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Myxoid liposarcoma FUS-DDIT3 fusion oncogene induces C/EBP β-mediated interleukin 6 expression
被引:38
作者:
Göransson, M
Elias, E
Ståhlberg, A
Olofsson, A
Andersson, C
Åman, P
机构:
[1] Gothenburg Univ, Lundberg Lab Canc Res, Dept Pathol, S-41345 Gothenburg, Sweden
[2] Chalmers Univ Technol, Dept Chem & Biosci, S-41296 Gothenburg, Sweden
[3] TATAA Bioctr, S-41296 Gothenburg, Sweden
关键词:
MLS/RCLS;
FUS;
DDIT3;
CEBP beta;
NF kappa B;
D O I:
10.1002/ijc.20893
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 [肿瘤学];
摘要:
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 NF kappa B 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 P and NF kappa B. (c) 2005 Wiley-Liss, Inc.
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页码:556 / 560
页数:5
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