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MOMAST® Downregulates AQP3 Expression and Function in Human Colon Cells.
Ines Angelini1, Mariangela Centrone1, Giusy Rita Caponio1
1Department of Biosciences, Biotechnologies, and Environment, University of Bari "Aldo Moro", 70125 Bari, Italy.
Antioxidants (Basel, Switzerland)
|January 25, 2025
Summary
MOMAST®, an olive wastewater complex, reduces colon cell viability and AQP3 expression. This antioxidant inhibits glycerol and H2O2 uptake, suggesting potential for colon disease treatment.
Area of Science:
- Cell Biology
- Molecular Biology
- Gastroenterology
Background:
- Aquaglyceroporin 3 (AQP3) facilitates water, glycerol, and hydrogen peroxide transport in human colon cells.
- Aberrant AQP3 expression is linked to diseases with abnormal cell growth and proliferation.
- MOMAST®, a patented antioxidant from olive wastewater, is investigated for its effects on colon cells.
Purpose of the Study:
- To evaluate the effects of MOMAST® on human colon HCT8 cells.
- To investigate MOMAST®'s impact on AQP3 expression and function.
- To explore MOMAST®'s potential as an adjuvant therapy for colon diseases.
Main Methods:
- Cell viability assays were performed on HCT8 cells treated with MOMAST®.
- Confocal microscopy and Western Blotting were used to assess AQP3 expression.
- Functional studies measured glycerol and H2O2 uptake, alongside epithelial-mesenchymal transition (EMT) markers.
Main Results:
- MOMAST® treatment reduced HCT8 cell viability.
- Significant downregulation of AQP3 expression and protein levels was observed.
- MOMAST® decreased glycerol and H2O2 uptake, and reduced levels of EMT markers like vimentin and β-catenin.
Conclusions:
- MOMAST® effectively reduces colon cell viability and AQP3-mediated transport.
- The observed decrease in AQP3 correlates with reduced glycerol and H2O2 uptake.
- MOMAST® shows promise as an adjuvant therapy for colon diseases characterized by abnormal cell growth, by targeting AQP3.
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