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Exposure to Microcystin-LR Promotes Colorectal Cancer Progression by Altering Gut Microbiota and Associated Metabolites in APC min/+ Mice.
- Source :
-
Toxins [Toxins (Basel)] 2024 Apr 30; Vol. 16 (5). Date of Electronic Publication: 2024 Apr 30. - Publication Year :
- 2024
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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&#95;XIII&#95;AD3011&#95;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&#95;XIII&#95;AD3011&#95;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.
- Subjects :
- Animals
Mice
Adenomatous Polyposis Coli Protein genetics
Adenomatous Polyposis Coli Protein metabolism
Bile Acids and Salts metabolism
Disease Progression
Dysbiosis chemically induced
Mice, Inbred C57BL
Colorectal Neoplasms pathology
Colorectal Neoplasms chemically induced
Colorectal Neoplasms metabolism
Gastrointestinal Microbiome drug effects
Marine Toxins
Microcystins toxicity
Subjects
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