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Dysbiosis of Oral Microbiota During Oral Squamous Cell Carcinoma Development
Infection with specific pathogens and alterations in tissue commensal microbial composition are intricately associated with the development of many human cancers. Likewise, dysbiosis of oral microbiome was also shown to play critical role in the initiation as well as progression of oral cancer. Howe...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940518/ https://www.ncbi.nlm.nih.gov/pubmed/33708627 http://dx.doi.org/10.3389/fonc.2021.614448 |
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author | Sarkar, Purandar Malik, Samaresh Laha, Sayantan Das, Shantanab Bunk, Soumya Ray, Jay Gopal Chatterjee, Raghunath Saha, Abhik |
author_facet | Sarkar, Purandar Malik, Samaresh Laha, Sayantan Das, Shantanab Bunk, Soumya Ray, Jay Gopal Chatterjee, Raghunath Saha, Abhik |
author_sort | Sarkar, Purandar |
collection | PubMed |
description | Infection with specific pathogens and alterations in tissue commensal microbial composition are intricately associated with the development of many human cancers. Likewise, dysbiosis of oral microbiome was also shown to play critical role in the initiation as well as progression of oral cancer. However, there are no reports portraying changes in oral microbial community in the patients of Indian subcontinent, which has the highest incidence of oral cancer per year, globally. To establish the association of bacterial dysbiosis and oral squamous cell carcinoma (OSCC) among the Indian population, malignant lesions and anatomically matched adjacent normal tissues were obtained from fifty well-differentiated OSCC patients and analyzed using 16S rRNA V3-V4 amplicon based sequencing on the MiSeq platform. Interestingly, in contrast to the previous studies, a significantly lower bacterial diversity was observed in the malignant samples as compared to the normal counterpart. Overall our study identified Prevotella, Corynebacterium, Pseudomonas, Deinococcus and Noviherbaspirillum as significantly enriched genera, whereas genera including Actinomyces, Sutterella, Stenotrophomonas, Anoxybacillus, and Serratia were notably decreased in the OSCC lesions. Moreover, we demonstrated HPV-16 but not HPV-18 was significantly associated with the OSCC development. In future, with additional validation, this panel could directly be applied into clinical diagnostic and prognostic workflows for OSCC in Indian scenario. |
format | Online Article Text |
id | pubmed-7940518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79405182021-03-10 Dysbiosis of Oral Microbiota During Oral Squamous Cell Carcinoma Development Sarkar, Purandar Malik, Samaresh Laha, Sayantan Das, Shantanab Bunk, Soumya Ray, Jay Gopal Chatterjee, Raghunath Saha, Abhik Front Oncol Oncology Infection with specific pathogens and alterations in tissue commensal microbial composition are intricately associated with the development of many human cancers. Likewise, dysbiosis of oral microbiome was also shown to play critical role in the initiation as well as progression of oral cancer. However, there are no reports portraying changes in oral microbial community in the patients of Indian subcontinent, which has the highest incidence of oral cancer per year, globally. To establish the association of bacterial dysbiosis and oral squamous cell carcinoma (OSCC) among the Indian population, malignant lesions and anatomically matched adjacent normal tissues were obtained from fifty well-differentiated OSCC patients and analyzed using 16S rRNA V3-V4 amplicon based sequencing on the MiSeq platform. Interestingly, in contrast to the previous studies, a significantly lower bacterial diversity was observed in the malignant samples as compared to the normal counterpart. Overall our study identified Prevotella, Corynebacterium, Pseudomonas, Deinococcus and Noviherbaspirillum as significantly enriched genera, whereas genera including Actinomyces, Sutterella, Stenotrophomonas, Anoxybacillus, and Serratia were notably decreased in the OSCC lesions. Moreover, we demonstrated HPV-16 but not HPV-18 was significantly associated with the OSCC development. In future, with additional validation, this panel could directly be applied into clinical diagnostic and prognostic workflows for OSCC in Indian scenario. Frontiers Media S.A. 2021-02-23 /pmc/articles/PMC7940518/ /pubmed/33708627 http://dx.doi.org/10.3389/fonc.2021.614448 Text en Copyright © 2021 Sarkar, Malik, Laha, Das, Bunk, Ray, Chatterjee and Saha http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Sarkar, Purandar Malik, Samaresh Laha, Sayantan Das, Shantanab Bunk, Soumya Ray, Jay Gopal Chatterjee, Raghunath Saha, Abhik Dysbiosis of Oral Microbiota During Oral Squamous Cell Carcinoma Development |
title | Dysbiosis of Oral Microbiota During Oral Squamous Cell Carcinoma Development |
title_full | Dysbiosis of Oral Microbiota During Oral Squamous Cell Carcinoma Development |
title_fullStr | Dysbiosis of Oral Microbiota During Oral Squamous Cell Carcinoma Development |
title_full_unstemmed | Dysbiosis of Oral Microbiota During Oral Squamous Cell Carcinoma Development |
title_short | Dysbiosis of Oral Microbiota During Oral Squamous Cell Carcinoma Development |
title_sort | dysbiosis of oral microbiota during oral squamous cell carcinoma development |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940518/ https://www.ncbi.nlm.nih.gov/pubmed/33708627 http://dx.doi.org/10.3389/fonc.2021.614448 |
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