Epigenetic Regulation of NK Cell-Mediated Antitumor Immunity

被引:22
|
作者
Xia, Miaoran [1 ,2 ,3 ,4 ]
Wang, Bingbing [1 ,2 ,3 ,4 ]
Wang, Zihan [1 ,2 ,3 ,4 ]
Zhang, Xulong [1 ]
Wang, Xi [1 ,2 ,3 ,4 ]
机构
[1] Capital Med Univ, Sch Basic Med Sci, Dept Immunol, Beijing, Peoples R China
[2] Capital Med Univ, Adv Innovat Ctr Human Brain Protect, Beijing, Peoples R China
[3] Capital Med Univ, Beijing Key Lab Canc Invas & Metastasis Res, Beijing, Peoples R China
[4] Capital Med Univ, Dept Oncol, Beijing, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2021年 / 12卷
基金
中国国家自然科学基金;
关键词
natural killer (NK) cells; epigenetics; DNA methylation; histone modification; transcription factor; microRNA; antitumor immunity; NATURAL-KILLER-CELLS; CYTOTOXICITY; EXPRESSION; SUPPRESSION; ACTIVATION; MATURATION; RESPONSES;
D O I
10.3389/fimmu.2021.672328
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Natural killer (NK) cells are critical innate lymphocytes that can directly kill target cells without prior immunization. NK cell activation is controlled by the balance of multiple germline-encoded activating and inhibitory receptors. NK cells are a heterogeneous and plastic population displaying a broad spectrum of functional states (resting, activating, memory, repressed, and exhausted). In this review, we present an overview of the epigenetic regulation of NK cell-mediated antitumor immunity, including DNA methylation, histone modification, transcription factor changes, and microRNA expression. NK cell-based immunotherapy has been recognized as a promising strategy to treat cancer. Since epigenetic alterations are reversible and druggable, these studies will help identify new ways to enhance NK cell-mediated antitumor cytotoxicity by targeting intrinsic epigenetic regulators alone or in combination with other strategies.
引用
收藏
页数:13
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