Interactions between gastric microbiota and metabolites in gastric cancer
Abstract The development and progression of gastric cancer (GC) is greatly influenced by gastric microbiota and their metabolites. Here, we characterized the gastric microbiome and metabolome profiles of 37 GC tumor tissues and matched non-tumor tissues using 16s rRNA gene sequencing and ultrahigh p...
Guardado en:
Autores principales: | , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Publishing Group
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/b2e1d0b747d24b8a9d0e8536082b18cd |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:b2e1d0b747d24b8a9d0e8536082b18cd |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:b2e1d0b747d24b8a9d0e8536082b18cd2021-11-28T12:04:27ZInteractions between gastric microbiota and metabolites in gastric cancer10.1038/s41419-021-04396-y2041-4889https://doaj.org/article/b2e1d0b747d24b8a9d0e8536082b18cd2021-11-01T00:00:00Zhttps://doi.org/10.1038/s41419-021-04396-yhttps://doaj.org/toc/2041-4889Abstract The development and progression of gastric cancer (GC) is greatly influenced by gastric microbiota and their metabolites. Here, we characterized the gastric microbiome and metabolome profiles of 37 GC tumor tissues and matched non-tumor tissues using 16s rRNA gene sequencing and ultrahigh performance liquid chromatography tandem mass spectrometry, respectively. Microbial diversity and richness were higher in GC tumor tissues than in non-tumor tissues. The abundance of Helicobacter was increased in non-tumor tissues, while the abundance of Lactobacillus, Streptococcus, Bacteroides, Prevotella, and 6 additional genera was increased in the tumor tissues. The untargeted metabolome analysis revealed 150 discriminative metabolites, among which the relative abundance of the amino acids, carbohydrates and carbohydrate conjugates, glycerophospholipids, and nucleosides was higher in tumor tissues compared to non-tumor tissues. The targeted metabolome analysis further demonstrated that the combination of 1-methylnicotinamide and N-acetyl-D-glucosamine-6-phosphate could serve as a robust biomarker for distinction between GC tumors and non-tumor tissues. Correlation analysis revealed that Helicobacter and Lactobacillus were negatively and positively correlated with the majority of differential metabolites in the classes of amino acids, carbohydrates, nucleosides, nucleotides, and glycerophospholipids, respectively, suggesting that Helicobacter and Lactobacillus might play a role in degradation and synthesis of the majority of differential metabolites in these classes, respectively. Acinetobacter, Comamonas, Faecalibacterium, Sphingomonas, and Streptococcus were also significantly correlated with many differential amino acids, carbohydrates, nucleosides, nucleotides, and glycerophospholipids. In conclusion, the differences in metabolome profiles between GC tumor and matched non-tumor tissues may be partly due to the collective activities of Helicobacter, Lactobacillus, and other bacteria, which eventually affects GC carcinogenesis and progression.Daofeng DaiYan YangJieqing YuTianfeng DangWenjing QinLisong TengJing YeHongqun JiangNature Publishing GrouparticleCytologyQH573-671ENCell Death and Disease, Vol 12, Iss 12, Pp 1-11 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Cytology QH573-671 |
spellingShingle |
Cytology QH573-671 Daofeng Dai Yan Yang Jieqing Yu Tianfeng Dang Wenjing Qin Lisong Teng Jing Ye Hongqun Jiang Interactions between gastric microbiota and metabolites in gastric cancer |
description |
Abstract The development and progression of gastric cancer (GC) is greatly influenced by gastric microbiota and their metabolites. Here, we characterized the gastric microbiome and metabolome profiles of 37 GC tumor tissues and matched non-tumor tissues using 16s rRNA gene sequencing and ultrahigh performance liquid chromatography tandem mass spectrometry, respectively. Microbial diversity and richness were higher in GC tumor tissues than in non-tumor tissues. The abundance of Helicobacter was increased in non-tumor tissues, while the abundance of Lactobacillus, Streptococcus, Bacteroides, Prevotella, and 6 additional genera was increased in the tumor tissues. The untargeted metabolome analysis revealed 150 discriminative metabolites, among which the relative abundance of the amino acids, carbohydrates and carbohydrate conjugates, glycerophospholipids, and nucleosides was higher in tumor tissues compared to non-tumor tissues. The targeted metabolome analysis further demonstrated that the combination of 1-methylnicotinamide and N-acetyl-D-glucosamine-6-phosphate could serve as a robust biomarker for distinction between GC tumors and non-tumor tissues. Correlation analysis revealed that Helicobacter and Lactobacillus were negatively and positively correlated with the majority of differential metabolites in the classes of amino acids, carbohydrates, nucleosides, nucleotides, and glycerophospholipids, respectively, suggesting that Helicobacter and Lactobacillus might play a role in degradation and synthesis of the majority of differential metabolites in these classes, respectively. Acinetobacter, Comamonas, Faecalibacterium, Sphingomonas, and Streptococcus were also significantly correlated with many differential amino acids, carbohydrates, nucleosides, nucleotides, and glycerophospholipids. In conclusion, the differences in metabolome profiles between GC tumor and matched non-tumor tissues may be partly due to the collective activities of Helicobacter, Lactobacillus, and other bacteria, which eventually affects GC carcinogenesis and progression. |
format |
article |
author |
Daofeng Dai Yan Yang Jieqing Yu Tianfeng Dang Wenjing Qin Lisong Teng Jing Ye Hongqun Jiang |
author_facet |
Daofeng Dai Yan Yang Jieqing Yu Tianfeng Dang Wenjing Qin Lisong Teng Jing Ye Hongqun Jiang |
author_sort |
Daofeng Dai |
title |
Interactions between gastric microbiota and metabolites in gastric cancer |
title_short |
Interactions between gastric microbiota and metabolites in gastric cancer |
title_full |
Interactions between gastric microbiota and metabolites in gastric cancer |
title_fullStr |
Interactions between gastric microbiota and metabolites in gastric cancer |
title_full_unstemmed |
Interactions between gastric microbiota and metabolites in gastric cancer |
title_sort |
interactions between gastric microbiota and metabolites in gastric cancer |
publisher |
Nature Publishing Group |
publishDate |
2021 |
url |
https://doaj.org/article/b2e1d0b747d24b8a9d0e8536082b18cd |
work_keys_str_mv |
AT daofengdai interactionsbetweengastricmicrobiotaandmetabolitesingastriccancer AT yanyang interactionsbetweengastricmicrobiotaandmetabolitesingastriccancer AT jieqingyu interactionsbetweengastricmicrobiotaandmetabolitesingastriccancer AT tianfengdang interactionsbetweengastricmicrobiotaandmetabolitesingastriccancer AT wenjingqin interactionsbetweengastricmicrobiotaandmetabolitesingastriccancer AT lisongteng interactionsbetweengastricmicrobiotaandmetabolitesingastriccancer AT jingye interactionsbetweengastricmicrobiotaandmetabolitesingastriccancer AT hongqunjiang interactionsbetweengastricmicrobiotaandmetabolitesingastriccancer |
_version_ |
1718408220553248768 |