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Exposure to Microcystin-LR Promotes Colorectal Cancer Progression by Altering Gut Microbiota and Associated Metabolites in APC min/+ Mice.

Authors :
Song Y
Wang X
Lu X
Wang T
Source :
Toxins [Toxins (Basel)] 2024 Apr 30; Vol. 16 (5). Date of Electronic Publication: 2024 Apr 30.
Publication Year :
2024

Abstract

Microcystins (MCs), toxins generated by cyanobacteria, feature microcystin-LR (MC-LR) as one of the most prevalent and toxic variants in aquatic environments. MC-LR not only causes environmental problems but also presents a substantial risk to human health. This study aimed to investigate the impact of MC-LR on APC <superscript>min/+</superscript> mice, considered as an ideal animal model for intestinal tumors. We administered 40 µg/kg MC-LR to mice by gavage for 8 weeks, followed by histopathological examination, microbial diversity and metabolomics analysis. The mice exposed to MC-LR exhibited a significant promotion in colorectal cancer progression and impaired intestinal barrier function in the APC <superscript>min/+</superscript> mice compared with the control. Gut microbial dysbiosis was observed in the MC-LR-exposed mice, manifesting a notable alteration in the structure of the gut microbiota. This included the enrichment of Marvinbryantia , Gordonibacter and Family_XIII_AD3011_group and reductions in Faecalibaculum and Lachnoclostridium . Metabolomics analysis revealed increased bile acid (BA) metabolites in the intestinal contents of the mice exposed to MC-LR, particularly taurocholic acid (TCA), alpha-muricholic acid (α-MCA), 3-dehydrocholic acid (3-DHCA), 7-ketodeoxycholic acid (7-KDCA) and 12-ketodeoxycholic acid (12-KDCA). Moreover, we found that Marvinbryantia and Family_XIII_AD3011_group showed the strongest positive correlation with taurocholic acid (TCA) in the mice exposed to MC-LR. These findings provide new insights into the roles and mechanisms of MC-LR in susceptible populations, providing a basis for guiding values of MC-LR in drinking water.

Details

Language :
English
ISSN :
2072-6651
Volume :
16
Issue :
5
Database :
MEDLINE
Journal :
Toxins
Publication Type :
Academic Journal
Accession number :
38787064
Full Text :
https://doi.org/10.3390/toxins16050212