Tea pigments induce cell-cycle arrest and apoptosis in HepG2 cells

来源 :World Journal of Gastroenterology | 被引量 : 0次 | 上传用户:langjitianya198411
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AIM:To investigate the molecular mechanisms by which tea pigments exert preventive effects on liver carcinogenesis. METHODS:HepG2 cells were seeded at a density of 5x10~5/well in six-well culture dishes and incubated overnight. The cells then were treated with various concentrations of tea pigments over 3 d, harvested by trypsinization, and counted using a hemocytometer. Flow cytometric analysis was performed by a flow cytometer after propidium iodide labeling. Bcl-2 and p21~(WAF1) proteins were determined by Western blotting. In addition, DNA laddering assay was performed on treated and untreated cultured HepG2 cells. RESULTS:Tea pigments inhibited the growth of HepG2 cells in a dose-dependent manner. Flow-cytometric analysis showed that tea pigments arrested cell cycle progression at G_1 phase. DNA laddering was used to investigate apoptotic cell death, and the result showed that 100 mg/L of tea pigments caused typical DNA laddering. Our study also showed that tea pigments induced upregulation of p21~(WAF1) protein and downregulation of Bcl-2 protein. CONCLUSION:Tea pigments induce cell-cycle arrest and apoptosis. Tea pigments may be used as an ideal chemopreventive agent. To investigate the molecular mechanisms by which tea pigments exert preventive effects on liver carcinogenesis. METHODS: HepG2 cells were seeded at a density of 5x10-5 / well in six-well culture dishes and incubated overnight. The cells then were treated with various concentrations of tea pigments over 3 d, harvested by trypsinization, and counted using a hemocytometer. Flow cytometric analysis was performed by a flow cytometer after propidium iodide labeling. Bcl-2 and p21 WAF1 proteins were determined by Western blotting. , DNA laddering assay was performed on treated and untreated cultured HepG2 cells. RESULTS: Tea pigments inhibited the growth of HepG2 cells in a dose-dependent manner. Flow-cytometric analysis showed that tea pigment arrested cell cycle progression at G_1 phase. DNA laddering was used to investigate apoptotic cell death, and the result showed that 100 mg / L of tea pigments caused typical DNA laddering. Our study also showed that tea pigments induced up regulation of p21 WAF1 protein and downregulation of Bcl-2 protein. CONCLUSION: Tea pigments induce cell-cycle arrest and apoptosis. Tea pigments may be used as an ideal chemopreventive agent.
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