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胰岛素样生长因子 I 受体:肝细胞癌基因治疗的新靶点。

Insulin-like Growth Factor I Receptor: A Novel Target for Hepatocellular Carcinoma Gene Therapy.

机构信息

Medical School of Nantong University, Nantong 226001, China.

Research Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong 226001, Jiangsu, China.

出版信息

Mini Rev Med Chem. 2019;19(4):272-280. doi: 10.2174/1389557518666181025151608.

DOI:10.2174/1389557518666181025151608
PMID:30360707
Abstract

Human insulin-like growth factor (IGF) axis affects the molecular pathogenesis of hepatocellular carcinoma (HCC), especially in the abnormality of hepatic IGF-I receptor (IGF-IR) or IGF-II expression as a key molecule in hepatocarcinogenesis. However, the over-expression of hepatic IGFIR is associated with HCC progression with largely unknown mechanisms. The IGF-IR as one key molecule of the IGF signal pathway plays an important role in the hepatocyte malignant transformation. Attaching importance to IGF-IR might improve the prognostic or the therapeutic technique of HCC. This article reviews IGF-IR alteration during HCC development, and the effects of silencing IGF-IR gene by specific short hairpin RNA on the inhibition of cell proliferation in vitro or HCC xenograft growth in vivo to elucidate it as a novel molecular-targeted therapy for HCC.

摘要

人胰岛素样生长因子 (IGF) 轴影响肝细胞癌 (HCC) 的分子发病机制,特别是在肝 IGF-I 受体 (IGF-IR) 或 IGF-II 表达异常作为肝癌发生的关键分子。然而,肝 IGFIR 的过度表达与 HCC 进展相关,但机制尚不清楚。IGF-IR 作为 IGF 信号通路的一个关键分子,在肝细胞恶性转化中发挥重要作用。重视 IGF-IR 可能会改善 HCC 的预后或治疗技术。本文综述了 IGF-IR 在 HCC 发展过程中的改变,以及特异性短发夹 RNA 沉默 IGF-IR 基因对体外细胞增殖或 HCC 异种移植生长的抑制作用,阐明其作为 HCC 的一种新的分子靶向治疗方法。

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