De Giorgi Valeria, Monaco Alessandro, Worchech Andrea, Tornesello Marialina, Izzo Francesco, Buonaguro Luigi, Marincola Francesco M, Wang Ena, Buonaguro Franco M
Molecular Biology and Viral Oncogenesis & AIDS Refer, Center, Ist, Naz, Tumori Fond, G Pascale, Naples, Italy.
J Transl Med. 2009 Oct 12;7:85. doi: 10.1186/1479-5876-7-85.
Hepatitis C virus (HCV) infection is a major cause of hepatocellular carcinoma (HCC) worldwide. The molecular mechanisms of HCV-induced hepatocarcinogenesis are not yet fully elucidated. Besides indirect effects as tissue inflammation and regeneration, a more direct oncogenic activity of HCV can be postulated leading to an altered expression of cellular genes by early HCV viral proteins. In the present study, a comparison of gene expression patterns has been performed by microarray analysis on liver biopsies from HCV-positive HCC patients and HCV-negative controls.
Gene expression profiling of liver tissues has been performed using a high-density microarray containing 36'000 oligos, representing 90% of the human genes. Samples were obtained from 14 patients affected by HCV-related HCC and 7 HCV-negative non-liver-cancer patients, enrolled at INT in Naples. Transcriptional profiles identified in liver biopsies from HCC nodules and paired non-adjacent non-HCC liver tissue of the same HCV-positive patients were compared to those from HCV-negative controls by the Cluster program. The pathway analysis was performed using the BRB-Array- Tools based on the "Ingenuity System Database". Significance threshold of t-test was set at 0.001.
Significant differences were found between the expression patterns of several genes falling into different metabolic and inflammation/immunity pathways in HCV-related HCC tissues as well as the non-HCC counterpart compared to normal liver tissues. Only few genes were found differentially expressed between HCV-related HCC tissues and paired non-HCC counterpart.
In this study, informative data on the global gene expression pattern of HCV-related HCC and non-HCC counterpart, as well as on their difference with the one observed in normal liver tissues have been obtained. These results may lead to the identification of specific biomarkers relevant to develop tools for detection, diagnosis, and classification of HCV-related HCC.
丙型肝炎病毒(HCV)感染是全球肝细胞癌(HCC)的主要病因。HCV诱导肝癌发生的分子机制尚未完全阐明。除了作为组织炎症和再生的间接影响外,可以推测HCV具有更直接的致癌活性,导致早期HCV病毒蛋白使细胞基因表达发生改变。在本研究中,通过微阵列分析对HCV阳性HCC患者和HCV阴性对照的肝活检组织进行了基因表达模式比较。
使用包含36000个寡核苷酸的高密度微阵列对肝组织进行基因表达谱分析,这些寡核苷酸代表了90%的人类基因。样本取自那不勒斯INT医院收治的14例HCV相关HCC患者和7例HCV阴性非肝癌患者。通过Cluster程序将HCV阳性患者HCC结节及配对的非相邻非HCC肝组织的肝活检组织中鉴定出的转录谱与HCV阴性对照的转录谱进行比较。使用基于“ Ingenuity系统数据库”的BRB-Array-Tools进行通路分析。t检验的显著性阈值设定为0.001。
与正常肝组织相比,在HCV相关HCC组织以及非HCC对应组织中,几种属于不同代谢和炎症/免疫通路的基因的表达模式存在显著差异。在HCV相关HCC组织和配对的非HCC对应组织之间仅发现少数基因差异表达。
在本研究中,已获得关于HCV相关HCC和非HCC对应组织的整体基因表达模式及其与正常肝组织中观察到的基因表达模式差异的信息性数据。这些结果可能有助于识别与开发HCV相关HCC检测、诊断和分类工具相关的特定生物标志物。