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Dysbiosis of the Gut Microbiome Is Associated With Histopathology of Lung Cancer

Lung cancer is a malignancy with high incidence and mortality worldwide. Previous studies have shown that the gut microbiome plays an important role in the development and progression of metabolic cancers. However, data on the characteristics of the gut microbiome with different histopathology types...

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Autores principales: Qin, Xiong, Bi, Ling, Yang, Wenxiao, He, Yiyun, Gu, Yifeng, Yang, Yong, Gong, Yabin, Wang, Yichao, Yan, Xiaoxia, Xu, Ling, Xiao, Haibo, Jiao, Lijing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237568/
https://www.ncbi.nlm.nih.gov/pubmed/35774470
http://dx.doi.org/10.3389/fmicb.2022.918823
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author Qin, Xiong
Bi, Ling
Yang, Wenxiao
He, Yiyun
Gu, Yifeng
Yang, Yong
Gong, Yabin
Wang, Yichao
Yan, Xiaoxia
Xu, Ling
Xiao, Haibo
Jiao, Lijing
author_facet Qin, Xiong
Bi, Ling
Yang, Wenxiao
He, Yiyun
Gu, Yifeng
Yang, Yong
Gong, Yabin
Wang, Yichao
Yan, Xiaoxia
Xu, Ling
Xiao, Haibo
Jiao, Lijing
author_sort Qin, Xiong
collection PubMed
description Lung cancer is a malignancy with high incidence and mortality worldwide. Previous studies have shown that the gut microbiome plays an important role in the development and progression of metabolic cancers. However, data on the characteristics of the gut microbiome with different histopathology types of lung cancer remain scant. We collected stool samples from 28 healthy people (HP) and 61 lung cancer patients. The lung cancer patients were classified into three types according to their histopathology: Atypical Adenomatous Hyperplasia/Adenocarcinoma in situ (AAH/AIS), Minimally Invasive Adenocarcinoma (MIA), and Invasive Adenocarcinoma (IA). In addition, we employed 16S rRNA gene amplicon sequencing to analyze the characteristics of the gut microbiome in these patients. Our analysis revealed that the categorized cancer patients had unique intestinal flora characteristics, and had lower density and flora diversity compared to healthy people. Besides, the structure of the flora families and genera was more complex, and each group presented specific pathogenic microbiota. The patients in the AAH/AIS group and HP group had relatively similar flora structure compared with the IA and MIA groups. In addition, we identified several flora markers that showed significant changes with the development of lung cancer. Lung cancer gut microbiota showed a decrease in short-chain fatty acids (SCFAs) producing and anti-inflammatory bacteria compared to healthy people, while some pathogenic bacteria such as proinflammatory or tumor-promoting bacteria were more abundant in lung cancer patients. On the other hand, the Kyoto Encyclopedia of Genes and Genomes (KEGG) and Clusters of Orthologous Group (COG) annotation demonstrated suppression of some dominant metabolism-related pathways in lung cancer. These findings provide new biomarkers for the diagnosis and prognostic assessment of lung cancer and lay the basis for novel targeted therapeutic strategies for the prevention and treatment of lung cancer. CLINICAL TRIAL REGISTRATION: [www.ClinicalTrials.gov], identifier [NCT03244605].
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spelling pubmed-92375682022-06-29 Dysbiosis of the Gut Microbiome Is Associated With Histopathology of Lung Cancer Qin, Xiong Bi, Ling Yang, Wenxiao He, Yiyun Gu, Yifeng Yang, Yong Gong, Yabin Wang, Yichao Yan, Xiaoxia Xu, Ling Xiao, Haibo Jiao, Lijing Front Microbiol Microbiology Lung cancer is a malignancy with high incidence and mortality worldwide. Previous studies have shown that the gut microbiome plays an important role in the development and progression of metabolic cancers. However, data on the characteristics of the gut microbiome with different histopathology types of lung cancer remain scant. We collected stool samples from 28 healthy people (HP) and 61 lung cancer patients. The lung cancer patients were classified into three types according to their histopathology: Atypical Adenomatous Hyperplasia/Adenocarcinoma in situ (AAH/AIS), Minimally Invasive Adenocarcinoma (MIA), and Invasive Adenocarcinoma (IA). In addition, we employed 16S rRNA gene amplicon sequencing to analyze the characteristics of the gut microbiome in these patients. Our analysis revealed that the categorized cancer patients had unique intestinal flora characteristics, and had lower density and flora diversity compared to healthy people. Besides, the structure of the flora families and genera was more complex, and each group presented specific pathogenic microbiota. The patients in the AAH/AIS group and HP group had relatively similar flora structure compared with the IA and MIA groups. In addition, we identified several flora markers that showed significant changes with the development of lung cancer. Lung cancer gut microbiota showed a decrease in short-chain fatty acids (SCFAs) producing and anti-inflammatory bacteria compared to healthy people, while some pathogenic bacteria such as proinflammatory or tumor-promoting bacteria were more abundant in lung cancer patients. On the other hand, the Kyoto Encyclopedia of Genes and Genomes (KEGG) and Clusters of Orthologous Group (COG) annotation demonstrated suppression of some dominant metabolism-related pathways in lung cancer. These findings provide new biomarkers for the diagnosis and prognostic assessment of lung cancer and lay the basis for novel targeted therapeutic strategies for the prevention and treatment of lung cancer. CLINICAL TRIAL REGISTRATION: [www.ClinicalTrials.gov], identifier [NCT03244605]. Frontiers Media S.A. 2022-06-14 /pmc/articles/PMC9237568/ /pubmed/35774470 http://dx.doi.org/10.3389/fmicb.2022.918823 Text en Copyright © 2022 Qin, Bi, Yang, He, Gu, Yang, Gong, Wang, Yan, Xu, Xiao and Jiao. 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 Microbiology
Qin, Xiong
Bi, Ling
Yang, Wenxiao
He, Yiyun
Gu, Yifeng
Yang, Yong
Gong, Yabin
Wang, Yichao
Yan, Xiaoxia
Xu, Ling
Xiao, Haibo
Jiao, Lijing
Dysbiosis of the Gut Microbiome Is Associated With Histopathology of Lung Cancer
title Dysbiosis of the Gut Microbiome Is Associated With Histopathology of Lung Cancer
title_full Dysbiosis of the Gut Microbiome Is Associated With Histopathology of Lung Cancer
title_fullStr Dysbiosis of the Gut Microbiome Is Associated With Histopathology of Lung Cancer
title_full_unstemmed Dysbiosis of the Gut Microbiome Is Associated With Histopathology of Lung Cancer
title_short Dysbiosis of the Gut Microbiome Is Associated With Histopathology of Lung Cancer
title_sort dysbiosis of the gut microbiome is associated with histopathology of lung cancer
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237568/
https://www.ncbi.nlm.nih.gov/pubmed/35774470
http://dx.doi.org/10.3389/fmicb.2022.918823
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