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Cited by 926

The DOI matches its Crossref record; 97 of the 97 references it cites were found in a registry or an index.

EZH2: a novel target for cancer treatment

Open access
Duan, Ran, Du, Wenfang, Guo, Weijian·2020·Journal of Hematology & Oncology

Abstract

Enhancer of zeste homolog 2 (EZH2) is enzymatic catalytic subunit of polycomb repressive complex 2 (PRC2) that can alter downstream target genes expression by trimethylation of Lys-27 in histone 3 (H3K27me3). EZH2 could also regulate gene expression in ways besides H3K27me3. Functions of EZH2 in cells proliferation, apoptosis, and senescence have been identified. Its important roles in the pathophysiology of cancer are now widely concerned. Therefore, targeting EZH2 for cancer therapy is a hot research topic now and different types of EZH2 inhibitors have been developed. In this review, we summarize the structure and action modes of EZH2, focusing on up-to-date findings regarding the role of EZH2 in cancer initiation, progression, metastasis, metabolism, drug resistance, and immunity regulation. Furtherly, we highlight the advance of targeting EZH2 therapies in experiments and clinical studies.

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Crossref · 10.1186/s13045-020-00937-8

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Metadata

Authors
Duan, R., Du, W., & Guo, W.
Venue
Journal of Hematology & Oncology
Published
2020-07-28
Volume
13
Issue
1
Pages
104-104
ISSN
1756-8722 (ISSN-L)
OpenAlex
W3045753156
Cited by
926
References
97
FWCI
32.09
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: EZH2: a novel target for cancer treatment. https://app.cochat.ai/papers/10.1186/s13045-020-00937-8
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Duan, R., Du, W., & Guo, W. (2020). EZH2: a novel target for cancer treatment. Journal of Hematology & Oncology. https://doi.org/10.1186/s13045-020-00937-8

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.