NOR1增强CB1954诱导的HepG2细胞毒性依赖于Grb2介导的MAPK通路

R. Gui, Jing Liu, Deng-qing Li, Hua Tang, Zhenqian Feng, X. Nie
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引用次数: 1

摘要

硝基还原酶基因NOR1可能参与了肝癌和鼻咽癌的化学致癌作用。我们已经证明,NOR1过表达可以通过减少CB1954的4-硝基基团并增强鼻咽癌(NPC)细胞系CNE1的细胞杀伤能力,将单功能烷基化剂CB1954 ([5-aziridin-1-yl]-2,4-二硝基苯酰胺)转化为有毒形式。然而,其机制尚不清楚。利用cDNA芯片和实时荧光定量PCR技术,我们发现NOR1使肝癌细胞HepG2中Grb2 mRNA的表达增加了4.8倍。在本研究中,我们发现NOR1使Grb2蛋白的表达增加了3倍,并增强了CB1954诱导的HepG2细胞的杀伤作用,并且可以通过添加酪氨酸激酶抑制剂基因蛋白或稳定转染Grb2 shRNA (pU6+27-shGrb2)沉默Grb2的表达来抑制细胞毒性。Western blot分析显示,Grb2的下调可降低MAPK的活性。此外,MEK抑制剂PD98059抑制MAPK的激活可以抑制CB1954诱导的细胞杀伤。这些结果表明,NOR1基因通过上调HepG2细胞中Grb2的表达和激活MAPK信号转导,增强了CB1954细胞的毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NOR1 Enhanced CB1954 Induced Cell Cytotoxicity in HepG2 Is Dependent on Grb2 Mediated MAPK Pathway
Nitroreductase gene NOR1 is possibly involved in the chemical carcinogenesis of hepatic cancer and nasopharyngeal carcinoma. We have demonstrted that NOR1 overexpression could convert monofunction alalkylating agent, CB1954 ([5-aziridin-1-yl]-2,4-dinitrobenzamide) into a toxic form by reduction of the 4-nitro group of CB1954 and enhancing cell killing in nasopharyngeal carcinoma(NPC) cell line CNE1. However, the mechanisms are not known.Using cDNA microarrys and quantitative Real-time PCR, we previously found that NOR1 increased the expression of Grb2 mRNA by 4.8 fold in hepatic cancer cell HepG2. In the present study, we found that NOR1 increased the Grb2 protein expression by 3 fold and enhanced the CB1954 induced cell killing in HepG2 cells ,and the cell cytotoxicity could be inhibited by adding tyrosine kinase inhibitor genestein or by stable transfection of Grb2 shRNA (pU6+27-shGrb2) to silence the expression of Grb2. Western blot analysis showed that Grb2 downexpression could reduce the activity of MAPK. Moreover, inhibiting the activatiton of MAPK by MEK inhibtor PD98059 suppressed CB1954 induced cell killing. These results suggested that NOR1 gene enhanced CB1954 cell cytotoxicity through upregulating expression of Grb2 and activiation of MAPK signal transduction in HepG2 cells.
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