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Gut Microbiota Dysbiosis in the Development and Progression of Gastric Cancer
OBJECTIVES: This study aims to explore gut microbiota dysbiosis in the histological stages of gastric cancer (GC). METHODS: Feces samples and clinical characteristics were collected from patients with different stages of GC, including 15 superficial gastritis (SG), 13 atrophic gastritis (AG), 8 gast...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441395/ https://www.ncbi.nlm.nih.gov/pubmed/36072968 http://dx.doi.org/10.1155/2022/9971619 |
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author | Miao, Yingying Tang, Hui Zhai, Qizhi Liu, Lu Xia, Lu Wu, Wenhan Xu, Yue Wang, Jianning |
author_facet | Miao, Yingying Tang, Hui Zhai, Qizhi Liu, Lu Xia, Lu Wu, Wenhan Xu, Yue Wang, Jianning |
author_sort | Miao, Yingying |
collection | PubMed |
description | OBJECTIVES: This study aims to explore gut microbiota dysbiosis in the histological stages of gastric cancer (GC). METHODS: Feces samples and clinical characteristics were collected from patients with different stages of GC, including 15 superficial gastritis (SG), 13 atrophic gastritis (AG), 8 gastric mucosal atypical hyperplasia (GMAH), and 15 advanced GC cases. The diversity and composition of gut microbiota among the four groups were determined by sequencing the V4 region of bacterial 16S rRNA genes. RESULTS: Reduced gut microbial alpha diversity and altered dissimilarity of the microbial community structure were found among the four groups. In addition, 18 species, 6 species, 6 species, and 16 species of bacteria were enriched in the SG, AG, GMAH, and GC groups, respectively, using the linear discriminant analysis (LDA) effect size (LEfSe) analyses. Besides, we found that two new genera, Scardovia and Halomonas, are associated with GC and the metabolic pathways of Genetic information processing and Circulatory System were more abundant in the GC group compared with noncancer groups. CONCLUSIONS: We identified differences in microbial compositional changes across stages of GC. Six genera and two metabolic pathways were more abundant in the GC group than noncancer groups, suggesting that these findings may contribute to the therapy strategies in GC in the near feature. |
format | Online Article Text |
id | pubmed-9441395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-94413952022-09-06 Gut Microbiota Dysbiosis in the Development and Progression of Gastric Cancer Miao, Yingying Tang, Hui Zhai, Qizhi Liu, Lu Xia, Lu Wu, Wenhan Xu, Yue Wang, Jianning J Oncol Research Article OBJECTIVES: This study aims to explore gut microbiota dysbiosis in the histological stages of gastric cancer (GC). METHODS: Feces samples and clinical characteristics were collected from patients with different stages of GC, including 15 superficial gastritis (SG), 13 atrophic gastritis (AG), 8 gastric mucosal atypical hyperplasia (GMAH), and 15 advanced GC cases. The diversity and composition of gut microbiota among the four groups were determined by sequencing the V4 region of bacterial 16S rRNA genes. RESULTS: Reduced gut microbial alpha diversity and altered dissimilarity of the microbial community structure were found among the four groups. In addition, 18 species, 6 species, 6 species, and 16 species of bacteria were enriched in the SG, AG, GMAH, and GC groups, respectively, using the linear discriminant analysis (LDA) effect size (LEfSe) analyses. Besides, we found that two new genera, Scardovia and Halomonas, are associated with GC and the metabolic pathways of Genetic information processing and Circulatory System were more abundant in the GC group compared with noncancer groups. CONCLUSIONS: We identified differences in microbial compositional changes across stages of GC. Six genera and two metabolic pathways were more abundant in the GC group than noncancer groups, suggesting that these findings may contribute to the therapy strategies in GC in the near feature. Hindawi 2022-08-28 /pmc/articles/PMC9441395/ /pubmed/36072968 http://dx.doi.org/10.1155/2022/9971619 Text en Copyright © 2022 Yingying Miao et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Miao, Yingying Tang, Hui Zhai, Qizhi Liu, Lu Xia, Lu Wu, Wenhan Xu, Yue Wang, Jianning Gut Microbiota Dysbiosis in the Development and Progression of Gastric Cancer |
title | Gut Microbiota Dysbiosis in the Development and Progression of Gastric Cancer |
title_full | Gut Microbiota Dysbiosis in the Development and Progression of Gastric Cancer |
title_fullStr | Gut Microbiota Dysbiosis in the Development and Progression of Gastric Cancer |
title_full_unstemmed | Gut Microbiota Dysbiosis in the Development and Progression of Gastric Cancer |
title_short | Gut Microbiota Dysbiosis in the Development and Progression of Gastric Cancer |
title_sort | gut microbiota dysbiosis in the development and progression of gastric cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441395/ https://www.ncbi.nlm.nih.gov/pubmed/36072968 http://dx.doi.org/10.1155/2022/9971619 |
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