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An old friend with a new face: tRNA-derived small RNAs with big regulatory potential in cancer biology
Transfer RNAs (tRNAs) are small non-coding RNAs (sncRNAs) essential for protein translation. Emerging evidence suggests that tRNAs can also be processed into smaller fragments, tRNA-derived small RNAs (tsRNAs), a novel class of sncRNAs with powerful applications and high biological relevance to canc...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133234/ https://www.ncbi.nlm.nih.gov/pubmed/36759729 http://dx.doi.org/10.1038/s41416-023-02191-4 |
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author | Di Fazio, Arianna Gullerova, Monika |
author_facet | Di Fazio, Arianna Gullerova, Monika |
author_sort | Di Fazio, Arianna |
collection | PubMed |
description | Transfer RNAs (tRNAs) are small non-coding RNAs (sncRNAs) essential for protein translation. Emerging evidence suggests that tRNAs can also be processed into smaller fragments, tRNA-derived small RNAs (tsRNAs), a novel class of sncRNAs with powerful applications and high biological relevance to cancer. tsRNAs biogenesis is heterogeneous and involves different ribonucleases, such as Angiogenin and Dicer. For many years, tsRNAs were thought to be just degradation products. However, accumulating evidence shows their roles in gene expression: either directly via destabilising the mRNA or the ribosomal machinery, or indirectly via regulating the expression of ribosomal components. Furthermore, tsRNAs participate in various biological processes linked to cancer, including apoptosis, cell cycle, immune response, and retroviral insertion into the human genome. It is emerging that tsRNAs have significant therapeutic potential. Endogenous tsRNAs can be used as cancer biomarkers, while synthetic tsRNAs and antisense oligonucleotides can be employed to regulate gene expression. In this review, we are recapitulating the regulatory roles of tsRNAs, with a focus on cancer biology. |
format | Online Article Text |
id | pubmed-10133234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101332342023-04-28 An old friend with a new face: tRNA-derived small RNAs with big regulatory potential in cancer biology Di Fazio, Arianna Gullerova, Monika Br J Cancer Review Article Transfer RNAs (tRNAs) are small non-coding RNAs (sncRNAs) essential for protein translation. Emerging evidence suggests that tRNAs can also be processed into smaller fragments, tRNA-derived small RNAs (tsRNAs), a novel class of sncRNAs with powerful applications and high biological relevance to cancer. tsRNAs biogenesis is heterogeneous and involves different ribonucleases, such as Angiogenin and Dicer. For many years, tsRNAs were thought to be just degradation products. However, accumulating evidence shows their roles in gene expression: either directly via destabilising the mRNA or the ribosomal machinery, or indirectly via regulating the expression of ribosomal components. Furthermore, tsRNAs participate in various biological processes linked to cancer, including apoptosis, cell cycle, immune response, and retroviral insertion into the human genome. It is emerging that tsRNAs have significant therapeutic potential. Endogenous tsRNAs can be used as cancer biomarkers, while synthetic tsRNAs and antisense oligonucleotides can be employed to regulate gene expression. In this review, we are recapitulating the regulatory roles of tsRNAs, with a focus on cancer biology. Nature Publishing Group UK 2023-02-09 2023-05-18 /pmc/articles/PMC10133234/ /pubmed/36759729 http://dx.doi.org/10.1038/s41416-023-02191-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Review Article Di Fazio, Arianna Gullerova, Monika An old friend with a new face: tRNA-derived small RNAs with big regulatory potential in cancer biology |
title | An old friend with a new face: tRNA-derived small RNAs with big regulatory potential in cancer biology |
title_full | An old friend with a new face: tRNA-derived small RNAs with big regulatory potential in cancer biology |
title_fullStr | An old friend with a new face: tRNA-derived small RNAs with big regulatory potential in cancer biology |
title_full_unstemmed | An old friend with a new face: tRNA-derived small RNAs with big regulatory potential in cancer biology |
title_short | An old friend with a new face: tRNA-derived small RNAs with big regulatory potential in cancer biology |
title_sort | old friend with a new face: trna-derived small rnas with big regulatory potential in cancer biology |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133234/ https://www.ncbi.nlm.nih.gov/pubmed/36759729 http://dx.doi.org/10.1038/s41416-023-02191-4 |
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