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.
引用
收藏
页码:556 / 560
页数:5
相关论文
共 33 条
[1]
A NUCLEAR FACTOR FOR IL-6 EXPRESSION (NF-IL6) IS A MEMBER OF A C/EBP FAMILY [J].
AKIRA, S ;
ISSHIKI, H ;
SUGITA, T ;
TANABE, O ;
KINOSHITA, S ;
NISHIO, Y ;
NAKAJIMA, T ;
HIRANO, T ;
KISHIMOTO, T .
EMBO JOURNAL, 1990, 9 (06) :1897-1906
[2]
REARRANGEMENT OF THE TRANSCRIPTION FACTOR GENE CHOP IN MYXOID LIPOSARCOMAS WITH T(12 16)(Q13 P11) [J].
AMAN, P ;
RON, D ;
MANDAHL, N ;
FIORETOS, T ;
HEIM, S ;
ARHEDEN, K ;
WILLEN, H ;
RYDHOLM, A ;
MITELMAN, F .
GENES CHROMOSOMES & CANCER, 1992, 5 (04) :278-285
[3]
Analysis of ATF3, a transcription factor induced by physiological stresses and modulated by gadd153/Chop10 [J].
Chen, BPC ;
Wolfgang, CD ;
Hai, TW .
MOLECULAR AND CELLULAR BIOLOGY, 1996, 16 (03) :1157-1168
[4]
FUSION OF CHOP TO A NOVEL RNA-BINDING PROTEIN IN HUMAN MYXOID LIPOSARCOMA [J].
CROZAT, A ;
AMAN, P ;
MANDAHL, N ;
RON, D .
NATURE, 1993, 363 (6430) :640-644
[5]
A LIVER-ENRICHED TRANSCRIPTIONAL ACTIVATOR PROTEIN, LAP, AND A TRANSCRIPTIONAL INHIBITORY PROTEIN, LIP, ARE TRANSLATED FROM THE SAME MESSENGER-RNA [J].
DESCOMBES, P ;
SCHIBLER, U .
CELL, 1991, 67 (03) :569-579
[6]
Analysis of gene function in somatic mammalian cells using small interfering RNAs [J].
Elbashir, SM ;
Harborth, J ;
Weber, K ;
Tuschl, T .
METHODS, 2002, 26 (02) :199-213
[7]
Interleukin-6 is an autocrine growth factor in human prostate cancer [J].
Giri, D ;
Ozen, M ;
Ittmann, M .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 159 (06) :2159-2165
[8]
C/EBP homologous protein (CHOP) up-regulates IL-6 transcription by trapping negative regulating NF-IL6 isoform [J].
Hattori, T ;
Ohoka, N ;
Hayashi, H ;
Onozaki, K .
FEBS LETTERS, 2003, 541 (1-3) :33-39
[9]
AUTOCRINE GENERATION AND REQUIREMENT OF BSF-2/IL-6 FOR HUMAN MULTIPLE MYELOMAS [J].
KAWANO, M ;
HIRANO, T ;
MATSUDA, T ;
TAGA, T ;
HORII, Y ;
IWATO, K ;
ASAOKU, H ;
TANG, B ;
TANABE, O ;
TANAKA, H ;
KURAMOTO, A ;
KISHIMOTO, T .
NATURE, 1988, 332 (6159) :83-85
[10]
THE P50 SUBUNIT OF NF-KAPPA-B ASSOCIATES WITH THE NF-IL6 TRANSCRIPTION FACTOR [J].
LECLAIR, KP ;
BLANAR, MA ;
SHARP, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (17) :8145-8149