CDX2 promotes anchorage-independent growth bytranscriptional repression of IGFBP-3

被引:20
作者
Chun, S. Y.
Chen, F.
Washburn, J. G.
MacDonald, J. W.
Innes, K. L.
Zhao, R.
Cruz-Correa, M. R.
Dang, L. H.
Dang, D. T.
机构
[1] Univ Michigan, Dept Internal Med, Div Gastroenterol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Internal Med, Div Hematol Oncol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Ctr Comprehens Canc, Affymetrix & cDNA Microarray Core Facil, Ann Arbor, MI 48109 USA
[4] Univ Puerto Rico, Ctr Comprehens Canc, Dept Internal Med, Div Gastroenterol, San Juan, PR 00936 USA
关键词
CDX2; IGFBP-3; colorectal cancer; anchorageindependent growth;
D O I
10.1038/sj.onc.1210258
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
CDX2 is a Drosophila caudal-related homeobox transcription factor that is important for the establishment and maintenance of intestinal epithelial cells. We have reported that CDX2 promotes tumorigenicity in a subset of human colorectal cancer cell lines. Here, we present evidence that CDX2 negatively regulates the well-documented growth inhibitor insulin-like growth factor binding protein-3 IGFBP-3). Specifically, CDX2 binds to the IGFBP-3 gene promoter and can repress IGFBP-3 transcription, protein expression and secretion. Furthermore, inhibition of IGFBP-3 partially rescues the decreased anchorage-independent growth phenotype observed in CDX2 knockout cells. These data demonstrate for the first time that (1) CDX2 can function as a transcriptional repressor, and ( 2) one mechanism by which CDX2 promotes anchorage-independent growth is by transcriptional repression of IGFBP-3.
引用
收藏
页码:4725 / 4729
页数:5
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