Methyltransferase-like proteins in cancer biology and potential therapeutic targeting

被引:64
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
相关论文
共 295 条
[1]   Role of m6A RNA Methylation in Thyroid Cancer Cell Lines [J].
Allegri, Lorenzo ;
Baldan, Federica ;
Molteni, Elisabetta ;
Mio, Catia ;
Damante, Giuseppe .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (19)
[2]   Mechanistic insights into m6A modification of U6 snRNA by human METTL16 [J].
Aoyama, Tomohiko ;
Yamashita, Seisuke ;
Tomita, Kozo .
NUCLEIC ACIDS RESEARCH, 2020, 48 (09) :5157-5168
[3]   Molecular analysis of METTL1, a novel human methyltransferase-like gene with a high degree of phylogenetic conservation [J].
Bahr, A ;
Hankeln, T ;
Fiedler, T ;
Hegemann, J ;
Schmidt, ER .
GENOMICS, 1999, 57 (03) :424-428
[4]   The LIN28/let-7 Pathway in Cancer [J].
Balzeau, Julien ;
Menezes, Miriam R. ;
Cao, Siyu ;
Hagan, John P. .
FRONTIERS IN GENETICS, 2017, 8 :1-16
[5]   LNCAROD is stabilized by m6A methylation and promotes cancer progression via forming a ternary complex with HSPA1A and YBX1 in head and neck squamous cell carcinoma [J].
Ban, Yuanyuan ;
Tan, Pingqing ;
Cai, Jing ;
Li, Junjun ;
Hu, Meng ;
Zhou, Ying ;
Mei, Yan ;
Tan, Yixin ;
Li, Xiaoling ;
Zeng, Zhaoyang ;
Xiong, Wei ;
Li, Guiyuan ;
Li, Xiayu ;
Yi, Mei ;
Xiang, Bo .
MOLECULAR ONCOLOGY, 2020, 14 (06) :1282-1296
[6]   Small-Molecule Inhibitors of METTL3, the Major Human Epitranscriptomic Writer [J].
Bedi, Rajiv K. ;
Huang Danzhi ;
Eberle, Stefanie A. ;
Wiedmer, Lars ;
Sledz, Pawel ;
Caflisch, Amedeo .
CHEMMEDCHEM, 2020, 15 (09) :744-748
[7]   METTL3 induces PLX4032 resistance in melanoma by promoting m6A-dependent EGFR translation [J].
Bhattarai, Poshan Yugal ;
Kim, Garam ;
Poudel, Muna ;
Lim, Sung-Chul ;
Choi, Hong Seok .
CANCER LETTERS, 2021, 522 :44-56
[8]   METTL3 promotes the initiation and metastasis of ovarian cancer by inhibiting CCNG2 expression via promoting the maturation of pri-microRNA-1246 [J].
Bi, Xuehan ;
Lv, Xiao ;
Liu, Dajiang ;
Guo, Hongtao ;
Yao, Guang ;
Wang, Lijuan ;
Liang, Xiaolei ;
Yang, Yongxiu .
CELL DEATH DISCOVERY, 2021, 7 (01)
[9]   METTL3-mediated maturation of miR-126-5p promotes ovarian cancer progression via PTEN-mediated PI3K/Akt/mTOR pathway [J].
Bi, Xuehan ;
Lv, Xiao ;
Liu, Dajiang ;
Guo, Hongtao ;
Yao, Guang ;
Wang, Lijuan ;
Liang, Xiaolei ;
Yang, Yongxiu .
CANCER GENE THERAPY, 2021, 28 (3-4) :335-349
[10]  
Bokar JA, 1997, RNA, V3, P1233