Abstract |
In the present study, the in vitro cytotoxicity of daidzein was evaluated in human BEL-7402, A549, HeLa, HepG-2 and MG-63 cancer cell lines. BEL-7402 cells were sensitive to daidzein treatment, with an IC50 value of 59.7±8.1 µM. Daidzein showed no cytotoxic activity toward A549, HeLa, HepG-2 and MG-63 cells. Daidzein increased the levels of reactive oxygen species (ROS) and induced a decrease in mitochondrial membrane potential. Morphological and comet assays showed that daidzein effectively induced apoptosis in BEL-7402 cells. Additionally, daidzein caused cell cycle arrest at the G2/M phase in the BEL-7402 cell line. Daidzein downregulated the expression of Bcl-2, Bcl-x and Baid proteins and upregulated the levels of Bim protein in the BEL-7402 cells. The results demonstrated that daidzein induced BEL-7402 cell apoptosis through an ROS-mediated mitochondrial dysfunction pathway.
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Authors | Bing-Jie Han, Wei Li, Guang-Bin Jiang, Shang-Hai Lai, Cheng Zhang, Chuan-Chuan Zeng, Yun-Jun Liu |
Journal | Oncology reports
(Oncol Rep)
Vol. 34
Issue 3
Pg. 1115-20
(Sep 2015)
ISSN: 1791-2431 [Electronic] Greece |
PMID | 26178389
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Isoflavones
- Phytoestrogens
- Proto-Oncogene Proteins c-bcl-2
- Reactive Oxygen Species
- daidzein
- Caspases
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Topics |
- Apoptosis
(drug effects)
- Blotting, Western
- Caspases
(biosynthesis)
- Cell Cycle Checkpoints
(drug effects)
- Cell Line, Tumor
- Cell Proliferation
(drug effects)
- Comet Assay
- Flow Cytometry
- Humans
- In Vitro Techniques
- Isoflavones
(pharmacology)
- Membrane Potential, Mitochondrial
(drug effects)
- Phytoestrogens
(pharmacology)
- Proto-Oncogene Proteins c-bcl-2
(biosynthesis)
- Reactive Oxygen Species
(metabolism)
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