首页|黄芪皂苷Ⅱ对肾透明细胞癌细胞迁移和侵袭能力的抑制作用及其机制

黄芪皂苷Ⅱ对肾透明细胞癌细胞迁移和侵袭能力的抑制作用及其机制

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目的 探讨黄芪皂苷Ⅱ(ASⅡ)对肾透明细胞癌细胞迁移和侵袭的抑制作用,并分析该作用与Wnt/β-catenin信号通路的关系。方法 取人肾透明细胞癌细胞786-O,随机分为对照组、ASⅡ组和LiCl干预组。对照组仅更换新鲜血清培养基,不进行其他处理;ASⅡ组加入100 μmol/L ASⅡ溶液;LiCl干预组先加入10 mmol/L LiCl(Wnt/β-catenin信号通路激活剂)溶液,24 h后加入100 μmol/L ASⅡ溶液。采用细胞划痕实验观察各组细胞迁移能力,Transwell实验观察细胞侵袭能力,Western blotting法检测细胞上皮间充质转化(EMT)相关蛋白E-钙黏蛋白(E-cadherin)、N-钙黏蛋白(N-cadherin)、波形蛋白(Vimentin)。结果 与对照组比较,ASⅡ组细胞迁移率降低;与ASⅡ组比较,LiCl干预组细胞迁移率升高(P均<0。01)。与对照组比较,ASⅡ组穿膜细胞数减少;与ASⅡ组比较,LiCl干预组穿膜细胞数增加(P均<0。01)。与对照组比较,ASⅡ组E-cadherin蛋白表达水平升高,N-cadherin、Vimentin及β-catenin蛋白表达水平降低;与ASⅡ组比较,LiCl干预组E-cadherin蛋白表达水平降低,N-cadherin、Vimentin及β-catenin蛋白表达水平升高(P均<0。01)。结论 ASⅡ能够抑制肾透明细胞癌细胞的迁移和侵袭能力,其机制可能是通过调控Wnt/β-catenin信号通路来抑制细胞EMT实现的。
Inhibitory effects of astragaloside Ⅱ on invasion and migration of clear cell renal cell carcinoma
Objective To explore the inhibitory effects of astragaloside Ⅱ(ASⅡ)on invasion and migration of clear cell renal cell carcinoma cells,and to analyze the relationships between the effects and Wnt/β-catenin signaling pathway.Methods Human clear cell renal cell carcinoma cells(786-O)were taken and were randomly divided into three groups:the control group,the ASⅡ group,and the LiCl intervention group.In the control group,only fresh serum was used to re-place the culture medium throughout the experiment without any other treatments;in the ASⅡ group,100 μmol/L ASⅡsolution was added to the cells;in the LiCl intervention group,cells were treated with 10 mmol/L LiCl solution,and after 24 h,they were added with 100 μmol/L ASⅡ solution.The migration ability of the cells in each group was measured by Scratch assay,the invasive ability of the cells was detected by Transwell assay,and epithelial-mesenchymal transition(EMT)-related proteins E-cadherin,N-cadherin,and N-cadherin were detected by Western blotting.Results Com-pared with the control group,the cell migration rate decreased in the ASⅡ group;compared with the ASⅡ group,the cell migration rate increased in the LiCl intervention group(both P<0.01).Compared with the control group,the number of transmembrane cells decreased in the ASⅡ group;compared with the ASⅡ group,the number of transmembrane cells in-creased in the LiCl intervention group(both P<0.01).Compared with the control group,the expression level of E-cad-herin protein increased in the ASⅡ group,while the protein expression levels of N-cadherin,Vimentin and β-catenin de-creased.Compared with the ASⅡ group,the expression level of E-cadherin protein in the LiCl intervention group de-creased,while the protein expression levels of N-cadherin,Vimentin and β-catenin increased(all P<0.01).ConclusionsⅡ can inhibit EMT via regulating Wnt/β-catenin signaling pathway.

astragaloside Ⅱkidney neoplasmsWnt/β-catenin signaling pathwaycell migrationcell inva-sionepithelial-mesenchymal transition

赵凯、李勋华、王科

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青岛大学附属医院泌尿外科,山东青岛 266003

黄芪皂苷Ⅱ 肾肿瘤 Wnt/β-catenin信号通路 细胞迁移 细胞侵袭 上皮间充质转化

国家自然科学基金

31971191

2024

山东医药
山东卫生报刊社

山东医药

CSTPCD
影响因子:1.225
ISSN:1002-266X
年,卷(期):2024.64(14)
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