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Gene Expression Differences of TNBG on Human Hepatocellular Carcinoma Cell Line QGY-7701 with cDNA Microarray

机译:用cDNA微阵列对人肝细胞癌细胞系QGY-7701的基因表达差异

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To further investigate the mechanism of TNBG. We used cDNA microarray to explore Gene Expression Difference of TNBG on human hepatocellular carcinoma cell line QGY-7701. After treated with TNBG for 3 days, mRNA from both control and treated cells were isolated and purified to prepare the probes, then reversely transcribed to cDNA with the incorporation of fluore-scent labelled dUTP. The probes were hybridized with a microarray representing the 8464 human cDNAs. The fluorescent signals of Cy3 and Cy5 were scanned and analyzed. We found that the gene expression profiles were changed greatly. Among the 8464 target genes, 1200(14.2%) different expression genes were detected. The 654 genes were down-regulated and the 546 genes were up-regulated. They were functionally related to cell proliferation cycle, replication, metabolism, and so on. The expression difference of some genes involved in lipid biosynthesis, lipid transport, and lipid degradation were extremely significant.
机译:进一步研究TNBG的机制。我们使用cDNA微阵列探索TNBG对人肝细胞癌细胞系QGY-7701的基因表达差异。在用TNBG处理3天后,分离来自对照和处理细胞的mRNA并纯化以制备探针,然后通过掺入荧光香味标记的DUTP掺入cDNA。探针与代表8464人CDNA的微阵列杂交。扫描并分析Cy3和Cy5的荧光信号。我们发现基因表达曲线变化了很大。在8464个靶基因中,检测到1200(14.2%)不同的表达基因。将654个基因进行下调,上调546个基因。它们与细胞增殖循环,复制,新陈代谢等有关。参与脂质生物合成,脂质转运和脂质降解的一些基因的表达差异非常显着。

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