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RNA干扰沉默神经型钙黏素基因对人食管 癌细胞系EC9706侵袭能力的影响
引用本文:何炜,李克,王鑫,林娜,樊青霞.RNA干扰沉默神经型钙黏素基因对人食管 癌细胞系EC9706侵袭能力的影响[J].肿瘤防治研究,2009,36(5):368-371.
作者姓名:何炜  李克  王鑫  林娜  樊青霞
作者单位:郑州大学第一附属医院肿瘤科,450052
基金项目:河南省科技厅科技攻关资助项目 
摘    要: 探讨RNAi沉默N-cadherin基因表达对人食管癌细胞系EC9706体外侵袭能力的影响。方法 将N-cadherin基因的RNA干扰载体pMSCVneo/N-cadherin质粒通过脂质体转染法转染人食管癌细胞系EC9706,运用G418进行抗性克隆的筛选和扩增,进而得到稳定转染的人食管癌细胞系EC9706,通过RT-PCR和Western blot检测稳定转染后的人食管癌细胞系EC9706中N-cadherin的mRNA和蛋白表达水平的变化,同时检测转染前后食管癌细胞系EC9706中MMP-9基因表达水平的变化,并通过Transwell小室体外侵袭实验检测转染前后人食管癌细胞系EC9706体外侵袭能力的变化。结果 通过G418加压筛选法得到稳定转染的人食管癌细胞系EC9706,RT-PCR和Western blot检测结果显示,稳定转染后的人食管癌细胞系EC9706中N-cadherin的mRNA和蛋白表达水平均下调,同时MMP-9基因的mRNA表达水平也随之下调;Transwell小室体外侵袭实验结果显示,伴随着N-cadherin和MMP-9表达水平的下调,人食管癌细胞系EC9706的体外侵袭能力也降低(P<0.05)。结论 RNA干扰沉默神经型钙黏素基因可以使人食管癌细胞系EC9706的体外侵袭能力降低。

关 键 词:食管鳞癌  RNA干扰  N-cadherin  EC9706
收稿时间:2008-4-22
修稿时间:2008-5-29

Effect of RNA Mediated Gene Silencing of N-cadherin Expression on Invasiveness of EC9706
HE Wei,LI Ke,WANG Xin,LIN Na,FAN Qing-xia.Effect of RNA Mediated Gene Silencing of N-cadherin Expression on Invasiveness of EC9706[J].Cancer Research on Prevention and Treatment,2009,36(5):368-371.
Authors:HE Wei  LI Ke  WANG Xin  LIN Na  FAN Qing-xia
Institution:Department of Oncology,The First Affiliated Hospital,Zhengzhou University,Zhengzhou 450052,China
Abstract:Objective To investigate cell invasive power of human EC9706 cell line when the N-cadherin expression was down-regulated by RNA interference (RNAi) technology. Methods N- cadherin shRNA was transfected into EC9706 cells to inhibit the expression of N-cadherin. The effect of RNAi was detected by RT-PCR and Western blot. The invasive ability of the cancer cells was determined by Transwell assay. Results After RNAi,the expression of N-cadherin was significantly decreased, which indicated that RNAi was effective. With the decreased expression of N-cadherin and MMP-9,cell invasiveness was dramatically depressed. Conclusion The down-regulation of N-cadherin protein could impair the invasivness of EC9706 cell line.
Keywords:N-cadherin  EC9706
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