» Articles » PMID: 35462896

The Emerging Role of N6-Methyladenosine RNA Methylation As Regulators in Cancer Therapy and Drug Resistance

Overview
Journal Front Pharmacol
Date 2022 Apr 25
PMID 35462896
Authors
Affiliations
Soon will be listed here.
Abstract

N6-methyladenosine (mA) RNA methylation has been considered the most prevalent, abundant, and conserved internal transcriptional modification throughout the eukaryotic mRNAs. Typically, mA RNA methylation is catalyzed by the RNA methyltransferases (writers), is removed by its demethylases (erasers), and interacts with mA-binding proteins (readers). Accumulating evidence shows that abnormal changes in the mA levels of these regulators are increasingly associated with human tumorigenesis and drug resistance. However, the molecular mechanisms underlying mA RNA methylation in tumor occurrence and development have not been comprehensively clarified. We reviewed the recent findings on biological regulation of mA RNA methylation and summarized its potential therapeutic strategies in various human cancers.

Citing Articles

Writers, readers, and erasers RNA modifications and drug resistance in cancer.

Chen D, Gu X, Nurzat Y, Xu L, Li X, Wu L Mol Cancer. 2024; 23(1):178.

PMID: 39215288 PMC: 11363509. DOI: 10.1186/s12943-024-02089-6.


PRMT6-mediated transcriptional activation of ythdf2 promotes glioblastoma migration, invasion, and emt via the wnt-β-catenin pathway.

Yu P, Xu T, Ma W, Fang X, Bao Y, Xu C J Exp Clin Cancer Res. 2024; 43(1):116.

PMID: 38637831 PMC: 11025288. DOI: 10.1186/s13046-024-03038-3.


Disruption of the mouse liver epitranscriptome by long-term aroclor 1260 exposure.

Piell K, Petri B, Head K, Wahlang B, Xu R, Zhang X Environ Toxicol Pharmacol. 2023; 100:104138.

PMID: 37137421 PMC: 10330322. DOI: 10.1016/j.etap.2023.104138.


Epigenetic Targets and Their Inhibitors in Thyroid Cancer Treatment.

Zhang K, Wang J, He Z, Qiu X, Sa R, Chen L Pharmaceuticals (Basel). 2023; 16(4).

PMID: 37111316 PMC: 10142462. DOI: 10.3390/ph16040559.


The Epitranscriptomic Mechanism of Metal Toxicity and Carcinogenesis.

Yang C, Wang Z Int J Mol Sci. 2022; 23(19).

PMID: 36233132 PMC: 9569618. DOI: 10.3390/ijms231911830.


References
1.
Dai X, Shi L, Li Z, Yang H, Wei J, Ding Q . Main N6-Methyladenosine Readers: YTH Family Proteins in Cancers. Front Oncol. 2021; 11:635329. PMC: 8076607. DOI: 10.3389/fonc.2021.635329. View

2.
Huang H, Wang Y, Kandpal M, Zhao G, Cardenas H, Ji Y . FTO-Dependent -Methyladenosine Modifications Inhibit Ovarian Cancer Stem Cell Self-Renewal by Blocking cAMP Signaling. Cancer Res. 2020; 80(16):3200-3214. PMC: 7442742. DOI: 10.1158/0008-5472.CAN-19-4044. View

3.
Rong D, Dong Q, Qu H, Deng X, Gao F, Li Q . mA-induced LINC00958 promotes breast cancer tumorigenesis via the miR-378a-3p/YY1 axis. Cell Death Discov. 2021; 7(1):27. PMC: 7854648. DOI: 10.1038/s41420-020-00382-z. View

4.
Hu J, Cai D, Zhao Z, Zhong G, Gong J . Suppression of Heterogeneous Nuclear Ribonucleoprotein C Inhibit Hepatocellular Carcinoma Proliferation, Migration, and Invasion Ras/MAPK Signaling Pathway. Front Oncol. 2021; 11:659676. PMC: 8087488. DOI: 10.3389/fonc.2021.659676. View

5.
Tanabe A, Tanikawa K, Tsunetomi M, Takai K, Ikeda H, Konno J . RNA helicase YTHDC2 promotes cancer metastasis via the enhancement of the efficiency by which HIF-1α mRNA is translated. Cancer Lett. 2016; 376(1):34-42. DOI: 10.1016/j.canlet.2016.02.022. View