Methyltransferase-like proteins in cancer biology and potential therapeutic targeting

被引:46
|
作者
Qi, Ya-Nan [1 ]
Liu, Zhu [2 ,3 ]
Hong, Lian-Lian [2 ,3 ]
Li, Pei [1 ]
Ling, Zhi-Qiang [2 ,3 ]
机构
[1] Zhengzhou Univ, Sch Basic Med Sci, Dept Pathophysiol, Zhengzhou 450052, Peoples R China
[2] Zhejiang Canc Hosp, Zhejiang Canc Inst, 1 Banshan East Rd, Hangzhou 310022, Zhejiang, Peoples R China
[3] Chinese Acad Sci, Hangzhou Inst Med HIM, Hangzhou 310018, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
METTLs; Methyltransferase; Cancer biology; Therapeutics; Molecular mechanism; ELECTRON-TRANSFER FLAVOPROTEIN; RNA METHYLATION REGULATORS; CELL LUNG-CANCER; NF-KAPPA-B; M(6)A METHYLTRANSFERASE; MITOCHONDRIAL METHYLTRANSFERASE; LYSINE METHYLTRANSFERASE; MALIGNANT PROGRESSION; M6A MODIFICATION; BLADDER-CANCER;
D O I
10.1186/s13045-023-01477-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
RNA modification has recently become a significant process of gene regulation, and the methyltransferase-like (METTL) family of proteins plays a critical role in RNA modification, methylating various types of RNAs, including mRNA, tRNA, microRNA, rRNA, and mitochondrial RNAs. METTL proteins consist of a unique seven-beta-strand domain, which binds to the methyl donor SAM to catalyze methyl transfer. The most typical family member METTL3/METTL14 forms a methyltransferase complex involved in N6-methyladenosine (m6A) modification of RNA, regulating tumor proliferation, metastasis and invasion, immunotherapy resistance, and metabolic reprogramming of tumor cells. METTL1, METTL4, METTL5, and METTL16 have also been recently identified to have some regulatory ability in tumorigenesis, and the rest of the METTL family members rely on their methyltransferase activity for methylation of different nucleotides, proteins, and small molecules, which regulate translation and affect processes such as cell differentiation and development. Herein, we summarize the literature on METTLs in the last three years to elucidate their roles in human cancers and provide a theoretical basis for their future use as potential therapeutic targets.
引用
收藏
页数:35
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