首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Medicine >Short interfering RNA directed against the GOLPH3 gene enhances the effect of chemotherapy against oral squamous cell carcinoma by regulating Caspase3 Bcl2 and cytochrome-c expression
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Short interfering RNA directed against the GOLPH3 gene enhances the effect of chemotherapy against oral squamous cell carcinoma by regulating Caspase3 Bcl2 and cytochrome-c expression

机译:针对GOLPH3基因的短干扰RNA通过调节Caspase3Bcl2和细胞色素c的表达来增强化学疗法对口腔鳞状细胞癌的作用

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摘要

Growing evidence reported that Golgi phosphoprotein 3 (GOLPH3) was involved in the progression of several human cancers. To determine whether knockout of GOLPH3 enhances the effect of Chemotherapy against cell growth of oral squamous cell carcinoma in vitro. OSCC cells were transfected with Golph3 plasmid, Golph3-RNAi and the relative control plasmids. Transfected Tca-8113 cells treated with cis-Dichlorodiamineplatinum (DDP; 0, 0.05, 0.25, 1.25, 6.25 and 31.25 ug/ml) or Paclitaxe (0, 2, 10, 50, 250 and 1250 nM) or Adriamycin (0, 0.25, 0.5, 1, 2 and 4 ug/ml) for 24 h, respectively, was determined using MTT assay. Apoptosis-related protein expression Cytochrome-C, Caspase3 and Bcl-2 was analyzed by RT-PCR and western blots. Result of MTT showed that Golph3-RNAi transfected Tca-8113 cells enhanced the effect of chemotherapy, and the effect was strengthened with the increasing concentration of drugs, and the Golph3 plasmid transfected Tca-8113 cells showed the opposite effect. RT-PCR and western blots assays revealed that expression of cytochrome-C and caspase3 were up-regulated, while Bcl-2 expression was down-regulated in Golph3-RNAi transfected Tca-8113 cells. Taken together, this study demonstrated that GOLPH3 had potent pro-tumor growth and decreased the effect of Chemotherapy, and its mechanism is primarily via cell anti-apoptosis, down-regulating the expression of cytochrome-C and caspase3, up-regulating Bcl-2 expression.
机译:越来越多的证据表明,高尔基磷蛋白3(GOLPH3)参与了几种人类癌症的进展。确定敲除GOLPH3是否增强化学疗法对口腔鳞状细胞癌体外细胞生长的作用。用Golph3质粒,Golph3-RNAi和相关对照质粒转染OSCC细胞。用顺二氯二胺铂(DDP; 0、0.05、0.25、1.25、6.25和31.25 ug / ml)或紫杉醇(0、2、10、50、250和1250 nM)或阿霉素(0,0.25)处理的转染Tca-8113细胞使用MTT分析法分别测定24小时(0.5、1、2和4 ug / ml)(0.5、1、2和4 ug / ml)。通过RT-PCR和蛋白质印迹分析细胞凋亡相关蛋白的表达细胞色素C,Caspase3和Bcl-2。 MTT结果表明,转染Golph3-RNAi的Tca-8113细胞增强了化疗效果,且随着药物浓度的增加而增强,而转染Golph3的Tca-8113细胞则显示了相反的作用。 RT-PCR和western blots分析显示,在Golph3-RNAi转染的Tca-8113细胞中,细胞色素C和caspase3的表达上调,而Bcl-2的表达下调。两者合计,这项研究表明GOLPH3具有强大的促肿瘤生长能力并降低了化疗的效果,其机制主要是通过细胞抗凋亡,下调细胞色素C和caspase3的表达,上调Bcl-2来实现的。表达。

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