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Streptococcus mutans promotes tumor progression in oral squamous cell carcinoma
Oral squamous cell carcinoma (OSCC) is an aggressive head and neck cancer. Evidence showed that some pathogenic bacteria are associated with periodontitis and oral cancer. The change in oral microbiome composition and the role of the specific periodontal pathogen Streptococcus mutans in OSCC were in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Ivyspring International Publisher
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516012/ https://www.ncbi.nlm.nih.gov/pubmed/36186905 http://dx.doi.org/10.7150/jca.73310 |
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author | Tsai, Ming-Shao Chen, Yu-Yen Chen, Wen-Cheng Chen, Miao-Fen |
author_facet | Tsai, Ming-Shao Chen, Yu-Yen Chen, Wen-Cheng Chen, Miao-Fen |
author_sort | Tsai, Ming-Shao |
collection | PubMed |
description | Oral squamous cell carcinoma (OSCC) is an aggressive head and neck cancer. Evidence showed that some pathogenic bacteria are associated with periodontitis and oral cancer. The change in oral microbiome composition and the role of the specific periodontal pathogen Streptococcus mutans in OSCC were investigated. We analyzed the microbiome of oral biofilms to identify if the oral microbiome composition was associated with OSCC. The role of S. mutans with clinical prognosis for OSCC was also examined. We further examined the role of S. mutans infection in OSCC progression in preclinical experiments. The microbiome assay by oral biofilms revealed that there was different microbiota composition between OSCC patients and health participants. Furthermore, the microbiota profiles showed that S. mutans abundance was associated with the development of OSCC development. Using the 16S rRNA PCR analysis, the presence of S. mutans was associated with advanced clinical stage and poor disease control. Furthermore, in the 4-nitroquinoline 1-oxide-induced mouse model, the presence of S. mutans was associated with elevated invasive oral cancer incidence. By cellular and xenograft tumor model using oral cancer cells, S. mutans infection was associated with the increased tumor aggressiveness, the epithelial-mesenchymal transition and interleukin-6 (IL-6) production; it also correlated with the recruitment of myeloid-derived-suppressor cells. When IL-6 signaling inhibited, the effects of S. mutans on tumor aggressiveness were attenuated. In conclusion, S. mutans may have the additive effect on oral cancer development and progression. Good oral hygiene to eradicate S. mutans or targeting IL-6 signaling could be a promising strategy for OSCC associated with S.mutans infection. |
format | Online Article Text |
id | pubmed-9516012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-95160122022-09-30 Streptococcus mutans promotes tumor progression in oral squamous cell carcinoma Tsai, Ming-Shao Chen, Yu-Yen Chen, Wen-Cheng Chen, Miao-Fen J Cancer Research Paper Oral squamous cell carcinoma (OSCC) is an aggressive head and neck cancer. Evidence showed that some pathogenic bacteria are associated with periodontitis and oral cancer. The change in oral microbiome composition and the role of the specific periodontal pathogen Streptococcus mutans in OSCC were investigated. We analyzed the microbiome of oral biofilms to identify if the oral microbiome composition was associated with OSCC. The role of S. mutans with clinical prognosis for OSCC was also examined. We further examined the role of S. mutans infection in OSCC progression in preclinical experiments. The microbiome assay by oral biofilms revealed that there was different microbiota composition between OSCC patients and health participants. Furthermore, the microbiota profiles showed that S. mutans abundance was associated with the development of OSCC development. Using the 16S rRNA PCR analysis, the presence of S. mutans was associated with advanced clinical stage and poor disease control. Furthermore, in the 4-nitroquinoline 1-oxide-induced mouse model, the presence of S. mutans was associated with elevated invasive oral cancer incidence. By cellular and xenograft tumor model using oral cancer cells, S. mutans infection was associated with the increased tumor aggressiveness, the epithelial-mesenchymal transition and interleukin-6 (IL-6) production; it also correlated with the recruitment of myeloid-derived-suppressor cells. When IL-6 signaling inhibited, the effects of S. mutans on tumor aggressiveness were attenuated. In conclusion, S. mutans may have the additive effect on oral cancer development and progression. Good oral hygiene to eradicate S. mutans or targeting IL-6 signaling could be a promising strategy for OSCC associated with S.mutans infection. Ivyspring International Publisher 2022-09-21 /pmc/articles/PMC9516012/ /pubmed/36186905 http://dx.doi.org/10.7150/jca.73310 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Tsai, Ming-Shao Chen, Yu-Yen Chen, Wen-Cheng Chen, Miao-Fen Streptococcus mutans promotes tumor progression in oral squamous cell carcinoma |
title | Streptococcus mutans promotes tumor progression in oral squamous cell carcinoma |
title_full | Streptococcus mutans promotes tumor progression in oral squamous cell carcinoma |
title_fullStr | Streptococcus mutans promotes tumor progression in oral squamous cell carcinoma |
title_full_unstemmed | Streptococcus mutans promotes tumor progression in oral squamous cell carcinoma |
title_short | Streptococcus mutans promotes tumor progression in oral squamous cell carcinoma |
title_sort | streptococcus mutans promotes tumor progression in oral squamous cell carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516012/ https://www.ncbi.nlm.nih.gov/pubmed/36186905 http://dx.doi.org/10.7150/jca.73310 |
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