Identification of IGFBP-6 as a significantly downregulated gene by β-catenin in desmoid tumors

被引:33
作者
Denys, H
Jadidizadeh, A
Nik, SA
Van Dam, K
Aerts, S
Alman, BA
Cassiman, JJ
Tejpar, S
机构
[1] Catholic Univ Louvain, Ctr Human Genet, B-3000 Louvain, Belgium
[2] Univ Louvain, Dept Elect Engn, B-3001 Heverlee, Belgium
[3] Hosp Sick Children, Program Dev Biol, Toronto, ON M5G 1X8, Canada
[4] Univ Toronto, Toronto, ON M5G 1X8, Canada
关键词
beta-catenin; IGFBP-6; expression profile; desmoid; target genes;
D O I
10.1038/sj.onc.1207160
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Desmoid tumors (aggressive fibromatosis) are locally invasive soft tissue tumors in which beta-catenin-mediated TCF-3-dependent transcription is activated. To provide more insight into the pathophysiology of these tumors, expression profiles were generated using oligonucleotide arrays (Affymetrix). In total, 69 differentially expressed genes were identified in desmoids compared to normal fibroblasts (fascia) from the same patients. The differential expression of a selection of genes was confirmed using RT-PCR and Northern blotting. We further evaluated the insulin-like growth factor-binding protein 6 (IGFBP-6), a gene that was consistently downregulated in all desmoids tested. Promotor studies and electromobility shift assays revealed two functional beta-catenin/TCF-responsive elements in the human IGFBP-6 promoter. These findings suggest that IGFBP-6 is directly downregulated by the beta-catenin/TCF complex in desmoid tumors, and imply a role for the IGF axis in the proliferation of desmoid tumors.
引用
收藏
页码:654 / 664
页数:11
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