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Peanut Skin Procyanidins reduce the expression of survivin and induce the apoptosis of pancreaticcancer cells through Wnt/ beta-catenin signaling pathway |
MI Wei1, LIU Jinhui1, GUO Mengzhu1, LIU Chengjuan1, TIAN Cheng1, LI Changzhen2, TANG Jinshuo2 |
1 Nutrition and Food Hygiene Section,Public Health and Management College,Binzhou Medical University,Yantai 264003,P.R.China; 2 Clinical Medicine College, Binzhou Medical University |
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Abstract Objective The present work was undertaken to explore the molecular mechanism for the apoptosis of pancreatic cancer cells induced by PSP through down regulating the expression of survivin via the Wnt/β-catenin signal pathway.Methods Pancreatic cancer cells were nurtured routinely at PSP concentrations of 100,200,300,400,500 and 600μg/mL.The cell counting kit-8(CCK-8) assay was used to detect and calculate the inhibitory rate of pancreatic cancer cells after 72 hours of culturing.The IC50 of 450μg/mL was chosen as the experimental group. Western blotting was adopted to detect the degree of GSK-3β and β-catenin phosphorylation and the protein expression levels of survivin, caspase-3 and caspase-7.RT-PCR was used to evaluate the expression level of survivin mRNA.Annexin V-FITC/PI was used to test inhibitory rate of pancreatic cancer cells after 24, 48 and 72 hours.Results The degree of GSK-3β and β-catenin phosphorylation reached the highest (P<0.01) after 12h in the experiment group.The expression of survivin mRNA in the experiment group was significantly lower (P<0.01) compared to that in the control group.Under the action of PSP,the expression of survivin protein was the lowest (P<0.01) after 72 hours while the expression of caspase-3 and caspase-7 protein were the highest(P<0.01)after 72 hours.The apoptosis rate of pancreatic cancer cells increased as the culture period was prolonged,which reached 51.59% (P<0.01) after 72 hours of culture.Conclusion PSP can exert a pro-apoptotic effect on pancreatic cancer cells by reducing the expression level of survivin through the Wnt/β-catenin signal pathway.
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Received: 14 April 2017
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