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Causal relationship between gut microbiota and cancers: a two-sample Mendelian randomisation study

BACKGROUND: Evidence from observational studies and clinical trials suggests that the gut microbiota is associated with cancer. However, the causal association between gut microbiota and cancer remains to be determined. METHODS: We first identified two sets of gut microbiota based on phylum, class,...

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Autores principales: Long, Yiwen, Tang, Lanhua, Zhou, Yangying, Zhao, Shushan, Zhu, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945666/
https://www.ncbi.nlm.nih.gov/pubmed/36810112
http://dx.doi.org/10.1186/s12916-023-02761-6
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author Long, Yiwen
Tang, Lanhua
Zhou, Yangying
Zhao, Shushan
Zhu, Hong
author_facet Long, Yiwen
Tang, Lanhua
Zhou, Yangying
Zhao, Shushan
Zhu, Hong
author_sort Long, Yiwen
collection PubMed
description BACKGROUND: Evidence from observational studies and clinical trials suggests that the gut microbiota is associated with cancer. However, the causal association between gut microbiota and cancer remains to be determined. METHODS: We first identified two sets of gut microbiota based on phylum, class, order, family, and genus level information, and cancer data were obtained from the IEU Open GWAS project. We then performed two-sample Mendelian randomisation (MR) to determine whether the gut microbiota is causally associated with eight cancer types. Furthermore, we performed a bi-directional MR analysis to examine the direction of the causal relations. RESULTS: We identified 11 causal relationships between genetic liability in the gut microbiome and cancer, including those involving the genus Bifidobacterium. We found 17 strong associations between genetic liability in the gut microbiome and cancer. Moreover, we found 24 associations between genetic liability in the gut microbiome and cancer using multiple datasets. CONCLUSIONS: Our MR analysis revealed that the gut microbiota was causally associated with cancers and may be useful in providing new insights for further mechanistic and clinical studies of microbiota-mediated cancer. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-023-02761-6.
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spelling pubmed-99456662023-02-23 Causal relationship between gut microbiota and cancers: a two-sample Mendelian randomisation study Long, Yiwen Tang, Lanhua Zhou, Yangying Zhao, Shushan Zhu, Hong BMC Med Research Article BACKGROUND: Evidence from observational studies and clinical trials suggests that the gut microbiota is associated with cancer. However, the causal association between gut microbiota and cancer remains to be determined. METHODS: We first identified two sets of gut microbiota based on phylum, class, order, family, and genus level information, and cancer data were obtained from the IEU Open GWAS project. We then performed two-sample Mendelian randomisation (MR) to determine whether the gut microbiota is causally associated with eight cancer types. Furthermore, we performed a bi-directional MR analysis to examine the direction of the causal relations. RESULTS: We identified 11 causal relationships between genetic liability in the gut microbiome and cancer, including those involving the genus Bifidobacterium. We found 17 strong associations between genetic liability in the gut microbiome and cancer. Moreover, we found 24 associations between genetic liability in the gut microbiome and cancer using multiple datasets. CONCLUSIONS: Our MR analysis revealed that the gut microbiota was causally associated with cancers and may be useful in providing new insights for further mechanistic and clinical studies of microbiota-mediated cancer. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-023-02761-6. BioMed Central 2023-02-21 /pmc/articles/PMC9945666/ /pubmed/36810112 http://dx.doi.org/10.1186/s12916-023-02761-6 Text en © The Author(s) 2023 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 Article
Long, Yiwen
Tang, Lanhua
Zhou, Yangying
Zhao, Shushan
Zhu, Hong
Causal relationship between gut microbiota and cancers: a two-sample Mendelian randomisation study
title Causal relationship between gut microbiota and cancers: a two-sample Mendelian randomisation study
title_full Causal relationship between gut microbiota and cancers: a two-sample Mendelian randomisation study
title_fullStr Causal relationship between gut microbiota and cancers: a two-sample Mendelian randomisation study
title_full_unstemmed Causal relationship between gut microbiota and cancers: a two-sample Mendelian randomisation study
title_short Causal relationship between gut microbiota and cancers: a two-sample Mendelian randomisation study
title_sort causal relationship between gut microbiota and cancers: a two-sample mendelian randomisation study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945666/
https://www.ncbi.nlm.nih.gov/pubmed/36810112
http://dx.doi.org/10.1186/s12916-023-02761-6
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