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Roles of METTL3 in cancer: mechanisms and therapeutic targeting
N(6)-methyladenosine (m(6)A) is the most abundant mRNA modification and is catalyzed by the methyltransferase complex, in which methyltransferase-like 3 (METTL3) is the sole catalytic subunit. Accumulating evidence in recent years reveals that METTL3 plays key roles in a variety of cancer types, eit...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457244/ https://www.ncbi.nlm.nih.gov/pubmed/32854717 http://dx.doi.org/10.1186/s13045-020-00951-w |
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author | Zeng, Chengwu Huang, Wanxu Li, Yangqiu Weng, Hengyou |
author_facet | Zeng, Chengwu Huang, Wanxu Li, Yangqiu Weng, Hengyou |
author_sort | Zeng, Chengwu |
collection | PubMed |
description | N(6)-methyladenosine (m(6)A) is the most abundant mRNA modification and is catalyzed by the methyltransferase complex, in which methyltransferase-like 3 (METTL3) is the sole catalytic subunit. Accumulating evidence in recent years reveals that METTL3 plays key roles in a variety of cancer types, either dependent or independent on its m(6)A RNA methyltransferase activity. While the roles of m(6)A modifications in cancer have been extensively reviewed elsewhere, the critical functions of METTL3 in various types of cancer, as well as the potential targeting of METTL3 as cancer treatment, have not yet been highlighted. Here we summarize our current understanding both on the oncogenic and tumor-suppressive functions of METTL3, as well as the underlying molecular mechanisms. The well-documented protein structure of the METTL3/METTL14 heterodimer provides the basis for potential therapeutic targeting, which is also discussed in this review. |
format | Online Article Text |
id | pubmed-7457244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74572442020-08-31 Roles of METTL3 in cancer: mechanisms and therapeutic targeting Zeng, Chengwu Huang, Wanxu Li, Yangqiu Weng, Hengyou J Hematol Oncol Review N(6)-methyladenosine (m(6)A) is the most abundant mRNA modification and is catalyzed by the methyltransferase complex, in which methyltransferase-like 3 (METTL3) is the sole catalytic subunit. Accumulating evidence in recent years reveals that METTL3 plays key roles in a variety of cancer types, either dependent or independent on its m(6)A RNA methyltransferase activity. While the roles of m(6)A modifications in cancer have been extensively reviewed elsewhere, the critical functions of METTL3 in various types of cancer, as well as the potential targeting of METTL3 as cancer treatment, have not yet been highlighted. Here we summarize our current understanding both on the oncogenic and tumor-suppressive functions of METTL3, as well as the underlying molecular mechanisms. The well-documented protein structure of the METTL3/METTL14 heterodimer provides the basis for potential therapeutic targeting, which is also discussed in this review. BioMed Central 2020-08-27 /pmc/articles/PMC7457244/ /pubmed/32854717 http://dx.doi.org/10.1186/s13045-020-00951-w Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Zeng, Chengwu Huang, Wanxu Li, Yangqiu Weng, Hengyou Roles of METTL3 in cancer: mechanisms and therapeutic targeting |
title | Roles of METTL3 in cancer: mechanisms and therapeutic targeting |
title_full | Roles of METTL3 in cancer: mechanisms and therapeutic targeting |
title_fullStr | Roles of METTL3 in cancer: mechanisms and therapeutic targeting |
title_full_unstemmed | Roles of METTL3 in cancer: mechanisms and therapeutic targeting |
title_short | Roles of METTL3 in cancer: mechanisms and therapeutic targeting |
title_sort | roles of mettl3 in cancer: mechanisms and therapeutic targeting |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457244/ https://www.ncbi.nlm.nih.gov/pubmed/32854717 http://dx.doi.org/10.1186/s13045-020-00951-w |
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