免疫系统
核糖核酸
癌变
表观遗传学
生物
肿瘤微环境
癌症研究
癌细胞
RNA甲基化
癌症
甲基化
免疫学
基因
甲基转移酶
遗传学
作者
Xinyu Gu,Xiao Ma,Chao Chen,Jun Guan,Jing Wang,Shanshan Wu,Haihong Zhu
标识
DOI:10.3389/fimmu.2023.1207371
摘要
RNA modification plays an important role in epigenetics at the posttranscriptional level, and 5-methylcytosine (m 5 C) has attracted increasing attention in recent years due to the improvement in RNA m 5 C site detection methods. By influencing transcription, transportation and translation, m 5 C modification of mRNA, tRNA, rRNA, lncRNA and other RNAs has been proven to affect gene expression and metabolism and is associated with a wide range of diseases, including malignant cancers. RNA m 5 C modifications also substantially impact the tumor microenvironment (TME) by targeting different groups of immune cells, including B cells, T cells, macrophages, granulocytes, NK cells, dendritic cells and mast cells. Alterations in immune cell expression, infiltration and activation are highly linked to tumor malignancy and patient prognosis. This review provides a novel and holistic examination of m 5 C-mediated cancer development by examining the exact mechanisms underlying the oncogenicity of m 5 C RNA modification and summarizing the biological effects of m 5 C RNA modification on tumor cells as well as immune cells. Understanding methylation-related tumorigenesis can provide useful insights for the diagnosis as well as the treatment of cancer.
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