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A Genetically Engineered Mouse Model of Sporadic Colorectal Cancer
Published on: July 6, 2017
Oral administration of yessotoxin stabilizes E-cadherin in mouse colon
Federica Callegari1, Silvio Sosa, Sara Ferrari
1Dipartimento di Scienze Biomediche, Università di Modena e Reggio Emilia, Via G. Campi 287, I-41100 Modena, Italy.
Abstract:
YTX has been shown to disrupt the E-cadherin-catenin system in cultured epithelial cells, raising some concern that ingestion of seafood contaminated by YTX might favour tumour spreading and metastasis formation in vivo. In order to probe whether YTX might affect cadherin systems in vivo, we have set up a study involving repeated oral dosing of the toxin in mice (1mg/kg/day, for 7 days) and analysis of E-cadherin and N-cadherin in tissue extracts obtained at the end of the dosing scheme, as well as 1 and 3 months after YTX administration. We found that the E-cadherin pools obtained from lung and kidney were not altered by YTX in any of our experimental conditions. Extracts from mouse colon contained intact E-cadherin and an E-cadherin fragment of about 90 kDa (ECRA(90)), displaying a molecular alteration resembling that caused by YTX in cultured cells. We found that the relative proportion of ECRA(90), as compared to intact E-cadherin, was higher in colon extracts from control mice than from YTX-treated animals, indicating that oral administration of YTX to mice stabilizes E-cadherin of mouse colon. No significant difference could be detected in samples prepared from colons obtained 30 or 90 days after termination of YTX treatment. Oral administration of YTX to mice did not lead to a significant increase in the fragments of E-cadherin detectable in serum, neither it altered the N-cadherin pool of mouse heart. Electron microscopy analysis showed no substantial ultrastructural differences between controls and YTX-treated mice. Our findings show that ingestion of food contaminated by YTX poses a low risk of disruption of the E-cadherin system in vivo.
Insights
YTX toxin ingestion does not disrupt E-cadherin in mouse lungs or kidneys. Oral YTX administration to mice stabilizes E-cadherin in the colon, posing a low risk for metastasis.
Area of Science:
- Toxicology
- Cell Biology
- Molecular Biology
Background:
- YTX (Yessotoxin) can disrupt the E-cadherin-catenin system in cultured cells.
- Concerns exist regarding YTX-induced tumor spreading and metastasis in vivo.
- Investigating YTX's in vivo effects on cadherin systems is crucial.
Purpose of the Study:
- To determine if YTX affects E-cadherin and N-cadherin systems in vivo.
- To assess the risk of YTX-contaminated seafood ingestion on metastasis.
Main Methods:
- Repeated oral dosing of YTX (1mg/kg/day for 7 days) in mice.
- Analysis of E-cadherin and N-cadherin in tissue extracts (lung, kidney, colon, heart) at various time points.
- Electron microscopy for ultrastructural analysis.
Main Results:
- YTX did not alter E-cadherin in lung or kidney tissues.
- YTX stabilized E-cadherin in mouse colon, reducing a specific fragment (ECRA(90)).
- No significant changes in serum E-cadherin fragments or heart N-cadherin were observed post-YTX treatment.
Conclusions:
- Oral YTX administration poses a low risk for disrupting the E-cadherin system in vivo.
- YTX does not appear to promote tumor spreading or metastasis via cadherin disruption.
- Findings suggest YTX-contaminated seafood is unlikely to enhance metastasis in vivo.