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Gene expression profiling of circulating CD133^+ cells of hepatocellular carcinoma patients associated with HCV infection

机译:HCV感染相关肝癌患者循环CD133 ^ +细胞的基因表达谱

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Aim: Identifying the genetic expression profile of CD133^+ cells from HCC patients compared to CD133^+ cells from healthy volunteers that may contribute in hepatocarcinogenesis process. Method: Circulating CD133^+ cells were sorted from the peripheral blood of HCC patients as well as from healthy volunteers using magnetic activated cell sorting. The differential expression profile of stem cell related genes was performed using the Stem Cell PCR profiling assay. Results: Data analysis of stem cells related genes in CD133^+ cells of the HCC group compared to the control group showed that; CCND2, COL1A1, CTNNA1, DLL3, JAG1, KRT15, MYC, NOTCH2, T and TERT were up-regulated (fold change=80, 68.6, 6.67, 7.22, 3.8, 15.2, 14.5, 105.6, 26.6 and 99 respectively while only CD3D was down-regulated (fold change=0.055) in HCC patients. However, after application of Beferroni correction to adjust P-value; KRT15 was the only gene that was significantly over expressed in CD133^+ cells of HCC compared to control group (P-value=0.012). Conclusion: KRT15 can be used to differentiate between circulating CD133^+ cells from HCC group and control group. However, further study may be needed to confirm on the protein level.
机译:目的:鉴定与健康志愿者的CD133 ^ +细胞相比,HCC患者的CD133 ^ +细胞的基因表达谱,这些基因可能在肝癌的发生过程中起作用。方法:采用磁性激活细胞分选方法,从肝癌患者和健康志愿者的外周血中分选出循环中的CD133 ^ +细胞。干细胞相关基因的差异表达谱使用干细胞PCR分析法进行。结果:与对照组相比,HCC组CD133 ^ +细胞中干细胞相关基因的数据分析表明: CCND2,COL1A1,CTNNA1,DLL3,JAG1,KRT15,MYC,NOTCH2,T和TERT上调(倍数变化分别为80、68.6、6.67、7.22、3.8、15.2、14.5、105.6、26.6和99,而只有CD3D在肝癌患者中被下调(倍数变化= 0.055)。但是,在应用贝弗罗尼校正以调节P值后,与对照组相比,KRT15是肝癌CD133 ^ +细胞中唯一显着过量表达的基因(P -value = 0.012)。结论:KRT15可用于区分HCC组和对照组的循环CD133 ^ +细胞,但仍需要进一步研究以确认其蛋白水平。

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