[Insulin-like growth factor (IGF)-signalling pathway components are potential therapeutic targets in the treatment of human hepatocellular carcinoma].

T Nussbaum, J Samarin, P Schirmacher, K Breuhahn
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Abstract

The ligand insulin-like growth factor (IGF)-II is highly overexpressed in human hepatocellular carcinoma (HCC) and promotes tumour cell growth. Thus, this signalling axis is a prime target for potential anti-cancer therapies. In this context, gene-specific siRNA against IGF-signalling components as well as IGF1R selective receptor tyrosine kinase (RTK)-inhibitors (tyrphostins) may therefore offer new therapeutic options since both small interfering RNAs (siRNA) and small inhibitory molecules significantly reduce IGFIR signalling in HCC cell lines. However, since highly specific inhibition by siRNA is currently not applicable in the treatment of cancer, selective RTK-inhibitors represent the most promising approach for future therapeutic strategies.

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[胰岛素样生长因子(IGF)信号通路成分是治疗人肝细胞癌的潜在治疗靶点]。
配体胰岛素样生长因子(IGF)-II在人肝细胞癌(HCC)中高度过表达并促进肿瘤细胞生长。因此,这个信号轴是潜在抗癌治疗的主要靶点。在这种情况下,针对igf信号传导成分的基因特异性siRNA以及IGF1R选择性受体酪氨酸激酶(RTK)抑制剂(tyrphostiins)可能因此提供新的治疗选择,因为小干扰rna (siRNA)和小抑制分子都能显著降低HCC细胞系中的IGFIR信号传导。然而,由于siRNA的高度特异性抑制目前不适用于癌症的治疗,选择性rtk抑制剂代表了未来治疗策略中最有希望的方法。
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[The complement system]. [Familial hemophagocytic lymphohistiocytosis]. [Drug-induced liver injury]. Molecular pathology of lung cancer [Chronic myeloproliferative diseases].
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