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Microbial Regulation of p53 Tumor Suppressor

p53 tumor suppressor has been identified as a protein interacting with the large T antigen produced by simian vacuolating virus 40 (SV40). Subsequent research on p53 inhibition by SV40 and other tumor viruses has not only helped to gain a better understanding of viral biology, but also shaped our kn...

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Detalles Bibliográficos
Autores principales: Zaika, Alexander I., Wei, Jinxiong, Noto, Jennifer M., Peek, Richard M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574736/
https://www.ncbi.nlm.nih.gov/pubmed/26379246
http://dx.doi.org/10.1371/journal.ppat.1005099
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author Zaika, Alexander I.
Wei, Jinxiong
Noto, Jennifer M.
Peek, Richard M.
author_facet Zaika, Alexander I.
Wei, Jinxiong
Noto, Jennifer M.
Peek, Richard M.
author_sort Zaika, Alexander I.
collection PubMed
description p53 tumor suppressor has been identified as a protein interacting with the large T antigen produced by simian vacuolating virus 40 (SV40). Subsequent research on p53 inhibition by SV40 and other tumor viruses has not only helped to gain a better understanding of viral biology, but also shaped our knowledge of human tumorigenesis. Recent studies have found, however, that inhibition of p53 is not strictly in the realm of viruses. Some bacterial pathogens also actively inhibit p53 protein and induce its degradation, resulting in alteration of cellular stress responses. This phenomenon was initially characterized in gastric epithelial cells infected with Helicobacter pylori, a bacterial pathogen that commonly infects the human stomach and is strongly linked to gastric cancer. Besides H. pylori, a number of other bacterial species were recently discovered to inhibit p53. These findings provide novel insights into host–bacteria interactions and tumorigenesis associated with bacterial infections.
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spelling pubmed-45747362015-09-25 Microbial Regulation of p53 Tumor Suppressor Zaika, Alexander I. Wei, Jinxiong Noto, Jennifer M. Peek, Richard M. PLoS Pathog Review p53 tumor suppressor has been identified as a protein interacting with the large T antigen produced by simian vacuolating virus 40 (SV40). Subsequent research on p53 inhibition by SV40 and other tumor viruses has not only helped to gain a better understanding of viral biology, but also shaped our knowledge of human tumorigenesis. Recent studies have found, however, that inhibition of p53 is not strictly in the realm of viruses. Some bacterial pathogens also actively inhibit p53 protein and induce its degradation, resulting in alteration of cellular stress responses. This phenomenon was initially characterized in gastric epithelial cells infected with Helicobacter pylori, a bacterial pathogen that commonly infects the human stomach and is strongly linked to gastric cancer. Besides H. pylori, a number of other bacterial species were recently discovered to inhibit p53. These findings provide novel insights into host–bacteria interactions and tumorigenesis associated with bacterial infections. Public Library of Science 2015-09-17 /pmc/articles/PMC4574736/ /pubmed/26379246 http://dx.doi.org/10.1371/journal.ppat.1005099 Text en © 2015 Zaika et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Review
Zaika, Alexander I.
Wei, Jinxiong
Noto, Jennifer M.
Peek, Richard M.
Microbial Regulation of p53 Tumor Suppressor
title Microbial Regulation of p53 Tumor Suppressor
title_full Microbial Regulation of p53 Tumor Suppressor
title_fullStr Microbial Regulation of p53 Tumor Suppressor
title_full_unstemmed Microbial Regulation of p53 Tumor Suppressor
title_short Microbial Regulation of p53 Tumor Suppressor
title_sort microbial regulation of p53 tumor suppressor
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574736/
https://www.ncbi.nlm.nih.gov/pubmed/26379246
http://dx.doi.org/10.1371/journal.ppat.1005099
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