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Gene expression profiling of taxol-resistant nasopharyngeal carcinoma cells with siRNA-mediated FOLR1 downregulation

机译:siRNA介导的FOLR1下调对紫杉醇耐药鼻咽癌细胞的基因表达谱分析

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摘要

Objectives: Our previous study has shown that downregulation of FOLR1 by siRNA partially reversed taxol-resistant phenotype in taxol-resistant nasopharyngeal carcinoma cell lines. We aim to gain further insight into the molecular mechanisms of this process and identify the differentially expressed genes after FOLR1 downregulation. Method: The global gene expression profile was identified and analyzed using the Affymetrix HG-U133 Plus 2.0 array. Results: There was a significant dysregulation in the global gene expression of the FOLR1-suppressed taxol-resistant nasopharyngeal carcinoma cell lines. There were 41 upregulated genes and 109 downregulated genes. QRT-PCR validation of the selected differentially expressed genes demonstrated there was a good correlation with the microarray analysis. There was a significant deregulation of expression in the apoptosis-related genes such as BIRC3, PRKX, TNFRSF10A and involved in Viral carcinogenesis, MAPK signaling pathways after FOLR1 was downregulated. Conclusion: The suppression of FOLR1 by RNA interference altered gene expression profile of taxol-resistant nasopharyngeal carcinoma cell lines. The apoptosis-related genes and the gene alterations in viral carcinogenesis, MAPK signaling pathways might be important in FOLR1 siRNA-induced taxol-resistant reversal.
机译:目的:我们以前的研究表明,siRNA下调FOLR1可以部分逆转紫杉醇耐药性鼻咽癌细胞系中的紫杉醇耐药性表型。我们旨在进一步了解这一过程的分子机制,并确定FOLR1下调后差异表达的基因。方法:使用Affymetrix HG-U133 Plus 2.0阵列鉴定并分析了全局基因表达谱。结果:FOLR1抑制紫杉醇耐药的鼻咽癌细胞系的全球基因表达有明显失调。有41个上调基因和109个下调基因。所选差异表达基因的QRT-PCR验证表明与微阵列分析有很好的相关性。凋亡相关基因如BIRC3,PRKX,TNFRSF10A的表达显着下调,并与FOLR1下调后的病毒致癌作用,MAPK信号通路有关。结论:RNA干扰抑制FOLR1改变了紫杉醇耐药鼻咽癌细胞株的基因表达谱。凋亡相关基因和病毒癌变,MAPK信号通路中的基因改变可能在FOLR1 siRNA诱导的紫杉醇耐药逆转中起重要作用。

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