Lysimachia capillipes inhibits proliferation of pancreatic cancer BxPC-3 cells in vitro
Xianjin Yu, Liang Zhou, Yahong He
Abstract
Xianjin Yu, Liang Zhou, Yahong He
Abstract
Objective To investigate the effect of lysimachia capillipes(LC) on proliferation of human pancreatic cancer cell line BxPC-3 in vitro and explore the potential mechanism. Methods BxPC-3 cells were treated by LC in different concentrations of 2, 4, 8, 16, 32, 64 μg/ml for 48 and 72 hours, respectively, using untreated cells as control. The survival rate of BxPC-3 cells was measured by MTT method. The half inhibition concentration (IC50) of LC was determined by drawing growth curve. BxPC-3 cells were treated by LC in the concentration of IC50(LC group), and cell apoptosis and cell cycle were examined by using flow cytometry. The protein expression of PARP and capase-3 was detected by Western blotting. Results LC in the concentration of 8-32 μg/ml inhibited the survival rate of BxPC-3 cells in a dose-dependent manner. After exposure to 15 μg/ml LC for 48 h, the apoptosis rate of BxPC-3 cells was increased [(17.3±0.31)% vs (1.5±0.22)%], but the cell cycle was not affected. The expression of caspase-3 protein was up-regulated [(2207.2±92.0) vs 149.1±10.2] and PARP protein was down-regulated [(36.1±4.8) vs 1593.4±29.7] than control group, and the differences were statistically different (all P value <0.05). Conclusions LC can inhibit the growth of BxPC-3 cells, and the potential mechanism was associated with the induction of cell apoptosis by LC via upregulating caspase-3 protein expression and decompsing PARP protein. Key words: Pancreatic neoplasms; Saponins; Lysimachia capillipes; Apoptosis
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Objective To investigate the effect of lysimachia capillipes(LC) on proliferation of human pancreatic cancer cell line BxPC-3 in vitro and explore the potential mechanism. Methods BxPC-3 cells were treated by LC in different concentrations of 2, 4, 8, 16, 32, 64 μg/ml for 48 and 72 hours, respectively, using untreated cells as control. The survival rate of BxPC-3 cells was measured by MTT method. The half inhibition concentration (IC50) of LC was determined by drawing growth curve. BxPC-3 cells were treated by LC in the concentration of IC50(LC group), and cell apoptosis and cell cycle were examined by using flow cytometry. The protein expression of PARP and capase-3 was detected by Western blotting. Results LC in the concentration of 8-32 μg/ml inhibited the survival rate of BxPC-3 cells in a dose-dependent manner. After exposure to 15 μg/ml LC for 48 h, the apoptosis rate of BxPC-3 cells was increased [(17.3±0.31)% vs (1.5±0.22)%], but the cell cycle was not affected. The expression of caspase-3 protein was up-regulated [(2207.2±92.0) vs 149.1±10.2] and PARP protein was down-regulated [(36.1±4.8) vs 1593.4±29.7] than control group, and the differences were statistically different (all P value <0.05). Conclusions LC can inhibit the growth of BxPC-3 cells, and the potential mechanism was associated with the induction of cell apoptosis by LC via upregulating caspase-3 protein expression and decompsing PARP protein. Key words: Pancreatic neoplasms; Saponins; Lysimachia capillipes; Apoptosis
Key concepts: Apoptosis, Cell cycle, Flow cytometry, Cell growth, IC50, Cell culture, Chemistry, In vitro