Cargando…
The airway microbiota of non‐small cell lung cancer patients and its relationship to tumor stage and EGFR gene mutation
BACKGROUND: Accumulating studies have suggested the airway microbiota in lung cancer patients is significantly different from that of healthy controls. However, little is known about the relationship between airway microbiota and important clinical parameters of lung cancer. In this study, we aimed...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930493/ https://www.ncbi.nlm.nih.gov/pubmed/35142041 http://dx.doi.org/10.1111/1759-7714.14340 |
_version_ | 1784671072587612160 |
---|---|
author | Huang, Dan Hui He, Jing Su, Xiao Fang Wen, Ya Na Zhang, Shu Jia Liu, Lai Yu Zhao, Haijin Ye, Cui Pin Wu, Jian Hua Cai, Shaoxi Dong, Hangming |
author_facet | Huang, Dan Hui He, Jing Su, Xiao Fang Wen, Ya Na Zhang, Shu Jia Liu, Lai Yu Zhao, Haijin Ye, Cui Pin Wu, Jian Hua Cai, Shaoxi Dong, Hangming |
author_sort | Huang, Dan Hui |
collection | PubMed |
description | BACKGROUND: Accumulating studies have suggested the airway microbiota in lung cancer patients is significantly different from that of healthy controls. However, little is known about the relationship between airway microbiota and important clinical parameters of lung cancer. In this study, we aimed to explore the association between sputum microbiota and lung cancer stage, lymph node metastasis, intrathoracic metastasis, and epidermal growth factor receptor (EGFR) gene mutation. METHODS: The microbiota of sputum samples from 85 newly‐diagnosed NSCLC patients were sequenced via 16S rRNA sequencing of the V3–V4 region. Sequencing reads were filtered using QIIME2 and clustered against UPARSE. RESULTS: Alpha‐ and β‐diversity was significantly different between patients in stages I to II (early stage, ES) and patients in stages III to IV (advanced stage, AS). Linear discriminant analysis Effect Size (LEfSe) identified that genera Granulicatella and Actinobacillus were significantly enriched in ES, and the genus Actinomyces was significantly enriched in AS. PICRUSt2 identified that the NAD salvage pathway was significantly enriched in AS, which was positively associated with Granulicatella. Patients with intrathoracic metastasis were associated with increased genus Peptostreptococcus and incomplete reductive TCA cycle, which was associated with increased Peptostreptococcus. Genera Parvimonas, Pseudomona and L‐valine biosynthesis were positively associated with lymph node metastasis. L‐valine biosynthesis was related with increased Pseudomona. Finally, the genus Parvimonas was significantly enriched in adenocarcinoma patients with EGFR mutation. CONCLUSION: The taxonomy structure differed between different lung cancer stages. The tumor stage, intrathoracic metastasis, lymph node metastasis, and EGFR mutation were associated with alteration of specific airway genera and metabolic function of sputum microbiota. |
format | Online Article Text |
id | pubmed-8930493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-89304932022-03-24 The airway microbiota of non‐small cell lung cancer patients and its relationship to tumor stage and EGFR gene mutation Huang, Dan Hui He, Jing Su, Xiao Fang Wen, Ya Na Zhang, Shu Jia Liu, Lai Yu Zhao, Haijin Ye, Cui Pin Wu, Jian Hua Cai, Shaoxi Dong, Hangming Thorac Cancer Original Articles BACKGROUND: Accumulating studies have suggested the airway microbiota in lung cancer patients is significantly different from that of healthy controls. However, little is known about the relationship between airway microbiota and important clinical parameters of lung cancer. In this study, we aimed to explore the association between sputum microbiota and lung cancer stage, lymph node metastasis, intrathoracic metastasis, and epidermal growth factor receptor (EGFR) gene mutation. METHODS: The microbiota of sputum samples from 85 newly‐diagnosed NSCLC patients were sequenced via 16S rRNA sequencing of the V3–V4 region. Sequencing reads were filtered using QIIME2 and clustered against UPARSE. RESULTS: Alpha‐ and β‐diversity was significantly different between patients in stages I to II (early stage, ES) and patients in stages III to IV (advanced stage, AS). Linear discriminant analysis Effect Size (LEfSe) identified that genera Granulicatella and Actinobacillus were significantly enriched in ES, and the genus Actinomyces was significantly enriched in AS. PICRUSt2 identified that the NAD salvage pathway was significantly enriched in AS, which was positively associated with Granulicatella. Patients with intrathoracic metastasis were associated with increased genus Peptostreptococcus and incomplete reductive TCA cycle, which was associated with increased Peptostreptococcus. Genera Parvimonas, Pseudomona and L‐valine biosynthesis were positively associated with lymph node metastasis. L‐valine biosynthesis was related with increased Pseudomona. Finally, the genus Parvimonas was significantly enriched in adenocarcinoma patients with EGFR mutation. CONCLUSION: The taxonomy structure differed between different lung cancer stages. The tumor stage, intrathoracic metastasis, lymph node metastasis, and EGFR mutation were associated with alteration of specific airway genera and metabolic function of sputum microbiota. John Wiley & Sons Australia, Ltd 2022-02-10 2022-03 /pmc/articles/PMC8930493/ /pubmed/35142041 http://dx.doi.org/10.1111/1759-7714.14340 Text en © 2022 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Huang, Dan Hui He, Jing Su, Xiao Fang Wen, Ya Na Zhang, Shu Jia Liu, Lai Yu Zhao, Haijin Ye, Cui Pin Wu, Jian Hua Cai, Shaoxi Dong, Hangming The airway microbiota of non‐small cell lung cancer patients and its relationship to tumor stage and EGFR gene mutation |
title | The airway microbiota of non‐small cell lung cancer patients and its relationship to tumor stage and
EGFR
gene mutation |
title_full | The airway microbiota of non‐small cell lung cancer patients and its relationship to tumor stage and
EGFR
gene mutation |
title_fullStr | The airway microbiota of non‐small cell lung cancer patients and its relationship to tumor stage and
EGFR
gene mutation |
title_full_unstemmed | The airway microbiota of non‐small cell lung cancer patients and its relationship to tumor stage and
EGFR
gene mutation |
title_short | The airway microbiota of non‐small cell lung cancer patients and its relationship to tumor stage and
EGFR
gene mutation |
title_sort | airway microbiota of non‐small cell lung cancer patients and its relationship to tumor stage and
egfr
gene mutation |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930493/ https://www.ncbi.nlm.nih.gov/pubmed/35142041 http://dx.doi.org/10.1111/1759-7714.14340 |
work_keys_str_mv | AT huangdanhui theairwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT hejing theairwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT suxiaofang theairwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT wenyana theairwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT zhangshujia theairwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT liulaiyu theairwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT zhaohaijin theairwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT yecuipin theairwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT wujianhua theairwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT caishaoxi theairwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT donghangming theairwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT huangdanhui airwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT hejing airwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT suxiaofang airwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT wenyana airwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT zhangshujia airwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT liulaiyu airwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT zhaohaijin airwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT yecuipin airwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT wujianhua airwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT caishaoxi airwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation AT donghangming airwaymicrobiotaofnonsmallcelllungcancerpatientsanditsrelationshiptotumorstageandegfrgenemutation |