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Microbiota and metabolites alterations in proximal and distal gastric cancer patients

BACKGROUND: Globally, gastric cancer is the third most common cancer and the third leading cause of cancer death. Proximal and distal gastric cancers have distinct clinical and biological behaviors. The microbial composition and metabolic differences in proximal and distal gastric cancers have not b...

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Autores principales: Yang, Yan, Dai, Daofeng, Jin, Wen, Huang, Yingying, Zhang, Yingzi, Chen, Yiran, Wang, Wankun, Lin, Wu, Chen, Xiangliu, Zhang, Jing, Wang, Haohao, Zhang, Haibin, Teng, Lisong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524040/
https://www.ncbi.nlm.nih.gov/pubmed/36180919
http://dx.doi.org/10.1186/s12967-022-03650-x
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author Yang, Yan
Dai, Daofeng
Jin, Wen
Huang, Yingying
Zhang, Yingzi
Chen, Yiran
Wang, Wankun
Lin, Wu
Chen, Xiangliu
Zhang, Jing
Wang, Haohao
Zhang, Haibin
Teng, Lisong
author_facet Yang, Yan
Dai, Daofeng
Jin, Wen
Huang, Yingying
Zhang, Yingzi
Chen, Yiran
Wang, Wankun
Lin, Wu
Chen, Xiangliu
Zhang, Jing
Wang, Haohao
Zhang, Haibin
Teng, Lisong
author_sort Yang, Yan
collection PubMed
description BACKGROUND: Globally, gastric cancer is the third most common cancer and the third leading cause of cancer death. Proximal and distal gastric cancers have distinct clinical and biological behaviors. The microbial composition and metabolic differences in proximal and distal gastric cancers have not been fully studied and discussed. METHODS: In this study, the gastric microbiome of 13 proximal gastric cancer tissues, 16 distal gastric cancer tissues, and their matched non-tumor tissues were characterized using 16S rRNA amplicon sequencing. Additionally, 10 proximal gastric cancer tissues, 11 distal gastric cancer tissues, and their matched non-tumor tissues were assessed by untargeted metabolomics. RESULTS: There was no significant difference in microbial diversity and richness between the proximal and distal gastric cancer tissues. At the genus level, the abundance of Rikenellaceae_RC9_gut_group, Porphyromonas, Catonella, Proteus, Oribacterium, and Moraxella were significantly increased in Proximal T, whereas that of Methylobacterium_Methylorubrum was significantly increased in Distal T. The untargeted metabolomics analysis revealed 30 discriminative metabolites between Distal T and Distal N. In contrast, there were only 4 discriminative metabolites between Proximal T and Proximal N. In distal gastric cancer, different metabolites were scattered through multiple pathway, including the sphingolipid signaling pathway, arginine biosynthesis, protein digestion and absorption, alanine, aspartate and, glutamate metabolism, etc.In proximal gastric cancer, differential microbial metabolites were mainly related to hormone metabolism. CONCLUSION: Methylobacterium-Methylorubrum was significantly increased in Distal T, positively correlated with cancer-promoting metabolites, and negatively correlated with cancer-inhibiting metabolites. Rikenellaceae_RC_gut_group was significantly increased in Proximal T and positively correlated with cancer-promoting metabolites. Further studies regarding the functions of the above-mentioned microorganisms and metabolites were warranted as the results may reveal the different mechanisms underlying the occurrence and development of proximal and distal gastric cancers and provide a basis for future treatments. IMPORTANCE: First, the differences in microbial composition and metabolites between the proximal and distal gastric cancers were described; then, the correlation between microbiota and metabolites was preliminarily discussed. These microbes and metabolites deserve further investigations as they may reveal the different mechanisms involved in the occurrence and development of proximal and distal gastric cancers and provide a basis for future treatments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-022-03650-x.
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spelling pubmed-95240402022-10-01 Microbiota and metabolites alterations in proximal and distal gastric cancer patients Yang, Yan Dai, Daofeng Jin, Wen Huang, Yingying Zhang, Yingzi Chen, Yiran Wang, Wankun Lin, Wu Chen, Xiangliu Zhang, Jing Wang, Haohao Zhang, Haibin Teng, Lisong J Transl Med Research BACKGROUND: Globally, gastric cancer is the third most common cancer and the third leading cause of cancer death. Proximal and distal gastric cancers have distinct clinical and biological behaviors. The microbial composition and metabolic differences in proximal and distal gastric cancers have not been fully studied and discussed. METHODS: In this study, the gastric microbiome of 13 proximal gastric cancer tissues, 16 distal gastric cancer tissues, and their matched non-tumor tissues were characterized using 16S rRNA amplicon sequencing. Additionally, 10 proximal gastric cancer tissues, 11 distal gastric cancer tissues, and their matched non-tumor tissues were assessed by untargeted metabolomics. RESULTS: There was no significant difference in microbial diversity and richness between the proximal and distal gastric cancer tissues. At the genus level, the abundance of Rikenellaceae_RC9_gut_group, Porphyromonas, Catonella, Proteus, Oribacterium, and Moraxella were significantly increased in Proximal T, whereas that of Methylobacterium_Methylorubrum was significantly increased in Distal T. The untargeted metabolomics analysis revealed 30 discriminative metabolites between Distal T and Distal N. In contrast, there were only 4 discriminative metabolites between Proximal T and Proximal N. In distal gastric cancer, different metabolites were scattered through multiple pathway, including the sphingolipid signaling pathway, arginine biosynthesis, protein digestion and absorption, alanine, aspartate and, glutamate metabolism, etc.In proximal gastric cancer, differential microbial metabolites were mainly related to hormone metabolism. CONCLUSION: Methylobacterium-Methylorubrum was significantly increased in Distal T, positively correlated with cancer-promoting metabolites, and negatively correlated with cancer-inhibiting metabolites. Rikenellaceae_RC_gut_group was significantly increased in Proximal T and positively correlated with cancer-promoting metabolites. Further studies regarding the functions of the above-mentioned microorganisms and metabolites were warranted as the results may reveal the different mechanisms underlying the occurrence and development of proximal and distal gastric cancers and provide a basis for future treatments. IMPORTANCE: First, the differences in microbial composition and metabolites between the proximal and distal gastric cancers were described; then, the correlation between microbiota and metabolites was preliminarily discussed. These microbes and metabolites deserve further investigations as they may reveal the different mechanisms involved in the occurrence and development of proximal and distal gastric cancers and provide a basis for future treatments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-022-03650-x. BioMed Central 2022-09-30 /pmc/articles/PMC9524040/ /pubmed/36180919 http://dx.doi.org/10.1186/s12967-022-03650-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yang, Yan
Dai, Daofeng
Jin, Wen
Huang, Yingying
Zhang, Yingzi
Chen, Yiran
Wang, Wankun
Lin, Wu
Chen, Xiangliu
Zhang, Jing
Wang, Haohao
Zhang, Haibin
Teng, Lisong
Microbiota and metabolites alterations in proximal and distal gastric cancer patients
title Microbiota and metabolites alterations in proximal and distal gastric cancer patients
title_full Microbiota and metabolites alterations in proximal and distal gastric cancer patients
title_fullStr Microbiota and metabolites alterations in proximal and distal gastric cancer patients
title_full_unstemmed Microbiota and metabolites alterations in proximal and distal gastric cancer patients
title_short Microbiota and metabolites alterations in proximal and distal gastric cancer patients
title_sort microbiota and metabolites alterations in proximal and distal gastric cancer patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524040/
https://www.ncbi.nlm.nih.gov/pubmed/36180919
http://dx.doi.org/10.1186/s12967-022-03650-x
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