kuntz, Kevin W
- ORCID
- Venue
- Nature Chemical Biology
- Published
- 2012-09-30
- Volume
- 8
- Issue
- 11
- Pages
- 890-896
- ISSN
- 1552-4450 (ISSN-L)
- 1552-4469
- OpenAlex
- W2017492512
- Cited by
- 776
- References
- 46
- Citations by year
- 2026: 20 · 2025: 29 · 2024: 29 · 2023: 39 · 2022: 38 · 2021: 49 · 2020: 42 · 2019: 44 · 2018: 60 · 2017: 83 · 2016: 78 · 2015: 97 · 2014: 89 · 2013: 69 · 2012: 10
- FWCI
- 34.74
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Chemical Biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cancer-related gene regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- EZH2, H3K27me3, polycomb repressive complex 2, EZH2 inhibitors, non-Hodgkin lymphoma, oncogene addiction, apoptosis, histone methyltransferase inhibitors
- MeSH terms
- Enhancer of Zeste Homolog 2 Protein, Antineoplastic Agents, Cell Cycle, Dose-Response Relationship, Drug, Enzyme Inhibitors, Histones, Humans, Indazoles, Lymphoma, Lysine, Methylation, Pyridones, Structure-Activity Relationship, Molecular Structure, Cell Death, Point Mutation, Cell Proliferation, Polycomb Repressive Complex 2
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