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The cDNA Cloning and Expression of EGFP-PSF Fusion Protein in CHO Cell Line

机译:EGFP-PSF融合蛋白在CHO细胞中的cDNA克隆及表达

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To explore effects of the siRNA of the survivin enhanced tumor sensitivity to chemotherapeutic drugs in human pancreatic cancer cells. A siRNA expression plasmid against the survivin gene were designed, transferred into human pancreatic carcinoma cell line Panc-1 and effected on the cell cycle. After 48 hours transfected, the expression of the survivin gene was inhibited significantly, and arrested the cell cycle in G1 phase, inhibited cell proliferation significantly, and promoted cell apoptosis. The growth of Panc-1 cells was decreased by 62.6% when the Panc-1 cell was transfected with siRNA after 48 hours, in comparison to the control group. Panc-1 cells presented an increase in apoptosis index and in cisplatin sensitivity. Our present results show that Small interfering RNA can exert a knockdown of the survivin gene expression in Panc-1 cells and effectively induce apoptosis and inhibit the growth and increase the chemotherapeutic drug sensitivity of human pancreatic cancer cell line Panc-1.
机译:探索survivin的siRNA的作用增强了人类胰腺癌细胞对化疗药物的敏感性。设计针对survivin基因的siRNA表达质粒,将其转移至人胰腺癌细胞系Panc-1中并影响细胞周期。转染48小时后,survivin基因的表达被显着抑制,并使细胞周期停滞在G1期,显着抑制细胞增殖,并促进细胞凋亡。与对照组相比,当在48小时后用siRNA转染Panc-1细胞时,Panc-1细胞的生长减少了62.6%。 Panc-1细胞的凋亡指数和顺铂敏感性增加。我们目前的结果表明,小分子干扰RNA可以抑制Panc-1细胞中survivin基因的表达,并有效诱导细胞凋亡,抑制其生长,并提高人胰腺癌细胞系Panc-1的化疗药物敏感性。

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