Huang Wen-Sheng, Peng Hui, Tan Ming, Ma Jin-Ping, Wang Jian-Ping, Lan Ping
Department of Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.
Zhonghua Wei Chang Wai Ke Za Zhi. 2009 May;12(3):301-5.
To observe the gene silencing and disruption of WNT pathway mediated by the specific shRNA targeted against beta-catenin and its effect on cell proliferation of the human colon cancer cell line Colo205.
The shRNA plasmid vectors against beta-catenin were constructed and transfected into Colo205 cells with Lipofectamine 2000. The expression of beta-catenin was detected by RT-PCR and Western blot. Immunofluorescence staining was also performed to detect the beta-catenin protein expression in cells. The cell proliferation inhibition was determined by MTT assay and soft agar colony formation assay.
The shRNA vectors targeted against beta-catenin were successfully constructed and efficiently suppressed the expression of beta-catenin mRNA and protein(P<0.05). The expression inhibition rates were 47.89% and 45.26% at the mRNA and protein level respectively. Immunofluorescence microscopy also demonstrated the inhibition of beta-catenin protein induced by these specific shRNAs. The MTT assay indicated that the specific shRNA resulted in significant inhibition of cell growth on the culture plates in time-dependent manner. At 72 h post-transfection, the cell viability of CAT group was 48.5%, which was significantly different as compared with that of blank control group's 91.3%(P<0.05). In the soft agar, there were 9, 46, 43 cell colonies in the CAT, blank, and negative control groups respectively, which were significantly different(P<0.05).
The specific shRNAs targeted against beta-catenin has a gene silencing effect and blocks the WNT signaling pathway, which can inhibit the growth of Colo205 cells.
观察针对β-连环蛋白的特异性短发夹RNA(shRNA)介导的WNT信号通路基因沉默和阻断及其对人结肠癌细胞系Colo205细胞增殖的影响。
构建针对β-连环蛋白的shRNA质粒载体,并用Lipofectamine 2000转染Colo205细胞。通过逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹法检测β-连环蛋白的表达。还进行免疫荧光染色以检测细胞中β-连环蛋白的蛋白表达。通过噻唑蓝(MTT)比色法和软琼脂集落形成试验测定细胞增殖抑制情况。
成功构建了针对β-连环蛋白的shRNA载体,有效抑制了β-连环蛋白mRNA和蛋白的表达(P<0.05)。mRNA和蛋白水平的表达抑制率分别为47.89%和45.26%。免疫荧光显微镜检查也证实了这些特异性shRNAs对β-连环蛋白蛋白的抑制作用。MTT试验表明,特异性shRNA以时间依赖性方式显著抑制培养板上的细胞生长。转染后72小时,CAT组的细胞活力为48.5%,与空白对照组的91.3%相比有显著差异(P<0.05)。在软琼脂中,CAT组、空白对照组和阴性对照组分别有9个、46个和43个细胞集落,差异有统计学意义(P<0.05)。
针对β-连环蛋白的特异性shRNAs具有基因沉默作用,可阻断WNT信号通路,抑制Colo205细胞的生长。