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Myricetin Apoptotic Effects on T47D Breast Cancer Cells is a P53-Independent Approach
Mitra Soleimani1, Nayereh Sajedi1
1Department of Anatomical Sciences, Isfahan University of Medical Sciences, Iran.
Objective:
Using nutraceuticals in cancer therapy is a strategy contributing with other approaches to promote apoptosis in cancer cells. Myricetin is a polyphenol flavonoid that forms main ingredients of various type of foods and beverages. The inducing properties of myricetin in apoptosis is reported by several investigations. The present study aimed to assess apoptotic effects of myricetin on T47D breast cancer cells and to evaluate part of the mechanisms of action.
Materials And Methods:
T47D breast cancer cells were assigned into five groups: control (cells in normal condition), myricetin (cells treated with myricetin IC50 concentration) in two different incubation times (24, 48 and 72 hours). MTT assay, annexin v assay, flow cytometry, caspase-3 assay and Real-time PCR were used to evaluate apoptosis in breast cancer cells.
Results:
The expression rate of apoptotic genes caspase-3, caspase-8, caspase-9, the ratio of BAX /Bcl-2 as well as the expression of P53, BRCA1, GADD45 genes were increased significantly after treatment of T47D breast cancer cells with myricetin. Annexin v assay confirmed significant expression of annexin as were displyed by flow cytometry.
Conclusion:
Myricetin enhances apoptosis in T47D breast cancer cells by evoking both extrinsic and intrinsic apoptotic pathways. myricetin may practices its apoptotic properties on T47D cells through inducing BRCA1- GADD45 pathway.
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Insights
Myricetin, a plant flavonoid, effectively induces apoptosis in T47D breast cancer cells. This natural compound activates both extrinsic and intrinsic cell death pathways, offering a potential therapeutic strategy.
Area of Science:
- Oncology
- Molecular Biology
- Natural Product Chemistry
Background:
- Nutraceuticals, including flavonoids like myricetin, are explored for their role in cancer therapy, specifically in inducing cancer cell apoptosis.
- Myricetin, a polyphenol found in various foods and beverages, has demonstrated apoptosis-inducing properties in preliminary studies.
- Understanding the mechanisms by which myricetin affects cancer cells is crucial for its therapeutic application.
Purpose of the Study:
- To investigate the apoptotic effects of myricetin on T47D breast cancer cells.
- To elucidate the molecular mechanisms underlying myricetin-induced apoptosis in this cell line.
Main Methods:
- T47D breast cancer cells were treated with myricetin at its IC50 concentration for 24, 48, and 72 hours.
- Apoptosis was assessed using MTT assay, Annexin V assay, flow cytometry, caspase-3 assay, and Real-time PCR.
- Gene expression analysis focused on apoptosis-related genes including caspases, BAX/Bcl-2 ratio, P53, BRCA1, and GADD45.
Main Results:
- Myricetin treatment significantly increased the expression of apoptosis-related genes: caspase-3, caspase-8, and caspase-9.
- The ratio of BAX/Bcl-2 was significantly altered, indicating a shift towards apoptosis.
- Expression of P53, BRCA1, and GADD45 genes was significantly upregulated, confirmed by Annexin V assay and flow cytometry.
Conclusions:
- Myricetin effectively enhances apoptosis in T47D breast cancer cells.
- The compound activates both extrinsic and intrinsic apoptotic pathways.
- Myricetin may exert its pro-apoptotic effects via the BRCA1-GADD45 pathway.
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