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Enterobacteria impair host p53 tumor suppressor activity through mRNA destabilization
Increasing evidence highlights the role of bacteria in the physiopathology of cancer. However, the underlying molecular mechanisms remains poorly understood. Several cancer-associated bacteria have been shown to produce toxins which interfere with the host defense against tumorigenesis. Here, we sho...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993692/ https://www.ncbi.nlm.nih.gov/pubmed/35197571 http://dx.doi.org/10.1038/s41388-022-02238-5 |
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author | Aschtgen, Marie-Stéphanie Fragkoulis, Konstantinos Sanz, Gema Normark, Staffan Selivanova, Galina Henriques-Normark, Birgitta Peuget, Sylvain |
author_facet | Aschtgen, Marie-Stéphanie Fragkoulis, Konstantinos Sanz, Gema Normark, Staffan Selivanova, Galina Henriques-Normark, Birgitta Peuget, Sylvain |
author_sort | Aschtgen, Marie-Stéphanie |
collection | PubMed |
description | Increasing evidence highlights the role of bacteria in the physiopathology of cancer. However, the underlying molecular mechanisms remains poorly understood. Several cancer-associated bacteria have been shown to produce toxins which interfere with the host defense against tumorigenesis. Here, we show that lipopolysaccharides from Klebsiella pneumoniae and other Enterobacteria strongly inhibit the host tumor suppressor p53 pathway through a novel mechanism of p53 regulation. We found that lipopolysaccharides destabilize TP53 mRNA through a TLR4-NF-κB-mediated inhibition of the RNA-binding factor Wig-1. Importantly, we show that K. pneumoniae disables two major tumor barriers, oncogene-induced DNA damage signaling and senescence, by impairing p53 transcriptional activity upon DNA damage and oncogenic stress. Furthermore, we found an inverse correlation between the levels of TLR4 and p53 mutation in colorectal tumors. Hence, our data suggest that the repression of p53 by Enterobacteria via TLR4 alleviates the selection pressure for p53 oncogenic mutations and shapes the genomic evolution of cancer. |
format | Online Article Text |
id | pubmed-8993692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89936922022-04-22 Enterobacteria impair host p53 tumor suppressor activity through mRNA destabilization Aschtgen, Marie-Stéphanie Fragkoulis, Konstantinos Sanz, Gema Normark, Staffan Selivanova, Galina Henriques-Normark, Birgitta Peuget, Sylvain Oncogene Article Increasing evidence highlights the role of bacteria in the physiopathology of cancer. However, the underlying molecular mechanisms remains poorly understood. Several cancer-associated bacteria have been shown to produce toxins which interfere with the host defense against tumorigenesis. Here, we show that lipopolysaccharides from Klebsiella pneumoniae and other Enterobacteria strongly inhibit the host tumor suppressor p53 pathway through a novel mechanism of p53 regulation. We found that lipopolysaccharides destabilize TP53 mRNA through a TLR4-NF-κB-mediated inhibition of the RNA-binding factor Wig-1. Importantly, we show that K. pneumoniae disables two major tumor barriers, oncogene-induced DNA damage signaling and senescence, by impairing p53 transcriptional activity upon DNA damage and oncogenic stress. Furthermore, we found an inverse correlation between the levels of TLR4 and p53 mutation in colorectal tumors. Hence, our data suggest that the repression of p53 by Enterobacteria via TLR4 alleviates the selection pressure for p53 oncogenic mutations and shapes the genomic evolution of cancer. Nature Publishing Group UK 2022-02-23 2022 /pmc/articles/PMC8993692/ /pubmed/35197571 http://dx.doi.org/10.1038/s41388-022-02238-5 Text en © The Author(s) 2022 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Aschtgen, Marie-Stéphanie Fragkoulis, Konstantinos Sanz, Gema Normark, Staffan Selivanova, Galina Henriques-Normark, Birgitta Peuget, Sylvain Enterobacteria impair host p53 tumor suppressor activity through mRNA destabilization |
title | Enterobacteria impair host p53 tumor suppressor activity through mRNA destabilization |
title_full | Enterobacteria impair host p53 tumor suppressor activity through mRNA destabilization |
title_fullStr | Enterobacteria impair host p53 tumor suppressor activity through mRNA destabilization |
title_full_unstemmed | Enterobacteria impair host p53 tumor suppressor activity through mRNA destabilization |
title_short | Enterobacteria impair host p53 tumor suppressor activity through mRNA destabilization |
title_sort | enterobacteria impair host p53 tumor suppressor activity through mrna destabilization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993692/ https://www.ncbi.nlm.nih.gov/pubmed/35197571 http://dx.doi.org/10.1038/s41388-022-02238-5 |
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