Journal
AMERICAN JOURNAL OF PATHOLOGY
Volume 176, Issue 4, Pages 1941-1949Publisher
AMER SOC INVESTIGATIVE PATHOLOGY, INC
DOI: 10.2353/ajpath.2010.090804
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Funding
- Marshall Program of the Walloon Region [616476]
- Belgian Fund for Medical Scientific Research
- Centre Anti-Cancereux pres l'Universite de Liege
- Faculty of Medicine of the University of Liege
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TP63 is a p53-related gene that contains two alternative promoters which give rise to transcripts that encode proteins with (TAp63) or without (Delta Np63) an amino-transactivating domain. Whereas the expression of p63 is required for proper development of epithelial structures, the role of p63 in tumorigenesis remains unclear. Here, we investigated the role of Snail and Slug transcription factors, known to promote epithelial-to-mesenchymal transitions during development and cancer, in the regulation of p63 isoforms in human squamous cell carcinoma (SCC). In the present study, we observed that the expressions of AN and TAp63 isoforms were, respectively, down- and up-regulated by both Snail and Slug. However, the induction of TAp63 was not directly caused by these two transcription factors but resulted from the loss of Delta Np63, which acts as dominant-negative inhibitor of TAp63. In SCC cell lines and cancer tissues, high expression of Snail and Slug was also significantly associated with altered p63 expression. Finally, we showed that Delta Np63 silencing reduced cell-cell adhesion and increased the migratory properties of cancer cells. These data suggest that the disruption of p63 expression induced by Snail and Slug plays a crucial role in tumor progression. Therefore, p63 and its regulating factors could constitute novel prognosis markers in patients with SCC and attractive targets for the therapeutic modulation of neoplastic cell invasiveness. (Am J Pathol 2010, 176:1941-1949; DOI: 10.2353/ajpath.2010.090804)
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