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The role of regulators of RNA m(6)A methylation in lung cancer

N(6)-methyladenosine (m(6)A) modification is found the most prevalent and abundant post-transcriptional mRNA modification in eukaryotic cells. It regulates almost all stages of RNA life cycle including splicing, translocation, stability, decay and translation. As a dynamic and reversible process, m(...

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Autores principales: Zhang, Qicheng, Xu, Ke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201596/
https://www.ncbi.nlm.nih.gov/pubmed/37223516
http://dx.doi.org/10.1016/j.gendis.2021.12.017
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author Zhang, Qicheng
Xu, Ke
author_facet Zhang, Qicheng
Xu, Ke
author_sort Zhang, Qicheng
collection PubMed
description N(6)-methyladenosine (m(6)A) modification is found the most prevalent and abundant post-transcriptional mRNA modification in eukaryotic cells. It regulates almost all stages of RNA life cycle including splicing, translocation, stability, decay and translation. As a dynamic and reversible process, m(6)A modification is catalyzed by the RNA methyltransferases (‘writers’), removed by the demethylases (‘erasers’), and interacts with m(6)A-binding proteins (‘readers’). Recent studies have revealed that these m(6)A modification regulators are frequently expressed aberrantly in various types of cancer, and involved in cell proliferation, differentiation, metabolism, particularly, in tumorigenesis and tumor progression through diverse mechanisms. In this review, the m(6)A modification process and its regulatory functions in lung cancer are summarized. Furthermore, the research progress in the inhibitor development of m(6)A modification, and the potential of targeting m(6)A modifying proteins for clinical application are discussed.
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spelling pubmed-102015962023-05-23 The role of regulators of RNA m(6)A methylation in lung cancer Zhang, Qicheng Xu, Ke Genes Dis Review Article N(6)-methyladenosine (m(6)A) modification is found the most prevalent and abundant post-transcriptional mRNA modification in eukaryotic cells. It regulates almost all stages of RNA life cycle including splicing, translocation, stability, decay and translation. As a dynamic and reversible process, m(6)A modification is catalyzed by the RNA methyltransferases (‘writers’), removed by the demethylases (‘erasers’), and interacts with m(6)A-binding proteins (‘readers’). Recent studies have revealed that these m(6)A modification regulators are frequently expressed aberrantly in various types of cancer, and involved in cell proliferation, differentiation, metabolism, particularly, in tumorigenesis and tumor progression through diverse mechanisms. In this review, the m(6)A modification process and its regulatory functions in lung cancer are summarized. Furthermore, the research progress in the inhibitor development of m(6)A modification, and the potential of targeting m(6)A modifying proteins for clinical application are discussed. Chongqing Medical University 2022-01-29 /pmc/articles/PMC10201596/ /pubmed/37223516 http://dx.doi.org/10.1016/j.gendis.2021.12.017 Text en © 2022 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Zhang, Qicheng
Xu, Ke
The role of regulators of RNA m(6)A methylation in lung cancer
title The role of regulators of RNA m(6)A methylation in lung cancer
title_full The role of regulators of RNA m(6)A methylation in lung cancer
title_fullStr The role of regulators of RNA m(6)A methylation in lung cancer
title_full_unstemmed The role of regulators of RNA m(6)A methylation in lung cancer
title_short The role of regulators of RNA m(6)A methylation in lung cancer
title_sort role of regulators of rna m(6)a methylation in lung cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201596/
https://www.ncbi.nlm.nih.gov/pubmed/37223516
http://dx.doi.org/10.1016/j.gendis.2021.12.017
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