摘要
目的采用DNA微点阵(DNAmicroarray)技术检测致癌相关基因的表达水平,研究丙型肝炎病毒(hepatitisCvirus,HCV)非结构蛋白NS4B在HCV致癌中的作用。方法通过建立稳定表达NS4B的细胞系,用微点阵技术研究NS4B对细胞基因表达的影响,实时定量RT-PCR分析微点阵结果中的两个上调基因(DKK1,FYN)和两个下调基因(AKR1C1,v-fos)的表达,对细胞中AKR1C1的活性进行酶学分析。结果在2308个信号途径相关的基因中,34个基因表达上调,56个基因表达下调。在表达有明显差异的基因中,大部分原癌基因表达上调,而大部分抑癌基因的表达下调;一些基因与细胞压力有关。实时定量RT-PCR和AKR1C1的酶学分析进一步证实了DNA微点阵的结果。结论HCV-NS4B在HCV的致癌过程中起一定作用。
Objective The aim was to study the role of NS4B in the carcinogenesis caused by hepatitis C virus(HCV) via detecting the carcinogenesis-associated gene expression using DNA microarray. Methods After stable expressing NS4B cell line established, the influence of NS4B on cellular gene expression profiling was studied using DNA microarray; the expression of two up-regulated and two down-regulated genes from the result of DNA microarray was analyzed via real-time quantitative RT-PCR; the aldo-keto reductase family 1, member C1 (AKR1C1) enzyme activity was analyzed. Results Of the 2 308 genes we examined, 34 were up-regulated and 56 were down-regulated. Oneogenes' expression was mainly up-regulated, whereas tumor suppressors' expression was mainly clown-regulated ; Some involved in cellular stress in these significant different expression genes. The results of DNA microarray were further verified via the analysis of real-time quantitative RT-PCR and AKR1C1 activity. Conclusion The results showed that NS4B might play some roles in the carcinogenesis of HCV.
出处
《中国病原生物学杂志》
CSCD
2006年第2期90-94,共5页
Journal of Pathogen Biology