Journal
ANTICANCER RESEARCH
Volume 35, Issue 3, Pages 1285-1290Publisher
INT INST ANTICANCER RESEARCH
Keywords
Apoptosis; breast cancer; tannic acid; tissue engineering
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Funding
- Dabo's All-In Team Foundation
- Avon Foundation for Women
- Clemson University Institute for Biological Interfaces of Engineering
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Background: The naturally-occurring phyto-chemical tannic acid (TA) has anticancer properties. We have demonstrated that estrogen receptor-positive (ER+) breast cancer cells are more sensitive to effects of TA than triple-negative breast cancer cells and normal breast epithelial cells. In the present study, cells were grown on TA-crosslinked collagen beads. Growing cells remodel collagen and release TA, which affects attached cells. Materials and Methods: The ER+ breast cancer cell line MCF7 and the normal breast epithelial cell line MCF10A were grown on TA-crosslinked collagen beads in roller bottles. Concentrations of TA in conditioned media were determined. Induced apoptosis was imaged and quantified. Caspase gene expression was calculated by real-time polymerase chain reaction (PCR). Results: Both cell lines attached and grew on TA-crosslinked collagen beads where they remodeled collagen and released TA into surrounding medium. Released TA induced caspase-mediated apoptosis. Conclusion: TA induced apoptosis in a concentration-dependent manner, with ER+ MCF7 cells displaying more sensitivity to effects of TA.
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