Cargando…
Comparative Analysis of Age- and Gender-Associated Microbiome in Lung Adenocarcinoma and Lung Squamous Cell Carcinoma
The intra-tumor microbiota has been increasingly implicated in cancer pathogenesis. In this study, we aimed to examine the microbiome in lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC) and determine its compositional differences with relation to age and gender. After grouping 497...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352186/ https://www.ncbi.nlm.nih.gov/pubmed/32498338 http://dx.doi.org/10.3390/cancers12061447 |
_version_ | 1783557578842701824 |
---|---|
author | Wong, Lindsay M. Shende, Neil Li, Wei Tse Castaneda, Grant Apostol, Lauren Chang, Eric Y. Ongkeko, Weg M. |
author_facet | Wong, Lindsay M. Shende, Neil Li, Wei Tse Castaneda, Grant Apostol, Lauren Chang, Eric Y. Ongkeko, Weg M. |
author_sort | Wong, Lindsay M. |
collection | PubMed |
description | The intra-tumor microbiota has been increasingly implicated in cancer pathogenesis. In this study, we aimed to examine the microbiome in lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC) and determine its compositional differences with relation to age and gender. After grouping 497 LUAD and 433 LUSC patients by age and gender and removing potential contaminants, we identified differentially abundant microbes in each patient cohort vs. adjacent normal samples. We then correlated dysregulated microbes with patient survival rates, immune infiltration, immune and cancer pathways, and genomic alterations. We found that most age and gender cohorts in both LUAD and LUSC contained unique, significantly dysregulated microbes. For example, LUAD-associated Escherichia coli str. K-12 substr. W3110 was dysregulated in older female and male patients and correlated with both patient survival and genomic alterations. For LUSC, the most prominent bacterial species that we identified was Pseudomonas putida str. KT2440, which was uniquely associated with young LUSC male patients and immune infiltration. In conclusion, we found differentially abundant microbes implicated with age and gender that are also associated with genomic alterations and immune dysregulations. Further investigation should be conducted to determine the relationship between gender and age-associated microbes and the pathogenesis of lung cancer. |
format | Online Article Text |
id | pubmed-7352186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73521862020-07-15 Comparative Analysis of Age- and Gender-Associated Microbiome in Lung Adenocarcinoma and Lung Squamous Cell Carcinoma Wong, Lindsay M. Shende, Neil Li, Wei Tse Castaneda, Grant Apostol, Lauren Chang, Eric Y. Ongkeko, Weg M. Cancers (Basel) Article The intra-tumor microbiota has been increasingly implicated in cancer pathogenesis. In this study, we aimed to examine the microbiome in lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC) and determine its compositional differences with relation to age and gender. After grouping 497 LUAD and 433 LUSC patients by age and gender and removing potential contaminants, we identified differentially abundant microbes in each patient cohort vs. adjacent normal samples. We then correlated dysregulated microbes with patient survival rates, immune infiltration, immune and cancer pathways, and genomic alterations. We found that most age and gender cohorts in both LUAD and LUSC contained unique, significantly dysregulated microbes. For example, LUAD-associated Escherichia coli str. K-12 substr. W3110 was dysregulated in older female and male patients and correlated with both patient survival and genomic alterations. For LUSC, the most prominent bacterial species that we identified was Pseudomonas putida str. KT2440, which was uniquely associated with young LUSC male patients and immune infiltration. In conclusion, we found differentially abundant microbes implicated with age and gender that are also associated with genomic alterations and immune dysregulations. Further investigation should be conducted to determine the relationship between gender and age-associated microbes and the pathogenesis of lung cancer. MDPI 2020-06-02 /pmc/articles/PMC7352186/ /pubmed/32498338 http://dx.doi.org/10.3390/cancers12061447 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wong, Lindsay M. Shende, Neil Li, Wei Tse Castaneda, Grant Apostol, Lauren Chang, Eric Y. Ongkeko, Weg M. Comparative Analysis of Age- and Gender-Associated Microbiome in Lung Adenocarcinoma and Lung Squamous Cell Carcinoma |
title | Comparative Analysis of Age- and Gender-Associated Microbiome in Lung Adenocarcinoma and Lung Squamous Cell Carcinoma |
title_full | Comparative Analysis of Age- and Gender-Associated Microbiome in Lung Adenocarcinoma and Lung Squamous Cell Carcinoma |
title_fullStr | Comparative Analysis of Age- and Gender-Associated Microbiome in Lung Adenocarcinoma and Lung Squamous Cell Carcinoma |
title_full_unstemmed | Comparative Analysis of Age- and Gender-Associated Microbiome in Lung Adenocarcinoma and Lung Squamous Cell Carcinoma |
title_short | Comparative Analysis of Age- and Gender-Associated Microbiome in Lung Adenocarcinoma and Lung Squamous Cell Carcinoma |
title_sort | comparative analysis of age- and gender-associated microbiome in lung adenocarcinoma and lung squamous cell carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352186/ https://www.ncbi.nlm.nih.gov/pubmed/32498338 http://dx.doi.org/10.3390/cancers12061447 |
work_keys_str_mv | AT wonglindsaym comparativeanalysisofageandgenderassociatedmicrobiomeinlungadenocarcinomaandlungsquamouscellcarcinoma AT shendeneil comparativeanalysisofageandgenderassociatedmicrobiomeinlungadenocarcinomaandlungsquamouscellcarcinoma AT liweitse comparativeanalysisofageandgenderassociatedmicrobiomeinlungadenocarcinomaandlungsquamouscellcarcinoma AT castanedagrant comparativeanalysisofageandgenderassociatedmicrobiomeinlungadenocarcinomaandlungsquamouscellcarcinoma AT apostollauren comparativeanalysisofageandgenderassociatedmicrobiomeinlungadenocarcinomaandlungsquamouscellcarcinoma AT changericy comparativeanalysisofageandgenderassociatedmicrobiomeinlungadenocarcinomaandlungsquamouscellcarcinoma AT ongkekowegm comparativeanalysisofageandgenderassociatedmicrobiomeinlungadenocarcinomaandlungsquamouscellcarcinoma |