Smith Maria W, Yue Zhaoxia N, Korth Marcus J, Do Hao A, Boix Loreto, Fausto Nelson, Bruix Jordi, Carithers Robert L, Katze Michael G
Department of Microbiology, School of Medicine, University of Washington, Seattle, WA 98195, USA.
Hepatology. 2003 Dec;38(6):1458-67. doi: 10.1016/j.hep.2003.09.024.
Microarray analysis of RNA from hepatitis C virus (HCV)-infected cirrhotic livers was performed to identify a gene expression signature of liver disease. The expression levels of approximately 13600 genes were analyzed using surgical material and core biopsy specimens from HCV-infected cirrhotic liver explants in comparison with reference samples of normal nondiseased liver. In addition, normal liver samples were compared with each other to determine normal physiologic variation in gene expression. A set of genes, including some associated with stress, acute-phase immune response, and hepatic stellate cell activation, had variable expression levels in normal livers. These genes were subtracted from the sets of genes differentially expressed in cirrhotic livers. To exclude cancer-related genes from our marker sets, we subtracted genes that also were expressed differentially in hepatocellular carcinomas. The resultant HCV- and liver disease-associated gene set provided a molecular portrait of several processes occurring in the HCV-infected liver. It included (1). genes expressed in activated lymphocytes infiltrating the cirrhotic liver, and activated liver macrophages; (2). genes involved in remodeling of extracellular matrix-cell and cell-cell interactions associated with cytoskeleton rearrangements; (3). genes related to the anti-apoptotic pathway of Bcl-2 signaling; and (4). genes involved with the interferon response and virus-host interactions. In conclusion, our microarray analysis identified several potential gene markers of HCV-associated liver disease and contributed to our rapidly expanding database of experiments describing HCV pathogenesis.
对丙型肝炎病毒(HCV)感染的肝硬化肝脏的RNA进行微阵列分析,以确定肝病的基因表达特征。使用来自HCV感染的肝硬化肝脏外植体的手术材料和核心活检标本,与正常无病肝脏的参考样本相比,分析了约13600个基因的表达水平。此外,将正常肝脏样本相互比较,以确定基因表达中的正常生理变异。一组基因,包括一些与应激、急性期免疫反应和肝星状细胞活化相关的基因,在正常肝脏中的表达水平各不相同。这些基因从肝硬化肝脏中差异表达的基因集中被减去。为了从我们的标记集中排除与癌症相关的基因,我们减去了在肝细胞癌中也差异表达的基因。所得的与HCV和肝病相关的基因集提供了在HCV感染的肝脏中发生的几个过程的分子图谱。它包括:(1)在浸润肝硬化肝脏的活化淋巴细胞和活化肝巨噬细胞中表达的基因;(2)参与细胞外基质重塑、与细胞骨架重排相关的细胞-细胞和细胞-细胞相互作用的基因;(3)与Bcl-2信号的抗凋亡途径相关的基因;以及(4)与干扰素反应和病毒-宿主相互作用有关的基因。总之,我们的微阵列分析确定了几种HCV相关肝病的潜在基因标记,并为我们快速扩展的描述HCV发病机制的实验数据库做出了贡献。