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RNAi 介导的胰岛素受体底物-4 沉默增强放线菌素 D 和肿瘤坏死因子-α诱导的肝癌细胞系细胞死亡。

RNAi-mediated silencing of insulin receptor substrate-4 enhances actinomycin D- and tumor necrosis factor-alpha-induced cell death in hepatocarcinoma cancer cell lines.

机构信息

Unidad de Toxicología Molecular Hepática, Departamento de Bioquímica y Biología Molecular, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD). Universidad de Alcalá, E-28871 Alcalá de Henares, Spain.

出版信息

J Cell Biochem. 2009 Dec 15;108(6):1292-301. doi: 10.1002/jcb.22359.

Abstract

Insulin receptor substrate-4 (IRS-4) transmits signals from the insulin-like growth factor receptor (IGF-IR) and the insulin receptor (IR) to the PI3K/AKT and the ERK1/2 pathways. IRS-4 expression increases dramatically after partial hepatectomy and plays an important role in HepG2 hepatoblastoma cell line proliferation/differentiation. In human hepatocarcinoma, IRS-4 overexpression has been associated with tumor development. Herein, we describe the mechanism whereby IRS-4 depletion induced by RNA interference (siRNA) sensitizes HepG2 cells to treatment with actinomycin D (Act D) and combined treatment with Act D plus tumor necrosis factor-alpha (TNF-alpha). Similar results have been obtained in HuH 7 and Chang cell lines. Act D therapy drove the cells to a mitochondrial-dependent apoptotic program involving cytochrome c release, caspase 3 activation, PARP fragmentation and DNA laddering. TNF-alpha amplifies the effect of Act D on HepG2 cell apoptosis increasing c-jun N-terminal kinase (JNK) activity, IkappaB-alpha proteolysis and glutathione depletion. IRS-4 depleted cells that were treated with Act D showed an increase in cytochrome c release and procaspase 3 and PARP proteolysis with respect to control cells. The mechanism involved in IRS-4 action is independent of Akt, IkappaB kinase and JNK. IRS-4 down regulation, however, decreased gamma-glutamylcysteine synthetase content and cell glutathione level in the presence of Act D plus TNF-alpha. These results suggest that IRS-4 protects HepG2 cells from oxidative stress induced by drug treatment.

摘要

胰岛素受体底物-4(IRS-4)将胰岛素样生长因子受体(IGF-IR)和胰岛素受体(IR)的信号传递到 PI3K/AKT 和 ERK1/2 途径。部分肝切除术后 IRS-4 的表达显著增加,并在 HepG2 肝癌细胞系增殖/分化中发挥重要作用。在人类肝癌中,IRS-4 的过表达与肿瘤的发展有关。在此,我们描述了 IRS-4 通过 RNA 干扰(siRNA)耗竭使 HepG2 细胞对放线菌素 D(Act D)和 Act D 联合肿瘤坏死因子-α(TNF-α)治疗敏感的机制。在 HuH7 和 Chang 细胞系中也得到了类似的结果。Act D 治疗使细胞进入线粒体依赖性凋亡程序,涉及细胞色素 c 释放、caspase 3 激活、PARP 片段化和 DNA 梯状带。TNF-α 通过增加 c-jun N 末端激酶(JNK)活性、IkappaB-α 蛋白水解和谷胱甘肽耗竭来放大 Act D 对 HepG2 细胞凋亡的作用。用 Act D 处理的 IRS-4 耗竭细胞与对照细胞相比,细胞色素 c 释放和原胱天蛋白酶 3 和 PARP 蛋白水解增加。IRS-4 作用的机制独立于 Akt、IkappaB 激酶和 JNK。然而,在 Act D 加 TNF-α存在的情况下,IRS-4 的下调降低了γ-谷氨酰半胱氨酸合成酶含量和细胞谷胱甘肽水平。这些结果表明,IRS-4 可保护 HepG2 细胞免受药物治疗引起的氧化应激。

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