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Targeted deletion of Wwox reveals a tumor suppressor function.

ABSTRACT: The WW domain-containing oxidoreductase (WWOX) spans the second most common fragile site of the human genome, FRA16D, located at 16q23, and its expression is altered in several types of human cancer. We have previously shown that restoration of WWOX expression in cancer cells suppresses tumorigenicity. To investigate WWOX tumor suppressor function in vivo, we generated mice carrying a targeted deletion of the Wwox gene and monitored incidence of tumor formation. Osteosarcomas in juvenile Wwox(-/-) and lung papillary carcinoma in adult Wwox(+/-) mice occurred spontaneously. In addition, Wwox(+/-) mice develop significantly more ethyl nitrosourea-induced lung tumors and lymphomas in comparison to wild-type littermate mice. Intriguingly, these tumors still express Wwox protein, suggesting haploinsuffiency of WWOX itself is cancer predisposing. These results indicate that WWOX is a bona fide tumor suppressor.

SUBMITTER: Aqeilan RI 

PROVIDER: S-EPMC1820689 | biostudies-literature | 2007 Mar

REPOSITORIES: biostudies-literature

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Targeted deletion of Wwox reveals a tumor suppressor function.

Aqeilan Rami I RI   Trapasso Francesco F   Hussain Sadiq S   Costinean Stefan S   Marshall Dean D   Pekarsky Yuri Y   Hagan John P JP   Zanesi Nicola N   Kaou Mohamed M   Stein Gary S GS   Lian Jane B JB   Croce Carlo M CM  

Proceedings of the National Academy of Sciences of the United States of America 20070227 10

The WW domain-containing oxidoreductase (WWOX) spans the second most common fragile site of the human genome, FRA16D, located at 16q23, and its expression is altered in several types of human cancer. We have previously shown that restoration of WWOX expression in cancer cells suppresses tumorigenicity. To investigate WWOX tumor suppressor function in vivo, we generated mice carrying a targeted deletion of the Wwox gene and monitored incidence of tumor formation. Osteosarcomas in juvenile Wwox(-/  ...[more]

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