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Cited by 346

The DOI matches its Crossref record; 90 of the 90 references it cites were found in a registry or an index.

Cancer Epigenetics, Tumor Immunity, and Immunotherapy

Open access
Cao, Jian, Yan, Qin·2020·Trends in Cancer

Abstract

Epigenetic mechanisms, including DNA methylation, histone post-translational modifications, and chromatin structure regulation, are critical for the interactions between tumor and immune cells. Emerging evidence shows that tumors commonly hijack various epigenetic mechanisms to escape immune restriction. As a result, the pharmaceutical modulation of epigenetic regulators, including ‘writers’, ‘readers’, ‘erasers’, and ‘remodelers’, is able to normalize the impaired immunosurveillance and/or trigger antitumor immune responses. Thus, epigenetic targeting agents are attractive immunomodulatory drugs and will have major impacts on immuno-oncology. Here, we discuss epigenetic regulators of the cancer–immunity cycle and current advances in developing epigenetic therapies to boost anticancer immune responses, either alone or in combination with current immunotherapies.

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Crossref · 10.1016/j.trecan.2020.02.003

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Metadata

Authors
Cao, J., & Yan, Q.
Venue
Trends in Cancer
Publisher
Elsevier BV
Published
2020-07
Volume
6
Issue
7
Pages
580-592
ISSN
  • 2405-8025 (ISSN-L)
  • 2405-8033
OpenAlex
W3015068997
Cited by
346
References
90
FWCI
3.50
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Cancer Epigenetics, Tumor Immunity, and Immunotherapy. https://app.cochat.ai/papers/10.1016/j.trecan.2020.02.003
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Cao, J., & Yan, Q. (2020). Cancer Epigenetics, Tumor Immunity, and Immunotherapy. Trends in Cancer. https://doi.org/10.1016/j.trecan.2020.02.003

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

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.