» Articles » PMID: 33461542

The Role of MA, MC and Ψ RNA Modifications in Cancer: Novel Therapeutic Opportunities

Overview
Journal Mol Cancer
Publisher Biomed Central
Date 2021 Jan 19
PMID 33461542
Citations 237
Authors
Affiliations
Soon will be listed here.
Abstract

RNA modifications have recently emerged as critical posttranscriptional regulators of gene expression programmes. Significant advances have been made in understanding the functional role of RNA modifications in regulating coding and non-coding RNA processing and function, which in turn thoroughly shape distinct gene expression programmes. They affect diverse biological processes, and the correct deposition of many of these modifications is required for normal development. Alterations of their deposition are implicated in several diseases, including cancer. In this Review, we focus on the occurrence of N-methyladenosine (mA), 5-methylcytosine (mC) and pseudouridine (Ψ) in coding and non-coding RNAs and describe their physiopathological role in cancer. We will highlight the latest insights into the mechanisms of how these posttranscriptional modifications influence tumour development, maintenance, and progression. Finally, we will summarize the latest advances on the development of small molecule inhibitors that target specific writers or erasers to rewind the epitranscriptome of a cancer cell and their therapeutic potential.

Citing Articles

Biological functions of 5-methylcytosine RNA-binding proteins and their potential mechanisms in human cancers.

Zhao T, Zhang Z, Chen Z, Xu G, Wang Y, Wang F Front Oncol. 2025; 15:1534948.

PMID: 39990690 PMC: 11842269. DOI: 10.3389/fonc.2025.1534948.


The Mechanisms, Research Status, and Future Prospects of m6A Modification in Breast Cancer.

Xue-Mei X, Yang C, Wen-Ting J, Wen-Xing Q J Gene Med. 2025; 27(2):e70014.

PMID: 39972939 PMC: 11840220. DOI: 10.1002/jgm.70014.


RBM15 recruits myeloid-derived suppressor cells via the m6A-IGF2BP3/CBR3-AS1/miR-409-3p/CXCL1 axis, facilitating radioresistance in non-small-cell lung cancer.

Hu S, Zhan N, Li J, Wang L, Liu Y, Jin K J Transl Med. 2025; 23(1):191.

PMID: 39962467 PMC: 11831794. DOI: 10.1186/s12967-025-06205-y.


NSUN7 promotes cervical cancer progression through activation of ErbB signaling pathway.

Li Y, Lu R, Abuduhailili X, Feng Y Funct Integr Genomics. 2025; 25(1):37.

PMID: 39954044 DOI: 10.1007/s10142-025-01546-9.


mRNA Transcript Variants Expressed in Mammalian Cells.

Sharma Y, Vo K, Shila S, Paul A, Dahiya V, Fields P Int J Mol Sci. 2025; 26(3).

PMID: 39940824 PMC: 11817330. DOI: 10.3390/ijms26031052.


References
1.
Knuckles P, Lence T, Haussmann I, Jacob D, Kreim N, Carl S . Zc3h13/Flacc is required for adenosine methylation by bridging the mRNA-binding factor Rbm15/Spenito to the mA machinery component Wtap/Fl(2)d. Genes Dev. 2018; 32(5-6):415-429. PMC: 5900714. DOI: 10.1101/gad.309146.117. View

2.
Hamma T, Ferre-DAmare A . Pseudouridine synthases. Chem Biol. 2006; 13(11):1125-35. DOI: 10.1016/j.chembiol.2006.09.009. View

3.
Eyler D, Franco M, Batool Z, Wu M, Dubuke M, Dobosz-Bartoszek M . Pseudouridinylation of mRNA coding sequences alters translation. Proc Natl Acad Sci U S A. 2019; 116(46):23068-23074. PMC: 6859337. DOI: 10.1073/pnas.1821754116. View

4.
Freeman J, McGrath P, Bondada V, Selliah N, Ownby H, Maloney T . Prognostic significance of proliferation associated nucleolar antigen P120 in human breast carcinoma. Cancer Res. 1991; 51(8):1973-8. View

5.
Ueda Y, Ooshio I, Fusamae Y, Kitae K, Kawaguchi M, Jingushi K . AlkB homolog 3-mediated tRNA demethylation promotes protein synthesis in cancer cells. Sci Rep. 2017; 7:42271. PMC: 5304225. DOI: 10.1038/srep42271. View