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Systematic Review: Contribution of the Gut Microbiome to the Volatile Metabolic Fingerprint of Colorectal Neoplasia

Colorectal cancer (CRC) has been associated with changes in volatile metabolic profiles in several human biological matrices. This enables its non-invasive detection, but the origin of these volatile organic compounds (VOCs) and their relation to the gut microbiome are not yet fully understood. This...

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Autores principales: van Vorstenbosch, Robert, Cheng, Hao Ran, Jonkers, Daisy, Penders, John, Schoon, Erik, Masclee, Ad, van Schooten, Frederik-Jan, Smolinska, Agnieszka, Mujagic, Zlatan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9865897/
https://www.ncbi.nlm.nih.gov/pubmed/36676980
http://dx.doi.org/10.3390/metabo13010055
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author van Vorstenbosch, Robert
Cheng, Hao Ran
Jonkers, Daisy
Penders, John
Schoon, Erik
Masclee, Ad
van Schooten, Frederik-Jan
Smolinska, Agnieszka
Mujagic, Zlatan
author_facet van Vorstenbosch, Robert
Cheng, Hao Ran
Jonkers, Daisy
Penders, John
Schoon, Erik
Masclee, Ad
van Schooten, Frederik-Jan
Smolinska, Agnieszka
Mujagic, Zlatan
author_sort van Vorstenbosch, Robert
collection PubMed
description Colorectal cancer (CRC) has been associated with changes in volatile metabolic profiles in several human biological matrices. This enables its non-invasive detection, but the origin of these volatile organic compounds (VOCs) and their relation to the gut microbiome are not yet fully understood. This systematic review provides an overview of the current understanding of this topic. A systematic search using PubMed, Embase, Medline, Cochrane Library, and the Web of Science according to PRISMA guidelines resulted in seventy-one included studies. In addition, a systematic search was conducted that identified five systematic reviews from which CRC-associated gut microbiota data were extracted. The included studies analyzed VOCs in feces, urine, breath, blood, tissue, and saliva. Eight studies performed microbiota analysis in addition to VOC analysis. The most frequently reported dysregulations over all matrices included short-chain fatty acids, amino acids, proteolytic fermentation products, and products related to the tricarboxylic acid cycle and Warburg metabolism. Many of these dysregulations could be related to the shifts in CRC-associated microbiota, and thus the gut microbiota presumably contributes to the metabolic fingerprint of VOC in CRC. Future research involving VOCs analysis should include simultaneous gut microbiota analysis.
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spelling pubmed-98658972023-01-22 Systematic Review: Contribution of the Gut Microbiome to the Volatile Metabolic Fingerprint of Colorectal Neoplasia van Vorstenbosch, Robert Cheng, Hao Ran Jonkers, Daisy Penders, John Schoon, Erik Masclee, Ad van Schooten, Frederik-Jan Smolinska, Agnieszka Mujagic, Zlatan Metabolites Systematic Review Colorectal cancer (CRC) has been associated with changes in volatile metabolic profiles in several human biological matrices. This enables its non-invasive detection, but the origin of these volatile organic compounds (VOCs) and their relation to the gut microbiome are not yet fully understood. This systematic review provides an overview of the current understanding of this topic. A systematic search using PubMed, Embase, Medline, Cochrane Library, and the Web of Science according to PRISMA guidelines resulted in seventy-one included studies. In addition, a systematic search was conducted that identified five systematic reviews from which CRC-associated gut microbiota data were extracted. The included studies analyzed VOCs in feces, urine, breath, blood, tissue, and saliva. Eight studies performed microbiota analysis in addition to VOC analysis. The most frequently reported dysregulations over all matrices included short-chain fatty acids, amino acids, proteolytic fermentation products, and products related to the tricarboxylic acid cycle and Warburg metabolism. Many of these dysregulations could be related to the shifts in CRC-associated microbiota, and thus the gut microbiota presumably contributes to the metabolic fingerprint of VOC in CRC. Future research involving VOCs analysis should include simultaneous gut microbiota analysis. MDPI 2022-12-30 /pmc/articles/PMC9865897/ /pubmed/36676980 http://dx.doi.org/10.3390/metabo13010055 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Systematic Review
van Vorstenbosch, Robert
Cheng, Hao Ran
Jonkers, Daisy
Penders, John
Schoon, Erik
Masclee, Ad
van Schooten, Frederik-Jan
Smolinska, Agnieszka
Mujagic, Zlatan
Systematic Review: Contribution of the Gut Microbiome to the Volatile Metabolic Fingerprint of Colorectal Neoplasia
title Systematic Review: Contribution of the Gut Microbiome to the Volatile Metabolic Fingerprint of Colorectal Neoplasia
title_full Systematic Review: Contribution of the Gut Microbiome to the Volatile Metabolic Fingerprint of Colorectal Neoplasia
title_fullStr Systematic Review: Contribution of the Gut Microbiome to the Volatile Metabolic Fingerprint of Colorectal Neoplasia
title_full_unstemmed Systematic Review: Contribution of the Gut Microbiome to the Volatile Metabolic Fingerprint of Colorectal Neoplasia
title_short Systematic Review: Contribution of the Gut Microbiome to the Volatile Metabolic Fingerprint of Colorectal Neoplasia
title_sort systematic review: contribution of the gut microbiome to the volatile metabolic fingerprint of colorectal neoplasia
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9865897/
https://www.ncbi.nlm.nih.gov/pubmed/36676980
http://dx.doi.org/10.3390/metabo13010055
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