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Ellagic acid inhibits the proliferation of human pancreatic carcinoma PANC-1 cells in vitro and in vivo

机译:鞣花酸在体外和体内抑制人胰腺癌PANC-1细胞的增殖

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摘要

Ellagic aicd (EA), a dietary polyphenolic compound found in plants and fruits, possesses various pharmacological activities. This study investigated the effect of EA on human pancreatic carcinoma PANC-1 cells both in vitro and in vivo; and defined the associated molecular mechanisms. In vitro, the cell growth and repairing ability were assessed by CCK-8 assay and wound healing assay. The cell migration and invasion activity was evaluated by Tanswell assay. In vivo, PANC-1 cell tumor-bearing mice were treated with different concentrations of EA. We found that EA significantly inhibited cell growth, cell repairing activity, and cell migration and invasion in a dose-dependent manner. Treatment of PANC-1 xenografted mice with EA resulted in significant inhibition in tumor growth and prolong mice survival rate. Furthermore, flow cytometric analysis showed that EA increased the percentage of cells in the G1 phase of cell cycle. Western blot analysis revealed that EA inhibited the expression of COX-2 and NF-κB. In addition, EA reversed epithelial to mesenchymal transition by up-regulating E-cadherin and down-regulating Vimentin. In summary, the present study demonstrated that EA inhibited cell growth, cell repairing activity, cell migration and invasion in a dose-dependent manner. EA also effectively inhibit human pancreatic cancer growth in mice. The anti-tumor effect of EA might be related to cell cycle arrest, down-regulating the expression of COX-2 and NF-κB, reversing epithelial to mesenchymal transition by up-regulating E-cadherin and down-regulating Vimentin. Our findings suggest that the use of EA would be beneficial for the management of pancreatic cancer.
机译:Ellagic aicd(EA)是一种在植物和水果中发现的饮食性多酚化合物,具有多种药理活性。这项研究在体外和体内研究了EA对人胰腺癌PANC-1细胞的作用。并定义了相关的分子机制。在体外,通过CCK-8测定和伤口愈合测定来评估细胞生长和修复能力。通过Tanswell测定法评估细胞迁移和侵袭活性。在体内,用不同浓度的EA处理PANC-1细胞肿瘤小鼠。我们发现EA以剂量依赖性方式显着抑制细胞生长,细胞修复活性以及细胞迁移和侵袭。 EA处理PANC-1异种移植小鼠可显着抑制肿瘤生长并延长小鼠存活率。此外,流式细胞仪分析表明,EA增加了细胞周期G1期的细胞百分比。 Western blot分析表明,EA抑制了COX-2和NF-κB的表达。此外,EA通过上调E-钙粘蛋白和下调波形蛋白逆转上皮到间质的转化。总而言之,本研究证明了EA以剂量依赖性方式抑制细胞生长,细胞修复活性,细胞迁移和侵袭。 EA还可以有效抑制小鼠胰腺癌的生长。 EA的抗肿瘤作用可能与细胞周期停滞,下调COX-2和NF-κB的表达,通过上调E-钙粘蛋白和下调波形蛋白逆转上皮到间质的转变有关。我们的研究结果表明,EA的使用对胰腺癌的治疗将是有益的。

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