首页> 外文会议>The 1st International Conference on Bioinformatics and Biomedical Engineering(iCBBE 2007) >Downregulation of AFP Protein Expression By RNAi Inhibits the Growth of AFP-producing Gastric Adenocarcinoma Cell Line
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Downregulation of AFP Protein Expression By RNAi Inhibits the Growth of AFP-producing Gastric Adenocarcinoma Cell Line

机译:RNAi对AFP蛋白表达的下调抑制了产生AFP的胃腺癌细胞株的生长

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Many studies have examined the biological activities of Alpha-fetoprotein (AFP); however, the modulatory role of AFP in neoplastic growth remains unclear. Three hairpin siRNA expressing plasmids (pSIREN-DNR-DsRed-Express Donor-Vect or-AFP-siRNA1/2/3) were constructed and transfected into FU97(AFP-producing gastric adenocarcinoma cell line). At 48h after transfection, the silencing efficiency to AFP gene expression was analyzed by RT-PCR and immunoassays. The influence to FU97 on its growth and apoptosis after silencing the AFP gene were observed by MTT and flow cytometry. The results of RT-PCR and immunoassays showed that the plasmids could inhibit AFP mRNA and protein expression at 48h after transfection. The pSIREN-DNR-DsRed-Express Donor Vector-AFP-siRNA1 was more effective than other two. These plasmids could obviously inhibit FU97 cell growth and promote FU97 cell apoptosis.
机译:许多研究已经检查了甲胎蛋白(AFP)的生物学活性。然而,尚不清楚AFP在肿瘤生长中的调节作用。构建了三个发夹siRNA表达质粒(pSIREN-DNR-DsRed-Express Donor-Vect或-AFP-siRNA1 / 2/3),并将其转染到FU97(产生AFP的胃腺癌细胞系)中。转染后48小时,通过RT-PCR和免疫测定分析对AFP基因表达的沉默效率。通过MTT和流式细胞术观察到沉默AFP基因后对FU97对其生长和凋亡的影响。 RT-PCR和免疫分析结果表明,该质粒在转染后48h能抑制AFP mRNA和蛋白表达。 pSIREN-DNR-DsRed-Express供体载体-AFP-siRNA1比其他两个更为有效。这些质粒可以明显抑制FU97细胞的生长并促进FU97细胞的凋亡。

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