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作 者:刘晓艳[1] 方红[1] 羊正纲[2] 阮黎明[1] 方德仁[1] 丁颖果[1] 王懿娜[1] 张好[1] 蒋筱凌[1]
机构地区:[1]浙江大学医学院附属第一医院皮肤科,杭州310003 [2]浙江大学医学院附属第一医院传染病研究所,杭州310003
出 处:《中华皮肤科杂志》2007年第11期676-679,共4页Chinese Journal of Dermatology
基 金:浙江省教育厅资助项目(20051085)
摘 要:目的构建针对人乙酰肝素酶(HPSE)基因的小干扰RNA(siRNA)及其表达载体,观察其对A375细胞HPSE基因的干扰作用及其对肿瘤细胞体外侵袭的抑制作用。方法设计并构建了重组质粒pRNATU6.1/HPSE-siRNA,转染A375细胞,用实时荧光定量PCR法和蛋白质印迹法分别测定HPSE基因RNA和蛋白水平的表达变化,Matrigel侵袭实验观察A375细胞体外侵袭能力的改变。结果将针对HPSE基因的siRNA的双链寡核苷酸片段正确克隆到pRNATU6.1载体;转染A375细胞,与对照组比较,HPSE-siRNA组HPSE基因和蛋白的表达均明显降低。转染后肿瘤细胞的体外侵袭能力与对照组相比受到明显抑制。结论成功构建了针对HPSE基因的siRNA载体,HPSE-siRNA转染A375细胞可以显著降低细胞HPSE基因和蛋白的表达。Objective To construct the small interfering RNA (siRNA) targeting heparanase gene and its expressing vector, and to observe its interference effect on the expression of heparanase gene and inhibitory effect on the invasive potential of human malignant melanoma A375 cells. Methods Three siRNAs were designed. The recombinant plasmid pRNATU6.1/heparanase-siRNA was designed and constructed. A375 cells were cultured, and transfected with pRNATU6.1/heparanase-siRNA. The cells treated with lipofectamine or Opti-MEM served as the controls. Real-time fluorescence quantitative PCR and Western blot were performed to evaluate the expression of heparanase RNA and protein in these treated A375 cells. The in vitro invasive potential of treated A375 cells was assessed by Matrigel gel assay. Results The siRNA targeting heparanase gene was successfully cloned to the eukaryotic expressing vector pRNATU6.1. The expression levels of both heparanase RNA and protein decreased significantly in siRNA-transfected A375 cells than those in the control cells. The in vitro invasive potential of siRNA-transfected cells was also significantly inhibited as compared with that of the control cells (P 〈 0.01 ). Conclusions The siRNA targeting heparanase gene and its expressing vector are successfully constructed, and the designed siRNAs could significantly decrease the mRNA and protein expression of heparanase in A375 cells.
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