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黏液样脂肪肉瘤FUS-DDIT3融合癌基因诱导C/EBPβ介导的白细胞介素6表达。

Myxoid liposarcoma FUS-DDIT3 fusion oncogene induces C/EBP beta-mediated interleukin 6 expression.

作者信息

Göransson Melker, Elias Erik, Ståhlberg Anders, Olofsson Anita, Andersson Carola, Aman Pierre

机构信息

Lundberg Laboratory for Cancer Research (LLCR), Department of Pathology, Goteborg University, Gothenburg, Sweden.

出版信息

Int J Cancer. 2005 Jul 1;115(4):556-60. doi: 10.1002/ijc.20893.

Abstract

The myxoid/round cell liposarcoma oncogene FUS-DDIT3 is the result of a translocation derived gene fusion between the splicing factor FUS and DDIT3. In order to investigate the downstream targets of DDIT3, and the transforming effects of the FUS-DDIT3 fusion protein, we have introduced DDIT3-GFP and FUS-DDIT3-GFP constructs into a human fibrosarcoma cell line. The gene expression profiles of stable transfectants were compared to the original fibrosarcoma cell line by microarray analysis. We here report that the NFkappaB and C/EBP beta controlled gene IL6 is upregulated in DDIT3- and FUS-DDIT3-expressing fibrosarcoma cell lines and in myxoid liposarcoma cell lines. Strong expression of the tumor associated multifunctional cytokine interleukin 6 was confirmed both at mRNA and protein level. Knockdown experiments using siRNA against CEBPB transcripts showed that the effect of FUS-DDIT3 on IL6 expression is C/EBP beta dependent. Chromatin immunoprecipitation revealed direct interaction between the IL6 promoter and the C/EBP beta protein. In addition, the effect of DDIT3 and FUS-DDIT3 on the expression of other acute phase genes was examined using real-time PCR. We demonstrate for the first time that DDIT3 and FUS-DDIT3 show opposite transcriptional regulation of IL8 and suggest that FUS-DDIT3 may affect the synergistic activation of promoters regulated by C/EBP beta and NFkappaB.

摘要

黏液样/圆形细胞脂肪肉瘤致癌基因FUS-DDIT3是剪接因子FUS与DDIT3之间易位衍生的基因融合产物。为了研究DDIT3的下游靶点以及FUS-DDIT3融合蛋白的转化作用,我们将DDIT3-GFP和FUS-DDIT3-GFP构建体导入人纤维肉瘤细胞系。通过微阵列分析将稳定转染子的基因表达谱与原始纤维肉瘤细胞系进行比较。我们在此报告,在表达DDIT3和FUS-DDIT3的纤维肉瘤细胞系以及黏液样脂肪肉瘤细胞系中,NFκB和C/EBPβ调控的基因IL6上调。在mRNA和蛋白水平均证实了肿瘤相关多功能细胞因子白细胞介素6的强表达。使用针对CEBPB转录本的siRNA进行的敲低实验表明,FUS-DDIT3对IL6表达的影响依赖于C/EBPβ。染色质免疫沉淀揭示了IL6启动子与C/EBPβ蛋白之间的直接相互作用。此外,使用实时PCR检测了DDIT3和FUS-DDIT3对其他急性期基因表达的影响。我们首次证明DDIT3和FUS-DDIT3对IL8表现出相反的转录调控,并表明FUS-DDIT3可能影响由C/EBPβ和NFκB调控的启动子的协同激活。

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