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Critical Roles of METTL3 in Translation Regulation of Cancer
Aberrant translation, a characteristic feature of cancer, is regulated by the complex and sophisticated RNA binding proteins (RBPs) in the canonical translation machinery. N6-methyladenosine (m(6)A) modifications are the most abundant internal modifications in mRNAs mediated by methyltransferase-lik...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953158/ https://www.ncbi.nlm.nih.gov/pubmed/36830614 http://dx.doi.org/10.3390/biom13020243 |
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author | Meng, Wangyang Xiao, Han Mei, Peiyuan Chen, Jiaping Wang, Yangwei Zhao, Rong Liao, Yongde |
author_facet | Meng, Wangyang Xiao, Han Mei, Peiyuan Chen, Jiaping Wang, Yangwei Zhao, Rong Liao, Yongde |
author_sort | Meng, Wangyang |
collection | PubMed |
description | Aberrant translation, a characteristic feature of cancer, is regulated by the complex and sophisticated RNA binding proteins (RBPs) in the canonical translation machinery. N6-methyladenosine (m(6)A) modifications are the most abundant internal modifications in mRNAs mediated by methyltransferase-like 3 (METTL3). METTL3 is commonly aberrantly expressed in different tumors and affects the mRNA translation of many oncogenes or dysregulated tumor suppressor genes in a variety of ways. In this review, we discuss the critical roles of METTL3 in translation regulation and how METTL3 and m(6)A reader proteins in collaboration with RBPs within the canonical translation machinery promote aberrant translation in tumorigenesis, providing an overview of recent efforts aiming to ‘translate’ these results to the clinic. |
format | Online Article Text |
id | pubmed-9953158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99531582023-02-25 Critical Roles of METTL3 in Translation Regulation of Cancer Meng, Wangyang Xiao, Han Mei, Peiyuan Chen, Jiaping Wang, Yangwei Zhao, Rong Liao, Yongde Biomolecules Review Aberrant translation, a characteristic feature of cancer, is regulated by the complex and sophisticated RNA binding proteins (RBPs) in the canonical translation machinery. N6-methyladenosine (m(6)A) modifications are the most abundant internal modifications in mRNAs mediated by methyltransferase-like 3 (METTL3). METTL3 is commonly aberrantly expressed in different tumors and affects the mRNA translation of many oncogenes or dysregulated tumor suppressor genes in a variety of ways. In this review, we discuss the critical roles of METTL3 in translation regulation and how METTL3 and m(6)A reader proteins in collaboration with RBPs within the canonical translation machinery promote aberrant translation in tumorigenesis, providing an overview of recent efforts aiming to ‘translate’ these results to the clinic. MDPI 2023-01-27 /pmc/articles/PMC9953158/ /pubmed/36830614 http://dx.doi.org/10.3390/biom13020243 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Meng, Wangyang Xiao, Han Mei, Peiyuan Chen, Jiaping Wang, Yangwei Zhao, Rong Liao, Yongde Critical Roles of METTL3 in Translation Regulation of Cancer |
title | Critical Roles of METTL3 in Translation Regulation of Cancer |
title_full | Critical Roles of METTL3 in Translation Regulation of Cancer |
title_fullStr | Critical Roles of METTL3 in Translation Regulation of Cancer |
title_full_unstemmed | Critical Roles of METTL3 in Translation Regulation of Cancer |
title_short | Critical Roles of METTL3 in Translation Regulation of Cancer |
title_sort | critical roles of mettl3 in translation regulation of cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953158/ https://www.ncbi.nlm.nih.gov/pubmed/36830614 http://dx.doi.org/10.3390/biom13020243 |
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