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Epigenetic regulation in the tumor microenvironment: molecular mechanisms and therapeutic targets

Over decades, researchers have focused on the epigenetic control of DNA-templated processes. Histone modification, DNA methylation, chromatin remodeling, RNA modification, and noncoding RNAs modulate many biological processes that are crucial to the development of cancers. Dysregulation of the epige...

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Autores principales: Yang, Jing, Xu, Jin, Wang, Wei, Zhang, Bo, Yu, Xianjun, Shi, Si
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203321/
https://www.ncbi.nlm.nih.gov/pubmed/37217462
http://dx.doi.org/10.1038/s41392-023-01480-x
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author Yang, Jing
Xu, Jin
Wang, Wei
Zhang, Bo
Yu, Xianjun
Shi, Si
author_facet Yang, Jing
Xu, Jin
Wang, Wei
Zhang, Bo
Yu, Xianjun
Shi, Si
author_sort Yang, Jing
collection PubMed
description Over decades, researchers have focused on the epigenetic control of DNA-templated processes. Histone modification, DNA methylation, chromatin remodeling, RNA modification, and noncoding RNAs modulate many biological processes that are crucial to the development of cancers. Dysregulation of the epigenome drives aberrant transcriptional programs. A growing body of evidence suggests that the mechanisms of epigenetic modification are dysregulated in human cancers and might be excellent targets for tumor treatment. Epigenetics has also been shown to influence tumor immunogenicity and immune cells involved in antitumor responses. Thus, the development and application of epigenetic therapy and cancer immunotherapy and their combinations may have important implications for cancer treatment. Here, we present an up-to-date and thorough description of how epigenetic modifications in tumor cells influence immune cell responses in the tumor microenvironment (TME) and how epigenetics influence immune cells internally to modify the TME. Additionally, we highlight the therapeutic potential of targeting epigenetic regulators for cancer immunotherapy. Harnessing the complex interplay between epigenetics and cancer immunology to develop therapeutics that combine thereof is challenging but could yield significant benefits. The purpose of this review is to assist researchers in understanding how epigenetics impact immune responses in the TME, so that better cancer immunotherapies can be developed.
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spelling pubmed-102033212023-05-24 Epigenetic regulation in the tumor microenvironment: molecular mechanisms and therapeutic targets Yang, Jing Xu, Jin Wang, Wei Zhang, Bo Yu, Xianjun Shi, Si Signal Transduct Target Ther Review Article Over decades, researchers have focused on the epigenetic control of DNA-templated processes. Histone modification, DNA methylation, chromatin remodeling, RNA modification, and noncoding RNAs modulate many biological processes that are crucial to the development of cancers. Dysregulation of the epigenome drives aberrant transcriptional programs. A growing body of evidence suggests that the mechanisms of epigenetic modification are dysregulated in human cancers and might be excellent targets for tumor treatment. Epigenetics has also been shown to influence tumor immunogenicity and immune cells involved in antitumor responses. Thus, the development and application of epigenetic therapy and cancer immunotherapy and their combinations may have important implications for cancer treatment. Here, we present an up-to-date and thorough description of how epigenetic modifications in tumor cells influence immune cell responses in the tumor microenvironment (TME) and how epigenetics influence immune cells internally to modify the TME. Additionally, we highlight the therapeutic potential of targeting epigenetic regulators for cancer immunotherapy. Harnessing the complex interplay between epigenetics and cancer immunology to develop therapeutics that combine thereof is challenging but could yield significant benefits. The purpose of this review is to assist researchers in understanding how epigenetics impact immune responses in the TME, so that better cancer immunotherapies can be developed. Nature Publishing Group UK 2023-05-22 /pmc/articles/PMC10203321/ /pubmed/37217462 http://dx.doi.org/10.1038/s41392-023-01480-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Yang, Jing
Xu, Jin
Wang, Wei
Zhang, Bo
Yu, Xianjun
Shi, Si
Epigenetic regulation in the tumor microenvironment: molecular mechanisms and therapeutic targets
title Epigenetic regulation in the tumor microenvironment: molecular mechanisms and therapeutic targets
title_full Epigenetic regulation in the tumor microenvironment: molecular mechanisms and therapeutic targets
title_fullStr Epigenetic regulation in the tumor microenvironment: molecular mechanisms and therapeutic targets
title_full_unstemmed Epigenetic regulation in the tumor microenvironment: molecular mechanisms and therapeutic targets
title_short Epigenetic regulation in the tumor microenvironment: molecular mechanisms and therapeutic targets
title_sort epigenetic regulation in the tumor microenvironment: molecular mechanisms and therapeutic targets
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203321/
https://www.ncbi.nlm.nih.gov/pubmed/37217462
http://dx.doi.org/10.1038/s41392-023-01480-x
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