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m6A modification: recent advances, anticancer targeted drug discovery and beyond
Abnormal N6-methyladenosine (m6A) modification is closely associated with the occurrence, development, progression and prognosis of cancer, and aberrant m6A regulators have been identified as novel anticancer drug targets. Both traditional medicine-related approaches and modern drug discovery platfo...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842557/ https://www.ncbi.nlm.nih.gov/pubmed/35164788 http://dx.doi.org/10.1186/s12943-022-01510-2 |
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author | Deng, Li-Juan Deng, Wei-Qing Fan, Shu-Ran Chen, Min-Feng Qi, Ming Lyu, Wen-Yu Qi, Qi Tiwari, Amit K. Chen, Jia-Xu Zhang, Dong-Mei Chen, Zhe-Sheng |
author_facet | Deng, Li-Juan Deng, Wei-Qing Fan, Shu-Ran Chen, Min-Feng Qi, Ming Lyu, Wen-Yu Qi, Qi Tiwari, Amit K. Chen, Jia-Xu Zhang, Dong-Mei Chen, Zhe-Sheng |
author_sort | Deng, Li-Juan |
collection | PubMed |
description | Abnormal N6-methyladenosine (m6A) modification is closely associated with the occurrence, development, progression and prognosis of cancer, and aberrant m6A regulators have been identified as novel anticancer drug targets. Both traditional medicine-related approaches and modern drug discovery platforms have been used in an attempt to develop m6A-targeted drugs. Here, we provide an update of the latest findings on m6A modification and the critical roles of m6A modification in cancer progression, and we summarize rational sources for the discovery of m6A-targeted anticancer agents from traditional medicines and computer-based chemosynthetic compounds. This review highlights the potential agents targeting m6A modification for cancer treatment and proposes the advantage of artificial intelligence (AI) in the discovery of m6A-targeting anticancer drugs. GRAPHICAL ABSTRACT: Three stages of m6A-targeting anticancer drug discovery: traditional medicine-based natural products, modern chemical modification or synthesis, and artificial intelligence (AI)-assisted approaches for the future. [Image: see text] |
format | Online Article Text |
id | pubmed-8842557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88425572022-02-16 m6A modification: recent advances, anticancer targeted drug discovery and beyond Deng, Li-Juan Deng, Wei-Qing Fan, Shu-Ran Chen, Min-Feng Qi, Ming Lyu, Wen-Yu Qi, Qi Tiwari, Amit K. Chen, Jia-Xu Zhang, Dong-Mei Chen, Zhe-Sheng Mol Cancer Review Abnormal N6-methyladenosine (m6A) modification is closely associated with the occurrence, development, progression and prognosis of cancer, and aberrant m6A regulators have been identified as novel anticancer drug targets. Both traditional medicine-related approaches and modern drug discovery platforms have been used in an attempt to develop m6A-targeted drugs. Here, we provide an update of the latest findings on m6A modification and the critical roles of m6A modification in cancer progression, and we summarize rational sources for the discovery of m6A-targeted anticancer agents from traditional medicines and computer-based chemosynthetic compounds. This review highlights the potential agents targeting m6A modification for cancer treatment and proposes the advantage of artificial intelligence (AI) in the discovery of m6A-targeting anticancer drugs. GRAPHICAL ABSTRACT: Three stages of m6A-targeting anticancer drug discovery: traditional medicine-based natural products, modern chemical modification or synthesis, and artificial intelligence (AI)-assisted approaches for the future. [Image: see text] BioMed Central 2022-02-14 /pmc/articles/PMC8842557/ /pubmed/35164788 http://dx.doi.org/10.1186/s12943-022-01510-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Deng, Li-Juan Deng, Wei-Qing Fan, Shu-Ran Chen, Min-Feng Qi, Ming Lyu, Wen-Yu Qi, Qi Tiwari, Amit K. Chen, Jia-Xu Zhang, Dong-Mei Chen, Zhe-Sheng m6A modification: recent advances, anticancer targeted drug discovery and beyond |
title | m6A modification: recent advances, anticancer targeted drug discovery and beyond |
title_full | m6A modification: recent advances, anticancer targeted drug discovery and beyond |
title_fullStr | m6A modification: recent advances, anticancer targeted drug discovery and beyond |
title_full_unstemmed | m6A modification: recent advances, anticancer targeted drug discovery and beyond |
title_short | m6A modification: recent advances, anticancer targeted drug discovery and beyond |
title_sort | m6a modification: recent advances, anticancer targeted drug discovery and beyond |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842557/ https://www.ncbi.nlm.nih.gov/pubmed/35164788 http://dx.doi.org/10.1186/s12943-022-01510-2 |
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