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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...

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Autores principales: Aschtgen, Marie-Stéphanie, Fragkoulis, Konstantinos, Sanz, Gema, Normark, Staffan, Selivanova, Galina, Henriques-Normark, Birgitta, Peuget, Sylvain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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.
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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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