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Targeting Key RNA Methylation Enzymes to Improve the Outcome of Colorectal Cancer Chemotherapy (Review)

Overview
Journal Int J Oncol
Specialty Oncology
Date 2023 Dec 22
PMID 38131226
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Abstract

RNA methylation modifications are closely linked to tumor development, migration, invasion and responses to various therapies. Recent studies have shown notable advancements regarding the roles of RNA methylation in tumor immunotherapy, the tumor microenvironment and metabolic reprogramming. However, research on the association between tumor chemoresistance and N6‑methyladenosine (m6A) methyltransferases in specific cancer types is still scarce. Colorectal cancer (CRC) is among the most common gastrointestinal cancers worldwide. Conventional chemotherapy remains the predominant treatment modality for CRC and chemotherapy resistance is the primary cause of treatment failure. The expression levels of m6A methyltransferases, including methyltransferase‑like 3 (METTL3), METTL14 and METTL16, in CRC tissue samples are associated with patients' clinical outcomes and chemotherapy efficacy. Natural pharmaceutical ingredients, such as quercetin, have the potential to act as METTL3 inhibitors to combat chemotherapy resistance in patients with CRC. The present review discussed the various roles of different types of key RNA methylation enzymes in the development of CRC, focusing on the mechanisms associated with chemotherapy resistance. The progress in the development of certain inhibitors is also listed. The potential of using natural remedies to develop antitumor medications that target m6A methylation is also outlined.

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References
1.
Wang Y, Yang L, Zhang J, Zhou M, Shen L, Deng W . Radiosensitization by irinotecan is attributed to G2/M phase arrest, followed by enhanced apoptosis, probably through the ATM/Chk/Cdc25C/Cdc2 pathway in p53-mutant colorectal cancer cells. Int J Oncol. 2018; 53(4):1667-1680. DOI: 10.3892/ijo.2018.4514. View

2.
Lu S, Han L, Hu X, Sun T, Xu D, Li Y . N6-methyladenosine reader IMP2 stabilizes the ZFAS1/OLA1 axis and activates the Warburg effect: implication in colorectal cancer. J Hematol Oncol. 2021; 14(1):188. PMC: 8574039. DOI: 10.1186/s13045-021-01204-0. View

3.
Ma S, Zhang J, Yan T, Miao M, Cao Y, Cao Y . Novel strategies to reverse chemoresistance in colorectal cancer. Cancer Med. 2023; 12(10):11073-11096. PMC: 10242875. DOI: 10.1002/cam4.5594. View

4.
Lin Z, Wan A, Sun L, Liang H, Niu Y, Deng Y . N6-methyladenosine demethylase FTO enhances chemo-resistance in colorectal cancer through SIVA1-mediated apoptosis. Mol Ther. 2022; 31(2):517-534. PMC: 9931553. DOI: 10.1016/j.ymthe.2022.10.012. View

5.
Liu K, Ouyang Q, Zhan Y, Yin H, Liu B, Tan L . Pharmacoepitranscriptomic landscape revealing m6A modification could be a drug-effect biomarker for cancer treatment. Mol Ther Nucleic Acids. 2022; 28:464-476. PMC: 9044172. DOI: 10.1016/j.omtn.2022.04.001. View