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吞噬和细胞运动蛋白2对胰腺癌细胞趋化性和转移能力的影响
引用本文:王业成,李鸿雁,孙海晨,张旭,李非.吞噬和细胞运动蛋白2对胰腺癌细胞趋化性和转移能力的影响[J].中华实验外科杂志,2021(1):20-22.
作者姓名:王业成  李鸿雁  孙海晨  张旭  李非
作者单位:首都医科大学宣武医院普通外科;首都医科大学宣武医院外科实验室;首都医科大学宣武医院中心实验室
基金项目:北京市自然科学基金(Z171100001017077);北京市医院管理局临床医学发展专项"扬帆计划"(XMLX201404);首都医科大学科研培育基金(PYZ2018154)。
摘    要:目的:观察吞噬和细胞运动蛋白2(ELMO2)对胰腺癌细胞株人源胰腺癌细胞系-1(PANC-1)的趋化运动能力、细胞黏附能力和侵袭能力的影响,探讨其作用机制。方法:2018年9月至2019年7月应用小干扰RNA技术对PANC-1中ELMO2蛋白进行敲减。采用配对设计方法,分为ELMO2蛋白敲减组、阴性敲减链对照组和空白对...

关 键 词:胰腺癌  趋化性  转移

Effects of engulfment and cell motility 2 protein on chemotaxis and metastasis of pancreatic cancer cells
Wang Yecheng,Li Hongyan,Sun Haichen,Zhang Xu,Li Fei.Effects of engulfment and cell motility 2 protein on chemotaxis and metastasis of pancreatic cancer cells[J].Chinese Journal of Experimental Surgery,2021(1):20-22.
Authors:Wang Yecheng  Li Hongyan  Sun Haichen  Zhang Xu  Li Fei
Institution:(Department of General Surgery,Xuanwu Hospital Capital Medical University,Beijing 100053,China;Surgical Laboratory of Xuanwu Hospital Capital Medical University,Beijing 100053,China;Central Laboratory of Xuanwu Hospital Capital Medical University,Beijing 100053,China)
Abstract:Objective To observe the effects of engulfment and cell motility protein 2(ELMO2)on the chemotactic motility,migration motility,cell adhesion ability and invasion ability of pancreatic cancer cell line pancreatic cancer cell line-1(PANC-1)American type culture collection(ATCC)],and investigate the underlying mechanism.Methods The small interfering RNA technique was used to knock down the ELMO2 protein in the pancreatic cancer cell line PANC-1.The experimental group was designed and PANC-1 cells were transfected with small interfering RNA knockdown strands and negative control strands,respectively,and composed of ELMO2 protein knockdown group,negative control group and normal group.We established concentration gradients of CXC chemokine ligand 12(CXCL12)with different concentrations,and the chemotaxis assay,adhesion assay and cell invasion assay were used to detect the role of ELMO2 on chemotaxis and metastasis of the pancreatic cancer cells.Exogenous co-immunoprecipitation was performed to show the ELMO2 interaction with the Gαi2 subunit.Two-way ANOVAwas used for statistical analysis.Results RNAi interfering strands were transfected into PANC-1 cell line,and the expression of ELMO2 protein in the cells was significantly reduced.After the expression of ELMO2 protein was reduced in PANC-1 cells,when the chemokine concentration was 10μg/L,the number of mobile cells capable of directing transmembrane in the knockdown group was significantly reduced as compared with that in the negative control group(36.67±1.21)vs.(75.67±1.76),t=18.270,P<0.01].Under the condition of chemokine concentration of 10μg/L,the adhesion rate of PANC-1 cells in the ELMO2 knockdown group was significantly lower than that in the negative control group(0.47±0.02)vs(0.79±0.01),t=19.850,P<0.01].When the concentration of chemokine CXCL12 was 10μg/L,the invasion ability of PANC-1 cells in ELMO2 knockdown group was significantly weakened as compared with that in the negative control group(84.33±2.03)vs.(132.00±0.58),t=22.610,P<0.01].A GV362-ELMO2 overexpression plasmid vector was constructed.The band of Gαi2 protein was found in the immunoprecipitation of anti-flag antibody.Conclusion ELMO2 knockdown inhibited chemotaxis,adhesion and invasion of pancreatic cancer cells.Our results confirmed the physical association between ELMO2 and Gαi2 in pancreatic cancer cells through exogenous co-immunoprecipitation.
Keywords:Pancreatic cancer  Chemotaxis  Metastasis
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