Inhibition of the Wnt/β-catenin pathway by the WWOX tumor suppressor protein

被引:89
作者
Bouteille, N. [2 ]
Driouch, K. [2 ]
El Hage, P. [2 ]
Sin, S. [2 ]
Formstecher, E. [3 ]
Camonis, J. [4 ]
Lidereau, R. [2 ]
Lallemand, F. [1 ,2 ]
机构
[1] Ctr Rene Huguenin, Serv Oncogenet, INSERM, U528,FNCLCC, F-92210 St Cloud, France
[2] INSERM, U735, St Cloud, France
[3] Hybrigenics, Paris, France
[4] Inst Curie, INSERM, U528, Paris 05, France
关键词
WWOX; dishevelled; Wnt; beta-catenin; signaling pathway; CHROMOSOMAL FRAGILE SITE; WNT SIGNALING PATHWAY; KINASE-I-EPSILON; CANCER CELL-GROWTH; BREAST-CANCER; BETA-CATENIN; BINDING PROTEIN; GENE WWOX; C-JUN; EXPRESSION;
D O I
10.1038/onc.2009.120
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
The WWOX gene encodes a candidate tumor suppressor protein (WWOX) implicated in a variety of human diseases such as cancer. To better understand the molecular mechanisms of WWOX action, we investigated novel partners of this protein. Using the two-hybrid system and a coimmunoprecipitation assay, we observed a physical association between WWOX and the Dishevelled protein (Dvl) family signaling elements involved in the Wnt/beta-catenin pathway. We found that enforced WWOX expression inhibited, and inhibition of endogenous WWOX expression stimulated the transcriptional activity of the Wnt/beta-catenin pathway. Inhibition of endogenous WWOX expression also enhanced the effect of Wnt-3a on beta-catenin stability. Moreover, we observed the sequestration of Dvl-2 wild type and Dvl-2NESm, a mutated form of Dvl-2 predominantly localized in the nucleus, in the cytoplasm compartment by WWOX. Our results indicate that WWOX is a novel inhibitor of the Wnt/beta-catenin pathway. WWOX would act, at least in part, by preventing the nuclear import of the Dvl proteins. Oncogene (2009) 28, 2569-2580; doi: 10.1038/onc.2009.120; published online 25 May 2009
引用
收藏
页码:2569 / 2580
页数:12
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