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p53 mRNA Metabolism Links with the DNA Damage Response
Human cells are subjected to continuous challenges by different genotoxic stress attacks. DNA damage leads to erroneous mutations, which can alter the function of oncogenes or tumor suppressors, resulting in cancer development. To circumvent this, cells activate the DNA damage response (DDR), which...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465283/ https://www.ncbi.nlm.nih.gov/pubmed/34573428 http://dx.doi.org/10.3390/genes12091446 |
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author | Vadivel Gnanasundram, Sivakumar Bonczek, Ondrej Wang, Lixiao Chen, Sa Fahraeus, Robin |
author_facet | Vadivel Gnanasundram, Sivakumar Bonczek, Ondrej Wang, Lixiao Chen, Sa Fahraeus, Robin |
author_sort | Vadivel Gnanasundram, Sivakumar |
collection | PubMed |
description | Human cells are subjected to continuous challenges by different genotoxic stress attacks. DNA damage leads to erroneous mutations, which can alter the function of oncogenes or tumor suppressors, resulting in cancer development. To circumvent this, cells activate the DNA damage response (DDR), which mainly involves cell cycle regulation and DNA repair processes. The tumor suppressor p53 plays a pivotal role in the DDR by halting the cell cycle and facilitating the DNA repair processes. Various pathways and factors participating in the detection and repair of DNA have been described, including scores of RNA-binding proteins (RBPs) and RNAs. It has become increasingly clear that p53’s role is multitasking, and p53 mRNA regulation plays a prominent part in the DDR. This review is aimed at covering the p53 RNA metabolism linked to the DDR and highlights the recent findings. |
format | Online Article Text |
id | pubmed-8465283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84652832021-09-27 p53 mRNA Metabolism Links with the DNA Damage Response Vadivel Gnanasundram, Sivakumar Bonczek, Ondrej Wang, Lixiao Chen, Sa Fahraeus, Robin Genes (Basel) Review Human cells are subjected to continuous challenges by different genotoxic stress attacks. DNA damage leads to erroneous mutations, which can alter the function of oncogenes or tumor suppressors, resulting in cancer development. To circumvent this, cells activate the DNA damage response (DDR), which mainly involves cell cycle regulation and DNA repair processes. The tumor suppressor p53 plays a pivotal role in the DDR by halting the cell cycle and facilitating the DNA repair processes. Various pathways and factors participating in the detection and repair of DNA have been described, including scores of RNA-binding proteins (RBPs) and RNAs. It has become increasingly clear that p53’s role is multitasking, and p53 mRNA regulation plays a prominent part in the DDR. This review is aimed at covering the p53 RNA metabolism linked to the DDR and highlights the recent findings. MDPI 2021-09-20 /pmc/articles/PMC8465283/ /pubmed/34573428 http://dx.doi.org/10.3390/genes12091446 Text en © 2021 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 Vadivel Gnanasundram, Sivakumar Bonczek, Ondrej Wang, Lixiao Chen, Sa Fahraeus, Robin p53 mRNA Metabolism Links with the DNA Damage Response |
title | p53 mRNA Metabolism Links with the DNA Damage Response |
title_full | p53 mRNA Metabolism Links with the DNA Damage Response |
title_fullStr | p53 mRNA Metabolism Links with the DNA Damage Response |
title_full_unstemmed | p53 mRNA Metabolism Links with the DNA Damage Response |
title_short | p53 mRNA Metabolism Links with the DNA Damage Response |
title_sort | p53 mrna metabolism links with the dna damage response |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465283/ https://www.ncbi.nlm.nih.gov/pubmed/34573428 http://dx.doi.org/10.3390/genes12091446 |
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