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利用cDNA宏阵列分析鉴定与肝细胞癌病理和病毒学特征相关的不同基因表达谱。

Identification, using cDNA macroarray analysis, of distinct gene expression profiles associated with pathological and virological features of hepatocellular carcinoma.

作者信息

Delpuech Oona, Trabut Jean-Baptiste, Carnot Françoise, Feuillard Jean, Brechot Christian, Kremsdorf Dina

机构信息

INSERM U370, CHU Necker/Institut Pasteur, 75015, Paris, France.

出版信息

Oncogene. 2002 Apr 25;21(18):2926-37. doi: 10.1038/sj.onc.1205392.

DOI:10.1038/sj.onc.1205392
PMID:11973655
Abstract

It is still unclear as to whether the gene expression profile in HCV- or HBV-related HCC exhibits a degree of specificity and whether the development of HCC in a context of cirrhosis influences this gene profile. To address these issues, the expression profiles of 15 cases of HCC were analysed using cDNA macroarray. A global analysis and hierarchical clustering, demonstrated the heterogeneity of HCC patterns, with a majority of down-regulated genes. Statistical analysis clearly showed a distinction between the gene expression profiles of HCV- and HBV-related HCC. HBV-associated HCC exhibited involvement of different cellular pathways, those controlling apoptosis, p53 signalling and G1/S transition. In HCV-related HCC we identified a more heterogenous pattern with an over-expression of the TGF-beta induced gene. In HCC developing on non-cirrhotic tissues, beta-catenin encoding gene and genes implicated in the PKC pathway were specifically up-regulated. In addition, our investigation highlighted a distinct profiles of TGF-beta superfamily encoding genes in well, moderately or poorly differentiated HCC. Overall, our study supports the hypothesis that despite the heterogeneity of the HCC pattern, the large-scale screening of gene expression may provide data significant to our understanding of the mechanism of liver carcinogenesis.

摘要

目前仍不清楚丙型肝炎病毒(HCV)或乙型肝炎病毒(HBV)相关肝癌中的基因表达谱是否具有一定程度的特异性,以及在肝硬化背景下肝癌的发生是否会影响这种基因谱。为了解决这些问题,我们使用cDNA宏阵列分析了15例肝癌的表达谱。整体分析和层次聚类显示了肝癌模式的异质性,大多数基因下调。统计分析清楚地表明HCV相关肝癌和HBV相关肝癌的基因表达谱之间存在差异。HBV相关肝癌表现出不同细胞途径的参与,这些途径控制细胞凋亡、p53信号传导和G1/S期转换。在HCV相关肝癌中,我们发现了一种更具异质性的模式,其中TGF-β诱导基因过度表达。在非肝硬化组织中发生的肝癌中,β-连环蛋白编码基因和与PKC途径相关的基因特异性上调。此外,我们的研究突出了在高分化、中分化或低分化肝癌中TGF-β超家族编码基因的不同谱。总体而言,我们的研究支持这样一种假设,即尽管肝癌模式具有异质性,但基因表达的大规模筛选可能为我们理解肝癌发生机制提供重要数据。

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