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Published on: June 9, 2023
Effects of 4',7-dimethoxyflavanone on cell cycle arrest and apoptosis in human breast cancer MCF-7 cells
Eun Jeong Choi1, Jae In Lee, Gun-Hee Kim
1Plant Resources Research Institute, Duksung Women's University, Seoul, 132-714, Korea.
Abstract:
The present study was designed to investigate the anticancer activity of 4,7-dimethoxyflavanone in vitro. When human breast cancer MCF-7 cells were treated with 4',7-dimethoxyflavanone at various concentrations (1-200 μM) for 24 h, antiproliferative effects were first observed at 1 μM and the IC(50) was 115.62 μM. Conversely, 4',7-dimethoxyflavanone was not cytotoxic (measured as lactate dehydrogenase release in CHO-K1 cells) under the same conditions. MCF-7 cells exposed to the 4',7-dimethoxyflavanone at the IC(50) concentration showed cell cycle arrest and apoptosis. Compared to the respective control level, exposure to 4',7-dimethoxyflavanone resulted in a remarkable increase of small DNA fragments at the sub-G1 phase and an increase in the G2/M phase cell population. Moreover, when 4',7-dimethoxyflavanone treatment caused G2/M phase arrest, an increase in CDK1 together with an increase in cyclin B was observed. Based on these results, 4',7-dimethoxyflavanone may be a useful anticancer agent.
Insights
4
Area of Science:
- Pharmacology
- Biochemistry
- Molecular Biology
Background:
- Flavonoids are plant-derived compounds with diverse biological activities.
- Investigating novel anticancer agents is crucial for effective cancer therapy.
Purpose of the Study:
- To evaluate the in vitro anticancer activity of 4',7-dimethoxyflavanone against human breast cancer cells.
- To determine the mechanism of action of 4',7-dimethoxyflavanone-induced cytotoxicity.
Main Methods:
- Human breast cancer MCF-7 cells and Chinese hamster ovary CHO-K1 cells were used.
- Antiproliferative effects were assessed using various concentrations of 4',7-dimethoxyflavanone.
- Cytotoxicity was measured by lactate dehydrogenase release.
- Cell cycle distribution and apoptosis were analyzed via DNA fragmentation and flow cytometry.
- Expression of CDK1 and cyclin B was examined.
Main Results:
- 4',7-dimethoxyflavanone exhibited antiproliferative effects on MCF-7 cells with an IC(50) of 115.62 μM.
- No significant cytotoxicity was observed in CHO-K1 cells.
- Treatment induced cell cycle arrest at the G2/M phase and apoptosis in MCF-7 cells.
- Increased levels of CDK1 and cyclin B were observed during G2/M phase arrest.
Conclusions:
- 4',7-dimethoxyflavanone demonstrates selective anticancer activity against human breast cancer cells in vitro.
- The compound induces apoptosis and cell cycle arrest, suggesting a potential therapeutic role.
- Further investigation into 4',7-dimethoxyflavanone as an anticancer agent is warranted.
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