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Oral Microbiota from Periodontitis Promote Oral Squamous Cell Carcinoma Development via γδ T Cell Activation

Oral squamous cell carcinoma (OSCC) is a fatal disease, and periodontitis is associated with OSCC development. However, the pathogenesis in the context of OSCC with periodontitis has not been fully understood. Here, we demonstrated that periodontitis promoted OSCC development, accompanied by alterat...

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Autores principales: Wei, Wei, Li, Jia, Shen, Xin, Lyu, Jinglu, Yan, Caixia, Tang, Boyu, Ma, Wenjuan, Xie, Huixu, Zhao, Lei, Cheng, Lei, Deng, Ye, Li, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600543/
https://www.ncbi.nlm.nih.gov/pubmed/36000726
http://dx.doi.org/10.1128/msystems.00469-22
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author Wei, Wei
Li, Jia
Shen, Xin
Lyu, Jinglu
Yan, Caixia
Tang, Boyu
Ma, Wenjuan
Xie, Huixu
Zhao, Lei
Cheng, Lei
Deng, Ye
Li, Yan
author_facet Wei, Wei
Li, Jia
Shen, Xin
Lyu, Jinglu
Yan, Caixia
Tang, Boyu
Ma, Wenjuan
Xie, Huixu
Zhao, Lei
Cheng, Lei
Deng, Ye
Li, Yan
author_sort Wei, Wei
collection PubMed
description Oral squamous cell carcinoma (OSCC) is a fatal disease, and periodontitis is associated with OSCC development. However, the pathogenesis in the context of OSCC with periodontitis has not been fully understood. Here, we demonstrated that periodontitis promoted OSCC development, accompanied by alterations in the oral bacterial community and the tumor immune microenvironment. The oral microbiota from periodontitis maintained the dominant position throughout the whole process of OSCC with periodontitis, of which Porphyromonas was the most abundant genus. The oral microbiota from periodontitis could activate interleukin-17-positive (IL-17(+)) γδ T cells directly. The activated γδ T cells were necessary for the IL-17/signal transducer and activator of transcription 3 (STAT3) pathway and promoted M2-tumor-associated macrophage (TAM) infiltration in OSCC proliferation. Our data provide insight into the carcinogenesis of OSCC with periodontitis by outlining the tumor-associated immune response shaped by the oral microbiota from periodontitis. Thus, oral commensal bacteria and IL-17(+) γδ T cells might be potential targets for monitoring and treating OSCC. IMPORTANCE The work reveals the role of the oral microbiota from periodontitis in carcinogenesis. Furthermore, our study provides insight into the pathogenesis of OSCC with periodontitis by outlining the tumor-associated immune response shaped by the oral microbiota from periodontitis, which might identify new research and intervention targets for OSCC with periodontitis.
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spelling pubmed-96005432022-10-27 Oral Microbiota from Periodontitis Promote Oral Squamous Cell Carcinoma Development via γδ T Cell Activation Wei, Wei Li, Jia Shen, Xin Lyu, Jinglu Yan, Caixia Tang, Boyu Ma, Wenjuan Xie, Huixu Zhao, Lei Cheng, Lei Deng, Ye Li, Yan mSystems Research Article Oral squamous cell carcinoma (OSCC) is a fatal disease, and periodontitis is associated with OSCC development. However, the pathogenesis in the context of OSCC with periodontitis has not been fully understood. Here, we demonstrated that periodontitis promoted OSCC development, accompanied by alterations in the oral bacterial community and the tumor immune microenvironment. The oral microbiota from periodontitis maintained the dominant position throughout the whole process of OSCC with periodontitis, of which Porphyromonas was the most abundant genus. The oral microbiota from periodontitis could activate interleukin-17-positive (IL-17(+)) γδ T cells directly. The activated γδ T cells were necessary for the IL-17/signal transducer and activator of transcription 3 (STAT3) pathway and promoted M2-tumor-associated macrophage (TAM) infiltration in OSCC proliferation. Our data provide insight into the carcinogenesis of OSCC with periodontitis by outlining the tumor-associated immune response shaped by the oral microbiota from periodontitis. Thus, oral commensal bacteria and IL-17(+) γδ T cells might be potential targets for monitoring and treating OSCC. IMPORTANCE The work reveals the role of the oral microbiota from periodontitis in carcinogenesis. Furthermore, our study provides insight into the pathogenesis of OSCC with periodontitis by outlining the tumor-associated immune response shaped by the oral microbiota from periodontitis, which might identify new research and intervention targets for OSCC with periodontitis. American Society for Microbiology 2022-08-24 /pmc/articles/PMC9600543/ /pubmed/36000726 http://dx.doi.org/10.1128/msystems.00469-22 Text en Copyright © 2022 Wei et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Wei, Wei
Li, Jia
Shen, Xin
Lyu, Jinglu
Yan, Caixia
Tang, Boyu
Ma, Wenjuan
Xie, Huixu
Zhao, Lei
Cheng, Lei
Deng, Ye
Li, Yan
Oral Microbiota from Periodontitis Promote Oral Squamous Cell Carcinoma Development via γδ T Cell Activation
title Oral Microbiota from Periodontitis Promote Oral Squamous Cell Carcinoma Development via γδ T Cell Activation
title_full Oral Microbiota from Periodontitis Promote Oral Squamous Cell Carcinoma Development via γδ T Cell Activation
title_fullStr Oral Microbiota from Periodontitis Promote Oral Squamous Cell Carcinoma Development via γδ T Cell Activation
title_full_unstemmed Oral Microbiota from Periodontitis Promote Oral Squamous Cell Carcinoma Development via γδ T Cell Activation
title_short Oral Microbiota from Periodontitis Promote Oral Squamous Cell Carcinoma Development via γδ T Cell Activation
title_sort oral microbiota from periodontitis promote oral squamous cell carcinoma development via γδ t cell activation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600543/
https://www.ncbi.nlm.nih.gov/pubmed/36000726
http://dx.doi.org/10.1128/msystems.00469-22
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