» Articles » PMID: 39459530

Clinician's Guide to Epitranscriptomics: An Example of N-Methyladenosine (mA) RNA Modification and Cancer

Overview
Journal Life (Basel)
Specialty Biology
Date 2024 Oct 26
PMID 39459530
Authors
Affiliations
Soon will be listed here.
Abstract

Epitranscriptomics is the study of modifications of RNA molecules by small molecular residues, such as the methyl (-CH) group. These modifications are inheritable and reversible. A specific group of enzymes called "writers" introduces the change to the RNA; "erasers" delete it, while "readers" stimulate a downstream effect. Epitranscriptomic changes are present in every type of organism from single-celled ones to plants and animals and are a key to normal development as well as pathologic processes. Oncology is a fast-paced field, where a better understanding of tumor biology and (epi)genetics is necessary to provide new therapeutic targets and better clinical outcomes. Recently, changes to the epitranscriptome have been shown to be drivers of tumorigenesis, biomarkers, and means of predicting outcomes, as well as potential therapeutic targets. In this review, we aimed to give a concise overview of epitranscriptomics in the context of neoplastic disease with a focus on N-methyladenosine (mA) modification, in layman's terms, to bring closer this omics to clinicians and their future clinical practice.

References
1.
Fang Z, Hu Y, Hong X, Zhang X, Pan T, Pan C . Simultaneous Determination of Methylated Nucleosides by HILIC-MS/MS Revealed Their Alterations in Urine from Breast Cancer Patients. Metabolites. 2022; 12(10). PMC: 9612034. DOI: 10.3390/metabo12100973. View

2.
Oerum S, Catala M, Atdjian C, Brachet F, Ponchon L, Barraud P . Bisubstrate analogues as structural tools to investigate mA methyltransferase active sites. RNA Biol. 2019; 16(6):798-808. PMC: 6546350. DOI: 10.1080/15476286.2019.1589360. View

3.
Zhou H, Kimsey I, Nikolova E, Sathyamoorthy B, Grazioli G, McSally J . m(1)A and m(1)G disrupt A-RNA structure through the intrinsic instability of Hoogsteen base pairs. Nat Struct Mol Biol. 2016; 23(9):803-10. PMC: 5016226. DOI: 10.1038/nsmb.3270. View

4.
Marikovsky M . Thiram inhibits angiogenesis and slows the development of experimental tumours in mice. Br J Cancer. 2002; 86(5):779-87. PMC: 2375322. DOI: 10.1038/sj.bjc.6600078. View

5.
Li J, Zhang H, Wang H . N-methyladenosine modification in cancer biology: Current status and future perspectives. Comput Struct Biotechnol J. 2022; 20:6578-6585. PMC: 9712505. DOI: 10.1016/j.csbj.2022.11.045. View