期刊文献+

RNAi技术沉默Bcl-xL基因表达对食管癌细胞增殖和侵袭的影响

Effect of RNAi silenced Bcl-xL gene on proliferation and invasion ability of human esophageal cancer cell
下载PDF
导出
摘要 目的探讨RNA干扰(RNAi)技术沉默Bcl-xL基因表达对食管癌细胞增殖和侵袭能力的影响。方法将Bcl-xL小干扰RNA(siRNA)转染食管癌EC109细胞,分别采用荧光实时定量RT-PCR和Western blot方法检测食管癌细胞Bcl-xL mRNA和蛋白,采用软琼脂集落培养试验和Boyden小室模型检测癌细胞增殖和侵袭力。结果与对照组相比,siRNA转染组细胞Bcl-xL mRNA和蛋白水平明显下调(P均<0.05),所形成的软琼脂集落数和穿膜细胞数明显减少(P均<0.05),并均呈浓度依赖性。结论采用RNAi技术沉默Bcl-xL基因表达,可抑制食管癌细胞的增殖和侵袭能力。 Objective To study the effect of RNAi silenced Bcl-xL gene on invasion and proliferation of human esophageal cancer cell.Methods Esophageal cancer cell line ECI09 were transfected with different dose of Bcl-xL siRNA. The Bel-xL mRNA and protein were detected by real time RT-PCR and Western blot, respectively. The anchorage-independent proliferation of cancer cells were determined by colony formation in soft agar. The invasion ability of esophageal cancer cells were evaluated by boyden chamber model.Results The Bcl-xL mRNA and protein of tranfected cell was inhibited signifcanfly in a dose-dependent manner ( P 〈 0.05). Compared with control group, both colony formation in soft agar and cells traversed membrane of transfected cells re- duced significantly in dose-dependent manners,resepectively.Conclusion Silencing Bcl-xL expression by RNAi may inhibit proliferation and invasion ability of esophageal cancer cell.
出处 《山东医药》 CAS 北大核心 2008年第33期23-24,共2页 Shandong Medical Journal
基金 中国博士后科学基金资助项目(2003033547)
关键词 食管肿瘤 RNA干扰 BCL-XL基因 esophageal carcinoma RNA interference Bcl-xL gene
  • 相关文献

参考文献2

二级参考文献16

  • 1张海伟,罗英儒,郑佩娥,文剑明.蛋白激酶C的活性变化对人肝癌细胞增殖及端粒酶表达的影响[J].中国病理生理杂志,2004,20(7):1176-1178. 被引量:3
  • 2Yu Fan Shu Zheng Ze-Feng Xu Jia-Yi Ding.Apoptosis induction with polo-like kinase-1 antisense phosph-orothioate oligodeoxynucleotide of colon cancer cell line SW480[J].World Journal of Gastroenterology,2005,11(29):4596-4599. 被引量:18
  • 3Adamson ED,Minchiotti G,Salomon DS.Cripto:a tumor growth factor and more[J].J Cell Physiol,2002,190(3):267-278.
  • 4Ciardiello F,Kim N,Saeki T,et al.Differential expression of epidermal growth factor-related proteins in human colorectal tumors[J].Proc Natl Acad Sci USA,1991,88(17):7792 -7796.
  • 5Normanno N,De Luca A,Salomon DS,et al.Epidermal growth factor-related peptides as targets for experimental therapy of human colon carcinoma[J].Cancer Detect Prey,1998,22(1):62-67.
  • 6De Angelis E,Grassi M,Gullick WJ,et al.Expression of cripto and amphiregulin in colon mucosa from high risk colon cancer families[J].Int J Oncol,1999,14(3):437-440.
  • 7Baldassarre G,Tucci M,Lembo G,et al.A truncated form of teratocarcinoma-derived growth factor-1 (cripto-1) mRNA expressed in human colon carcinoma cell lines and tumors[J].Tumour Biol,2001,22(5):286-293.
  • 8Tang R,Cheng AJ,Wang JY,et al.Close correlation between telomerase expression and adenomatous polyp progression in multistep colorectal carcinogenesis[ J ].Cancer Res,1998,58(18):4052-4054.
  • 9Engelhardt M,Drullinsky P,Guillem J,et al.Telomerase and telomere length in the development and progression of premalignant lesions to colorectal cancer[J].Clin Cancer Res,1997,3(11):1931-1941.
  • 10Mizumoto I,Ogawa Y,Niiyama H,et al.Possible role of telomerase activation in the multistep tumor progression of periampullary lesions in patients with familial adenomatous polyposis[J].Am J Gastroenterol,2001,96(4):1261-1265.

共引文献79

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部