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李美佳, 王冰, 毛凯平, 渠开攀, 张维娜. 跨膜接头蛋白PAG1过表达对皮肤鳞癌细胞A431运动能力的影响[J]. 肿瘤防治研究, 2016, 43(9): 738-742. DOI: 10.3971/j.issn.1000-8578.2016.09.002
引用本文: 李美佳, 王冰, 毛凯平, 渠开攀, 张维娜. 跨膜接头蛋白PAG1过表达对皮肤鳞癌细胞A431运动能力的影响[J]. 肿瘤防治研究, 2016, 43(9): 738-742. DOI: 10.3971/j.issn.1000-8578.2016.09.002
LI Meijia, WANG Bing, MAO Kaiping, QU Kaipan, ZHANG Weina. Effect of Ectopic Expression of Transmembrane Adaptor PAG1 on Motility of Cutaneous Squamous Cell Carcinoma A431 Cells in vitro[J]. Cancer Research on Prevention and Treatment, 2016, 43(9): 738-742. DOI: 10.3971/j.issn.1000-8578.2016.09.002
Citation: LI Meijia, WANG Bing, MAO Kaiping, QU Kaipan, ZHANG Weina. Effect of Ectopic Expression of Transmembrane Adaptor PAG1 on Motility of Cutaneous Squamous Cell Carcinoma A431 Cells in vitro[J]. Cancer Research on Prevention and Treatment, 2016, 43(9): 738-742. DOI: 10.3971/j.issn.1000-8578.2016.09.002

跨膜接头蛋白PAG1过表达对皮肤鳞癌细胞A431运动能力的影响

Effect of Ectopic Expression of Transmembrane Adaptor PAG1 on Motility of Cutaneous Squamous Cell Carcinoma A431 Cells in vitro

  • 摘要:
    目的  研究跨膜接头蛋白PAG1过表达对人皮肤鳞状细胞癌A431运动能力的影响。
    方法  构建PAG1-EGFP融合蛋白的慢病毒表达载体,采用反转录病毒转染的方法建立PAG1过表达的A431细胞株,实验分为3组:亲本细胞组(未进行基因转染的A431细胞)、对照组(A431细胞转染仅含EGFP阴性对照病毒)、实验组(A431细胞转染PAG1-EGFP病毒)。流式细胞术检测细胞转染率,实时荧光定量PCR及Western blot检测转染后PAG1 mRNA及其蛋白表达,进一步验证细胞转染成功与否;利用划痕修复实验、Transwell迁移实验、侵袭实验三种不同的方法检测PAG1基因的过表达是否会对皮肤鳞癌细胞的生长、迁移和侵袭能力产生影响。
    结果  实验组和对照组目的基因病毒的转染表达率分别为(94.97±0.15)%、(94.60±0.35)%;实验组细胞中PAG1基因mRNA的表达量约为亲本细胞组的1.6倍(P=0.000),转染后实验组中PAG1蛋白的相对表达水平明显增加(P=0.000),建立了稳定过表达PAG1的A431细胞系;PAG1过表达明显降低A431细胞愈合率(P=0.000);实验组A431细胞迁移、侵袭能力明显降低(P=0.001, P=0.000)。
    结论  PAG1的过表达能抑制人皮肤鳞癌细胞运动能力,影响肿瘤的浸润及远处转移。

     

    Abstract:
    Objective  To investigate the effect of the ectopic expression of transmembrane protein PAG1 on the motility of human cutaneous squamous cell carcinoma A431 cells.
    Methods  The PAG1-EGFP lentiviral vector was constructed. A431 cells were transfected with PAG1-EGFP lentiviral vector (Experimental group) or negative-EGFP lenti-viral vector (Control group), or remained untransfected(Parental group). The transfection efficiency was detected by flow cytometry. To further verify and determine the success of the infection, the expression of PAG1 mRNA and protein were detected by real-time fluorescence quantitative PCR and Western blot, respectively. After additional culture, the wound-healing assay and Transwell chamber assay were performed to evaluate the abilities of migration and invasion.
    Results  The transfection efficiency in the experimental group and control group were (94.97±0.15)% and (94.60±0.35)%, respectively. After transfected with PAG1-EGFP vector, the expression of PAG1 mRNA was about 1.6 times enhanced than that of untrasfected cells(P=0.000). The PAG1 protein levels were significantly increased after transfection with PAG1-EGFP lentiviral vector (P=0.000). The A431 cell line with PAG1 overexpression was successfully constructed; the ectopic expression of PAG1 significantly decreased the cells healing rate(P=0.000). Moreover, cell migration and invasion abilities were significantly inhibited(P=0.001, P=0.000).
    Conclusion  The elevated levels of PAG1 could obviously inhibit the mobility of human cutaneous squamous cell carcinoma cells in vitro, which suggesting that the overexpression of PAG1 may influence their metastatic ability in vivo.

     

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