Dysregulation of DNA methylation in colorectal cancer: biomarker, immune regulation, and therapeutic potential

被引:1
作者
Wang, Qin [1 ,2 ]
Ma, Chen [1 ]
Yang, Bin [3 ]
Zheng, Wenxin [1 ]
Liu, Xinya [1 ]
Jian, Gu [1 ]
机构
[1] Southwest Minzu Univ, Sch Pharm, Chengdu, Peoples R China
[2] Natl Univ Singapore, Yong Yoo Lin Sch Med, Dept Pathol, Singapore, Singapore
[3] Capital Med Univ, Sch Tradit Chinese Med, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA methylation; Colorectal cancer; Clinical practice; Diagnosis; Tumor immune microenvironment; HISTONE DEMETHYLASES; COLON-CANCER; PROMOTER; BINDING; PROTEIN; TRANSCRIPTION; CELLS; 5-METHYLCYTOSINE; HYPERMETHYLATION; MECHANISMS;
D O I
10.1016/j.intimp.2024.113766
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Colorectal cancer (CRC) is one of the most prevalent malignancies worldwide, with morbidity and mortality ranking third and second among all cancers, respectively. As a result of a sequence of genetic and DNA methylation alterations that gradually accumulate in the healthy colonic epithelium, colorectal adenomas and invasive adenocarcinomas eventually give rise to CRC. Global hypomethylation and promoter-specific DNA methylation are characteristics of CRC. The pathophysiological role of aberrant DNA methylation in malignant tumors has garnered significant interest in the last few decades. In addition, DNA methylation has been shown to play a critical role in influencing immune cell function and tumor immune evasion. This review summarizes the most recent research on DNA methylation changes in CRC, including the role of DNA methylation-related enzymes in CRC tumorigenesis and biomarkers for diagnosis, predictive and prognostic. Besides, we focus on the emerging potential of epigenetic interventions to enhance antitumor immune responses and improve the CRC clinical practice.
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页数:9
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