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Disruption of the RNA modifications that target the ribosome translation machinery in human cancer
Genetic and epigenetic changes deregulate RNA and protein expression in cancer cells. In this regard, tumors exhibit an abnormal proteome in comparison to the corresponding normal tissues. Translation control is a crucial step in the regulation of gene expression regulation under normal and patholog...
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/PMC7114786/ https://www.ncbi.nlm.nih.gov/pubmed/32241281 http://dx.doi.org/10.1186/s12943-020-01192-8 |
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author | Janin, Maxime Coll-SanMartin, Laia Esteller, Manel |
author_facet | Janin, Maxime Coll-SanMartin, Laia Esteller, Manel |
author_sort | Janin, Maxime |
collection | PubMed |
description | Genetic and epigenetic changes deregulate RNA and protein expression in cancer cells. In this regard, tumors exhibit an abnormal proteome in comparison to the corresponding normal tissues. Translation control is a crucial step in the regulation of gene expression regulation under normal and pathological conditions that ultimately determines cellular fate. In this context, evidence shows that transfer and ribosomal RNA (tRNA and rRNA) modifications affect the efficacy and fidelity of translation. The number of RNA modifications increases with the complexity of organisms, suggesting an evolutionary diversification of the possibilities for fine-tuning the functions of coding and non-coding RNAs. In this review, we focus on alterations of modifications of transfer and ribosomal RNA that affect translation in human cancer. This variation in the RNA modification status can be the result of altered modifier expression (writers, readers or erasers), but also due to components of the machineries (C/D or H/ACA boxes) or alterations of proteins involved in modifier expression. Broadening our understanding of the mechanisms by which site-specific modifications modulate ribosome activity in the context of tumorigenesis will enable us to enrich our knowledge about how ribosomes can influence cell fate and form the basis of new therapeutic opportunities. |
format | Online Article Text |
id | pubmed-7114786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71147862020-04-07 Disruption of the RNA modifications that target the ribosome translation machinery in human cancer Janin, Maxime Coll-SanMartin, Laia Esteller, Manel Mol Cancer Review Genetic and epigenetic changes deregulate RNA and protein expression in cancer cells. In this regard, tumors exhibit an abnormal proteome in comparison to the corresponding normal tissues. Translation control is a crucial step in the regulation of gene expression regulation under normal and pathological conditions that ultimately determines cellular fate. In this context, evidence shows that transfer and ribosomal RNA (tRNA and rRNA) modifications affect the efficacy and fidelity of translation. The number of RNA modifications increases with the complexity of organisms, suggesting an evolutionary diversification of the possibilities for fine-tuning the functions of coding and non-coding RNAs. In this review, we focus on alterations of modifications of transfer and ribosomal RNA that affect translation in human cancer. This variation in the RNA modification status can be the result of altered modifier expression (writers, readers or erasers), but also due to components of the machineries (C/D or H/ACA boxes) or alterations of proteins involved in modifier expression. Broadening our understanding of the mechanisms by which site-specific modifications modulate ribosome activity in the context of tumorigenesis will enable us to enrich our knowledge about how ribosomes can influence cell fate and form the basis of new therapeutic opportunities. BioMed Central 2020-04-02 /pmc/articles/PMC7114786/ /pubmed/32241281 http://dx.doi.org/10.1186/s12943-020-01192-8 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 Janin, Maxime Coll-SanMartin, Laia Esteller, Manel Disruption of the RNA modifications that target the ribosome translation machinery in human cancer |
title | Disruption of the RNA modifications that target the ribosome translation machinery in human cancer |
title_full | Disruption of the RNA modifications that target the ribosome translation machinery in human cancer |
title_fullStr | Disruption of the RNA modifications that target the ribosome translation machinery in human cancer |
title_full_unstemmed | Disruption of the RNA modifications that target the ribosome translation machinery in human cancer |
title_short | Disruption of the RNA modifications that target the ribosome translation machinery in human cancer |
title_sort | disruption of the rna modifications that target the ribosome translation machinery in human cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114786/ https://www.ncbi.nlm.nih.gov/pubmed/32241281 http://dx.doi.org/10.1186/s12943-020-01192-8 |
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