›› 2012, Vol. 43 ›› Issue (2): 220-224.doi: 10.3969/j.issn.0529-1356.2012.02.013

• 细胞和分子生物学 • 上一篇    下一篇

shRNA抑制SGK1基因表达对人乳腺癌细胞系生物学特性的影响

覃红斌1; 张玲3; 魏蕾3; 张京伟2*    

  1. 1.湖北民族学院医学院组织学胚胎学教研室,湖北 恩施 445000; 2.武汉大学中南医院肿瘤科; 3.武汉大学基础医学院病理学教研室,武汉 430071
  • 收稿日期:2011-09-23 修回日期:2011-11-14 出版日期:2012-04-06
  • 通讯作者: 张京伟

Effect of SGK1 gene inhibition by shRNA on biologic characteristics of the human breast cancer cell

  1. 1.Department of Histology and Embryology,College of Medine,Hubei Institute for Nationalities,Hubei Enshi 445000, China; 2.Department of Oncology,Zhongnan Hospital of Wuhan University; 3.Department of Pathology, College of Medicine, Wuhan University, Wuhan 430071, China
  • Received:2011-09-23 Revised:2011-11-14 Online:2012-04-06
  • Contact: ZHANG Jing-wei

关键词: 乳腺癌, 血清和糖皮质激素调节蛋白激酶, β-catenin, RNA干扰, 免疫印迹法

Abstract: Objective To study the effect of shRNA mediated gene silencing of serum and glucocorticoid induced protein kinase 1(SGK1) on biologic characteristics of human breast cancer cells,MDA-MB-231,and to provide experiment and theoretical evidences for genetic therapy of human breast cancer. Methods Hairpin RNA sequence was synthesized and inserted into pGenesil-3 vector with human U6 promoter.Verified constructs were transfected into MDA-MB-231cells,and then selected by G418.Expression of SGK1 was detected by both real time PCR and Western blotting,and β-catenin expression was detected by Western blotting.MTT growth and matrigel invasion assays were used to study the effect of SGK1 gene silencing.Results Both the mRNA and protein level of SGK1 remarkably decreased after transfection of pGen-3-siSGK1.After gene silencing of SGK1,MDA-MB-231 cells shown strong inhibition of cell growth.The invasive and migratory abilities were inhibited after gene silencing of SGK1.In addition,the change of protein level of β-catenin was consistent with that of SGK1. Conclusion SGK1 inhibition suppresses the growth,invasiveness and migratory abilities of breast cancer cell

Key words: Breast cancer, SGK1, β-catenin, RNA interfering, Western blotting, Human

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