Metabolite quantification of faecal extracts from colorectal cancer patients and healthy controls

Le Gall, Gwénaëlle, Guttula, Kiran, Kellingray, Lee, Tett, Adrian J, ten Hoopen, Rogier, Kemsley, Kate E, Savva, George M, Ibrahim, Ashraf and Narbad, Arjan (2018) Metabolite quantification of faecal extracts from colorectal cancer patients and healthy controls. Oncotarget, 9 (70). pp. 33278-33289. ISSN 1949-2553

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Abstract

Colorectal cancer (CRC), a primary cause of morbidity and mortality worldwide is expected to rise in the coming years. A better understanding of the metabolic changes taking place during the disease progression is needed for effective improvements of screening strategies and treatments. In the present study, Nuclear Magnetic Resonance (NMR) metabolomics was used to quantify the absolute concentrations of metabolites in faecal extracts from two cohorts of CRC patients and healthy controls. The quantification of over 80 compounds revealed that patients with CRC had increased faecal concentrations of branched chain fatty acids (BCFA), isovalerate and isobutyrate plus valerate and phenylacetate but diminished concentrations of amino acids, sugars, methanol and bile acids (deoxycholate, lithodeoxycholate and cholate). These results suggest that alterations in microbial activity and composition could have triggered an increase in utilisation of host intestinal slough cells and mucins and led to an increase in BCFA, valerate and phenylacetate. Concurrently, a general reduction in the microbial metabolic function may have led to reduced levels of other components (amino acids, sugars and bile acids) normally produced under healthy conditions. This study provides a thorough listing of the most abundant compounds found in human faecal waters and presents a template for absolute quantification of metabolites. The production of BCFA and phenylacetate in colonic carcinogenesis warrants further investigations.

Item Type: Article
Depositing User: LivePure Connector
Date Deposited: 26 Oct 2018 16:31
Last Modified: 22 Jul 2020 02:38
URI: https://ueaeprints.uea.ac.uk/id/eprint/68680
DOI: 10.18632/oncotarget.26022

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