食品科学 ›› 2022, Vol. 43 ›› Issue (15): 176-184.doi: 10.7506/spkx1002-6630-20220104-021

• 营养卫生 • 上一篇    

连翘苷对食管上皮恶性转变细胞和食管癌Eca-109细胞的抑制作用及机制

郭子琪,王少康,桂兰兰,夏惠,孙桂菊   

  1. (东南大学公共卫生学院,江苏 南京 210009)
  • 发布日期:2022-08-30

Inhibitory Effect and Mechanism of Forsythin on Malignantly Transformed Esophageal Epithelial Cells and Esophageal Cancer Eca-109 Cells

GUO Ziqi, WANG Shaokang, GUI Lanlan, XIA Hui, SUN Guiju   

  1. (School of Public Health, Southeast University, Nanjing 210009, China)
  • Published:2022-08-30

摘要: 目的:探究连翘苷对食管上皮恶性转变细胞和食管癌Eca-109细胞增殖、周期、凋亡、迁移、侵袭的影响,分析其对这两种细胞的抑制效果及其作用机制。方法:取食管上皮恶性转变细胞和食管癌Eca-109细胞,使用不同浓度(10、100 μmol/L)的连翘苷处理干预细胞24 h,采用细胞计数试剂盒-8(cell counting kit-8,CCK8)法检测细胞增殖,流式细胞术检测细胞周期、凋亡,Transwell实验检测细胞迁移、侵袭,蛋白免疫印迹法(Western blotting)检测细胞中磷脂酰肌醇-3-激酶(phosphoinositide 3-kinase,PI3K)、蛋白激酶B(protein kinase B,PKB),(也称为AKT)、磷酸化磷脂酰肌醇3-激酶(phosphorylated phosphatidylinositol-3-kinase,p-PI3K)、磷酸化蛋白激酶B(phosphorylated protein kinase B,p-PKB)(也称为p-AKT)、p21蛋白、B淋巴细胞瘤-2(B-cell lymphoma-2,Bcl-2)和基质金属蛋白酶9(matrix metallopeptidase 9,MMP9)表达水平。结果:连翘苷对食管上皮恶性转变细胞和食管癌Eca-109细胞的半数抑制浓度(50% inhibitory concentration,IC50)分别为308.4 μmol/L和322.0 μmol/L。10、100 μmol/L连翘苷可显著抑制食管上皮恶性转变细胞和Eca-109细胞增殖(P<0.05),对人食管正常上皮细胞无毒性作用。10、100 μmol/L连翘苷可诱导食管上皮恶性转变细胞和Eca-109细胞周期改变,促进细胞凋亡。10、100 μmol/L连翘苷可显著抑制食管上皮恶性转变细胞和Eca-109细胞迁移及侵袭(P<0.05)。10、100 μmol/L连翘苷可显著降低食管上皮恶性转变细胞和Eca-109细胞中p-PI3K、p-AKT、Bcl-2和MMP9蛋白的表达水平(P<0.05),100 μmol/L连翘苷可显著提高食管上皮恶性转变细胞和Eca-109细胞中p21蛋白的表达水平(P<0.05)。结论:连翘苷可显著抑制食管上皮恶性转变细胞和食管癌Eca-109细胞增殖、迁移、侵袭,其机制可能与PI3K/AKT通路失活有关。

关键词: 连翘苷;食管上皮恶性转变细胞;Eca109细胞;PI3K/AKT

Abstract: Objective: The inhibitory effect of forsythin on the proliferation, cell cycle, apoptosis, migration and invasion of malignantly transformed esophageal epithelial cells and esophageal cancer Eca-109 cells was explored, and the underlying mechanism was analyzed. Methods: Malignantly transformed esophageal epithelial cells and Eca-109 cells were treated with 10 and 100 μmol/L forsythin for 24 h. Cell proliferation was detected by cell counting kit-8 (CCK-8). Cell cycle and apoptosis were detected by flow cytometry. Cell migration and invasion were detected by Transwell method. The expression levels of phosphoinositide 3-kinase (PI3K), protein kinase B (PKB, also known as AKT), phosphorylated phosphatidylinositol-3-kinase (p-PI3K), phosphorylated protein kinase B (p-PKB, also knoun as p-AKT), p21, B-cell lymphoma-2 (Bcl-2), and matrix metallopeptidase 9 (MMP9) in cells were detected by Western blotting. Results: The 50% inhibitory concentration (IC50) values of forsythin for malignantly transformed esophageal epithelial cells and Eca-109 cells were 308.4 and 322.0 μmol/L, respectively. Forsythin at 10 and 100 μmol/L could significantly inhibit the proliferation of the two cell lines (P < 0.05), but was nontoxic to normal esophageal epithelial cells. Forsythin at 10 and 100 μmol/L could alter cell cycle, promote cell apoptosis, significantly inhibit cell migration and invasion (P < 0.05), and reduce the expression levels of p-PI3K, p-AKT, Bcl-2 and MMP9 proteins (P < 0.05). Forsythin at 100 μmol/L could significantly increase the expression level of p21 protein in both cell lines (P < 0.05). Conclusion: Forsythin can significantly inhibit the proliferation, migration and invasion of esophageal epithelial malignant transformed cells and Eca-109 cells, and the mechanism may be related to the inactivation of the PI3K/AKT pathway.

Key words: forsythin; malignantly transformed esophageal epithelial cells; Eca-109 cells; phosphatidylinositol-3-kinase/ protein kinase B pathway

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