Targeting the RNA m6A modification for cancer immunotherapy

Abstract N 6-methyladenosine (m6A) is the most abundant epigenetic modification of RNA, and its dysregulation drives aberrant transcription and translation programs that promote cancer occurrence and progression. Although defective gene regulation resulting from m6A often affects oncogenic and tumor...

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Main Authors: Xinxin Li, Shoubao Ma, Youcai Deng, Ping Yi, Jianhua Yu
Format: Article
Language:English
Published: BMC 2022-03-01
Series:Molecular Cancer
Subjects:
Online Access:https://doi.org/10.1186/s12943-022-01558-0
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author Xinxin Li
Shoubao Ma
Youcai Deng
Ping Yi
Jianhua Yu
author_facet Xinxin Li
Shoubao Ma
Youcai Deng
Ping Yi
Jianhua Yu
author_sort Xinxin Li
collection DOAJ
description Abstract N 6-methyladenosine (m6A) is the most abundant epigenetic modification of RNA, and its dysregulation drives aberrant transcription and translation programs that promote cancer occurrence and progression. Although defective gene regulation resulting from m6A often affects oncogenic and tumor-suppressing networks, m6A can also modulate tumor immunogenicity and immune cells involved in anti-tumor responses. Understanding this counterintuitive concept can aid the design of new drugs that target m6A to potentially improve the outcomes of cancer immunotherapies. Here, we provide an up-to-date and comprehensive overview of how m6A modifications intrinsically affect immune cells and how alterations in tumor cell m6A modifications extrinsically affect immune cell responses in the tumor microenvironment (TME). We also review strategies for modulating endogenous anti-tumor immunity and discuss the challenge of reshaping the TME. Strategies include: combining specific and efficient inhibitors against m6A regulators with immune checkpoint blockers; generating an effective programmable m6A gene-editing system that enables efficient manipulation of individual m6A sites; establishing an effective m6A modification system to enhance anti-tumor immune responses in T cells or natural killer cells; and using nanoparticles that specifically target tumor-associated macrophages (TAMs) to deliver messenger RNA or small interfering RNA of m6A-related molecules that repolarize TAMs, enabling them to remodel the TME. The goal of this review is to help the field understand how m6A modifications intrinsically and extrinsically shape immune responses in the TME so that better cancer immunotherapy can be designed and developed.
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spelling doaj.art-b7281cbe5ff24099bba641c1f4c5ce252022-12-21T23:51:28ZengBMCMolecular Cancer1476-45982022-03-0121111610.1186/s12943-022-01558-0Targeting the RNA m6A modification for cancer immunotherapyXinxin Li0Shoubao Ma1Youcai Deng2Ping Yi3Jianhua Yu4Xi’an Key Laboratory of Stem Cell and Regenerative Medicine, Institute of Medical Research, Northwestern Polytechnical UniversityDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical CenterInstitute of Materia Medica, College of Pharmacy, Army Medical UniversityDepartment of Obstetrics and Gynecology, The Third Affiliated Hospital of Chongqing Medical UniversityDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical CenterAbstract N 6-methyladenosine (m6A) is the most abundant epigenetic modification of RNA, and its dysregulation drives aberrant transcription and translation programs that promote cancer occurrence and progression. Although defective gene regulation resulting from m6A often affects oncogenic and tumor-suppressing networks, m6A can also modulate tumor immunogenicity and immune cells involved in anti-tumor responses. Understanding this counterintuitive concept can aid the design of new drugs that target m6A to potentially improve the outcomes of cancer immunotherapies. Here, we provide an up-to-date and comprehensive overview of how m6A modifications intrinsically affect immune cells and how alterations in tumor cell m6A modifications extrinsically affect immune cell responses in the tumor microenvironment (TME). We also review strategies for modulating endogenous anti-tumor immunity and discuss the challenge of reshaping the TME. Strategies include: combining specific and efficient inhibitors against m6A regulators with immune checkpoint blockers; generating an effective programmable m6A gene-editing system that enables efficient manipulation of individual m6A sites; establishing an effective m6A modification system to enhance anti-tumor immune responses in T cells or natural killer cells; and using nanoparticles that specifically target tumor-associated macrophages (TAMs) to deliver messenger RNA or small interfering RNA of m6A-related molecules that repolarize TAMs, enabling them to remodel the TME. The goal of this review is to help the field understand how m6A modifications intrinsically and extrinsically shape immune responses in the TME so that better cancer immunotherapy can be designed and developed.https://doi.org/10.1186/s12943-022-01558-0Tumor microenvironmentCancer immunotherapyEpigeneticsN 6-methyladenosinem6A modificationm6A regulators
spellingShingle Xinxin Li
Shoubao Ma
Youcai Deng
Ping Yi
Jianhua Yu
Targeting the RNA m6A modification for cancer immunotherapy
Molecular Cancer
Tumor microenvironment
Cancer immunotherapy
Epigenetics
N 6-methyladenosine
m6A modification
m6A regulators
title Targeting the RNA m6A modification for cancer immunotherapy
title_full Targeting the RNA m6A modification for cancer immunotherapy
title_fullStr Targeting the RNA m6A modification for cancer immunotherapy
title_full_unstemmed Targeting the RNA m6A modification for cancer immunotherapy
title_short Targeting the RNA m6A modification for cancer immunotherapy
title_sort targeting the rna m6a modification for cancer immunotherapy
topic Tumor microenvironment
Cancer immunotherapy
Epigenetics
N 6-methyladenosine
m6A modification
m6A regulators
url https://doi.org/10.1186/s12943-022-01558-0
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