The publication detail shows the title, authors (with indicators showing other profiled authors), information on the publishing organization, abstract and a link to the article in PubMed. This abstract is what is used to create the fingerprint of the publication. If any grants are referenced by the publication, they will be listed here as well.
DeltaNp63 induces beta-catenin nuclear accumulation and signaling.
Meera Patturajan; Shuji Nomoto; Matthias Sommer; Alexey Fomenkov; Kenji Hibi; Rachel Zangen; Nina Poliak; Joseph Califano; Barry Trink; Edward Ratovitski; et al. (Profiled Authors: Edward Ratovitski; Barry Trink; Joseph Califano; David Sidransky)
Department of Otolaryngology-Head and Neck Surgery, John Hopkins School of Medicine, Baltimore, MD 21205, USA.
Cancer cell 2002;1(4):369-79.
The P53 homolog p63 encodes multiple proteins with transactivating, apoptosis-inducing, and oncogenic activities. We showed that p63 is amplified and that DeltaNp63 isotypes are overexpressed in squamous cell carcinoma (SCC) and enhance oncogenic growth in vitro and in vivo. Moreover, p53 associated with DeltaNp63alpha and mediated its degradation. Here, we report that DeltaNp63 associates with the B56alpha regulatory subunit of protein phosphatase 2A (PP2A) and glycogen synthase kinase 3beta (GSK3beta), leading to a dramatic inhibition of PP2A-mediated GSK3beta reactivation. The inhibitory effect of DeltaNp63 on GSK3beta mediates a decrease in phosphorylation levels of beta-catenin, which induces intranuclear accumulation of beta-catenin and activates beta-catenin-dependent transcription. Our results suggest that DeltaNp63 isotypes act as positive regulators of the beta-catenin signaling pathway, providing a basis for their oncogenic properties.
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