Cargando…
The oral cancer microbiome contains tumor space–specific and clinicopathology-specific bacteria
The crosstalk between the oral microbiome and oral cancer has yet to be characterized. This study recruited 218 patients for clinicopathological data analysis. Multiple types of specimens were collected from 27 patients for 16S rRNA gene sequencing, including 26 saliva, 16 swabs from the surface of...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831678/ https://www.ncbi.nlm.nih.gov/pubmed/36636719 http://dx.doi.org/10.3389/fcimb.2022.942328 |
_version_ | 1784867896000774144 |
---|---|
author | Zeng, Bin Tan, Jun Guo, Guangliang Li, Zhengshi Yang, Le Lao, Xiaomei Wang, Dikan Ma, Jingxin Zhang, Sien Liao, Guiqing Liang, Yujie |
author_facet | Zeng, Bin Tan, Jun Guo, Guangliang Li, Zhengshi Yang, Le Lao, Xiaomei Wang, Dikan Ma, Jingxin Zhang, Sien Liao, Guiqing Liang, Yujie |
author_sort | Zeng, Bin |
collection | PubMed |
description | The crosstalk between the oral microbiome and oral cancer has yet to be characterized. This study recruited 218 patients for clinicopathological data analysis. Multiple types of specimens were collected from 27 patients for 16S rRNA gene sequencing, including 26 saliva, 16 swabs from the surface of tumor tissues, 16 adjacent normal tissues, 22 tumor outer tissue, 22 tumor inner tissues, and 10 lymph nodes. Clinicopathological data showed that the pathogenic bacteria could be frequently detected in the oral cavity of oral cancer patients, which was positively related to diabetes, later T stage of the tumor, and the presence of cervical lymphatic metastasis. Sequencing data revealed that compared with adjacent normal tissues, the microbiome of outer tumor tissues had a greater alpha diversity, with a larger proportion of Fusobacterium, Prevotella, and Porphyromonas, while a smaller proportion of Streptococcus. The space-specific microbiome, comparing outer tumor tissues with inner tumor tissues, suggested minor differences in diversity. However, Fusobacterium, Neisseria, Porphyromonas, and Alloprevotella were more abundant in outer tumor tissues, while Prevotella, Selenomonas, and Parvimonas were enriched in inner tumor tissues. Clinicopathology-specific microbiome analysis found that the diversity was markedly different between negative and positive extranodal extensions, whereas the diversity between different T-stages and N-stages was slightly different. Gemella and Bacillales were enriched in T1/T2-stage patients and the non-lymphatic metastasis group, while Spirochaetae and Flavobacteriia were enriched in the extranodal extension negative group. Taken together, high-throughput DNA sequencing in combination with clinicopathological features facilitated us to characterize special patterns of oral tumor microbiome in different disease developmental stages. |
format | Online Article Text |
id | pubmed-9831678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98316782023-01-11 The oral cancer microbiome contains tumor space–specific and clinicopathology-specific bacteria Zeng, Bin Tan, Jun Guo, Guangliang Li, Zhengshi Yang, Le Lao, Xiaomei Wang, Dikan Ma, Jingxin Zhang, Sien Liao, Guiqing Liang, Yujie Front Cell Infect Microbiol Cellular and Infection Microbiology The crosstalk between the oral microbiome and oral cancer has yet to be characterized. This study recruited 218 patients for clinicopathological data analysis. Multiple types of specimens were collected from 27 patients for 16S rRNA gene sequencing, including 26 saliva, 16 swabs from the surface of tumor tissues, 16 adjacent normal tissues, 22 tumor outer tissue, 22 tumor inner tissues, and 10 lymph nodes. Clinicopathological data showed that the pathogenic bacteria could be frequently detected in the oral cavity of oral cancer patients, which was positively related to diabetes, later T stage of the tumor, and the presence of cervical lymphatic metastasis. Sequencing data revealed that compared with adjacent normal tissues, the microbiome of outer tumor tissues had a greater alpha diversity, with a larger proportion of Fusobacterium, Prevotella, and Porphyromonas, while a smaller proportion of Streptococcus. The space-specific microbiome, comparing outer tumor tissues with inner tumor tissues, suggested minor differences in diversity. However, Fusobacterium, Neisseria, Porphyromonas, and Alloprevotella were more abundant in outer tumor tissues, while Prevotella, Selenomonas, and Parvimonas were enriched in inner tumor tissues. Clinicopathology-specific microbiome analysis found that the diversity was markedly different between negative and positive extranodal extensions, whereas the diversity between different T-stages and N-stages was slightly different. Gemella and Bacillales were enriched in T1/T2-stage patients and the non-lymphatic metastasis group, while Spirochaetae and Flavobacteriia were enriched in the extranodal extension negative group. Taken together, high-throughput DNA sequencing in combination with clinicopathological features facilitated us to characterize special patterns of oral tumor microbiome in different disease developmental stages. Frontiers Media S.A. 2022-12-27 /pmc/articles/PMC9831678/ /pubmed/36636719 http://dx.doi.org/10.3389/fcimb.2022.942328 Text en Copyright © 2022 Zeng, Tan, Guo, Li, Yang, Lao, Wang, Ma, Zhang, Liao and Liang https://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 | Cellular and Infection Microbiology Zeng, Bin Tan, Jun Guo, Guangliang Li, Zhengshi Yang, Le Lao, Xiaomei Wang, Dikan Ma, Jingxin Zhang, Sien Liao, Guiqing Liang, Yujie The oral cancer microbiome contains tumor space–specific and clinicopathology-specific bacteria |
title | The oral cancer microbiome contains tumor space–specific and clinicopathology-specific bacteria |
title_full | The oral cancer microbiome contains tumor space–specific and clinicopathology-specific bacteria |
title_fullStr | The oral cancer microbiome contains tumor space–specific and clinicopathology-specific bacteria |
title_full_unstemmed | The oral cancer microbiome contains tumor space–specific and clinicopathology-specific bacteria |
title_short | The oral cancer microbiome contains tumor space–specific and clinicopathology-specific bacteria |
title_sort | oral cancer microbiome contains tumor space–specific and clinicopathology-specific bacteria |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831678/ https://www.ncbi.nlm.nih.gov/pubmed/36636719 http://dx.doi.org/10.3389/fcimb.2022.942328 |
work_keys_str_mv | AT zengbin theoralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT tanjun theoralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT guoguangliang theoralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT lizhengshi theoralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT yangle theoralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT laoxiaomei theoralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT wangdikan theoralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT majingxin theoralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT zhangsien theoralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT liaoguiqing theoralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT liangyujie theoralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT zengbin oralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT tanjun oralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT guoguangliang oralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT lizhengshi oralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT yangle oralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT laoxiaomei oralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT wangdikan oralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT majingxin oralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT zhangsien oralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT liaoguiqing oralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria AT liangyujie oralcancermicrobiomecontainstumorspacespecificandclinicopathologyspecificbacteria |