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机构地区:[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]武汉大学基础医学院病理学教研室,武汉430071 [3]武汉大学中南医院肿瘤科
出 处:《解剖学报》2012年第2期220-224,共5页Acta Anatomica Sinica
基 金:湖北省自然科学基金资助项目(2008CDB222)
摘 要:目的建立稳定抑制血清和糖皮质激素调节蛋白激酶1(SGK1)表达的人乳腺癌细胞系MDA-MB-231,观察SGK1基因沉默对人乳腺癌细胞生物学特性的影响。方法构建针对SGK1的shRNA干扰质粒pGen-3-siSGK1和阴性对照质粒pGen-3-control。转染人乳腺癌细胞系MDA-MB-231,经G418筛选得到稳定抑制SGK1表达的乳腺癌细胞模型;实时定量PCR、免疫荧光以及Western blotting检测shRNA干扰组、阴性对照组及未转染组细胞中SGK1的表达;四甲基偶氮唑盐(MTT)比色法检测细胞体外生长能力;体外浸润实验、细胞迁移实验检测各组癌细胞的侵袭和转移。结果成功构建针对SGK1基因的shRNA干扰质粒,建立了稳定抑制SGK1表达的乳腺癌细胞模型;与阴性对照组和未转染组相比,肿瘤细胞中SGK1的表达水平显著降低(P<0.01);SGK1基因沉默后,人乳腺癌细胞的生长能力、浸润和迁移能力均明显降低(P<0.05)。实验中还发现抑制SGK1基因表达之后,β-catenin的含量也出现明显下降。结论抑制SGK1基因的表达可以显著抑制人乳腺癌细胞MDA-MB-231的生长,并降低其侵袭转移的能力,其中β-catenin参与了SGK1基因的抑制功能。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-231 cells, and then selected by G418. Expression of SGK1 was detected by both real time PCR and Western blotting, and β-eatenin 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 transfeetion 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 cells,and β-eatenin may be involved in this process.
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
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