[Insulin-like growth factor (IGF)-II in human hepatocarcinogenesis--a potential therapeutic target?].

T Nussbaum, S Vreden, M Farsad, P Schirmacher, K Breuhahn
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Abstract

Several studies have examined the expression profiles of human hepatocellular carcinomas (HCCs) using high density microarray technology, but subtyping with potential mechanistic and therapeutic impact has not been achieved so far. Here we have analysed the expression pattern of human HCCs and HCC cell lines in comparison to normal liver. A characteristic of one group of HCCs and all HCC cell lines was overexpression of insulin-like growth factor (IGF)-II. Moreover, IGF-II expression was mutually exclusive to induction of several IFN-related genes. In vitro, treatment of HCC cells with IFNgamma leads to a strong reduction of IGF-II expression. Equally, specific reduction of IGF-II was achieved using RNAinterference in HCC cells. Therefore, IGF-II may represent an excellent target for IFNgamma-treatment and specific siRNA-mediated therapeutic intervention.

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[胰岛素样生长因子(IGF)-II在人肝癌发生中的作用——一个潜在的治疗靶点?]。
一些研究已经使用高密度微阵列技术检测了人类肝细胞癌(hcc)的表达谱,但迄今为止尚未实现具有潜在机制和治疗影响的亚型。在这里,我们分析了人类HCC和HCC细胞系与正常肝脏的表达模式。一组HCC和所有HCC细胞系的一个特征是胰岛素样生长因子(IGF)-II过表达。此外,IGF-II的表达与几种ifn相关基因的诱导是互斥的。在体外,用IFNgamma治疗HCC细胞导致IGF-II表达的强烈降低。同样,在HCC细胞中使用rninterference可以实现IGF-II的特异性降低。因此,IGF-II可能是ifγ治疗和特异性sirna介导的治疗干预的一个极好的靶点。
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