Roles of METTL3 in cancer: mechanisms and therapeutic targeting

被引:387
|
作者
Zeng, Chengwu [1 ,2 ]
Huang, Wanxu [1 ,3 ]
Li, Yangqiu [2 ]
Weng, Hengyou [1 ,4 ]
机构
[1] Guangzhou Regenerat Med & Hlth Guangdong Lab, Bioland Lab, Guangzhou 510005, Peoples R China
[2] Jinan Univ, Sch Med, Key Lab Regenerat Med, Inst Hematol,Minist Educ, Guangzhou 510632, Peoples R China
[3] Guangzhou Med Univ, Affiliated Hosp 5, Guangzhou 510700, Peoples R China
[4] Chinese Acad Sci, Guangzhou Inst Biomed & Hlth, Guangzhou 510530, Peoples R China
基金
中国国家自然科学基金;
关键词
RNA modification; METTL3; m(6)A; Cancer; Non-coding RNA; Drug discovery; MESSENGER-RNA METHYLATION; EPITHELIAL-MESENCHYMAL TRANSITION; M6A METHYLTRANSFERASE METTL3; M(6)A METHYLTRANSFERASE; COLORECTAL-CANCER; UP-REGULATION; NUCLEAR-RNA; N-6-METHYLADENOSINE MODIFICATION; HEPATOCELLULAR-CARCINOMA; TUMOR PROGRESSION;
D O I
10.1186/s13045-020-00951-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
N-6-methyladenosine (m(6)A) is the most abundant mRNA modification and is catalyzed by the methyltransferase complex, in which methyltransferase-like 3 (METTL3) is the sole catalytic subunit. Accumulating evidence in recent years reveals that METTL3 plays key roles in a variety of cancer types, either dependent or independent on its m(6)A RNA methyltransferase activity. While the roles of m(6)A modifications in cancer have been extensively reviewed elsewhere, the critical functions of METTL3 in various types of cancer, as well as the potential targeting of METTL3 as cancer treatment, have not yet been highlighted. Here we summarize our current understanding both on the oncogenic and tumor-suppressive functions of METTL3, as well as the underlying molecular mechanisms. The well-documented protein structure of the METTL3/METTL14 heterodimer provides the basis for potential therapeutic targeting, which is also discussed in this review.
引用
收藏
页数:15
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