Interaction between N6-methyladenosine modification and the tumor microenvironment in colorectal cancer

被引:2
|
作者
Yao, Jiali [1 ]
Song, Yeke [1 ]
Yu, Xiaoping [2 ]
Lin, Zhijie [1 ,3 ]
机构
[1] Yangzhou Univ, Dept Immunol, Inst Translat Med, Med Coll, Yangzhou 225009, Jiangsu, Peoples R China
[2] Yangzhou Univ, Affiliated Hosp, Hlth Management Ctr, Yangzhou 225009, Jiangsu, Peoples R China
[3] Yangzhou Univ, Jiangsu Key Lab Expt & Translat Noncoding RNA Res, Yangzhou 225001, Peoples R China
关键词
Colorectal cancer; m(6)A; Tumor microenvironment; NUCLEAR-RNA; INTESTINAL INFLAMMATION; DEMETHYLASE; N6-METHYLADENOSINE; INDUCTION; METTL14; CELLS;
D O I
10.1186/s10020-023-00726-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The incidence and mortality of colorectal cancer (CRC) are rapidly increasing worldwide. Recently, there has been significant attention given to N-6-methyladenosine (m(6)A), the most common mRNA modification, especially for its effects on CRC development. It is important to note that the progression of CRC would be greatly hindered without the tumor microenvironment (TME). The interaction between CRC cells and their surroundings can activate and influence complex signaling mechanisms of epigenetic changes to affect the survival of tumor cells with a malignant phenotype. Additionally, the TME is influenced by m(6)A regulatory factors, impacting the progression and prognosis of CRC. In this review, we describe the interactions and specific mechanisms between m(6)A modification and the metabolic, hypoxia, inflammatory, and immune microenvironments of CRC. Furthermore, we summarize the therapeutic role that m(6)A modification can play in the CRC microenvironment, and discuss the current status, limitations, and potential future directions in this field. This review aims to provide new insights into the molecular targets and theoretical foundations for the treatment of CRC.
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页数:15
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