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Publication : Reactivation of developmentally expressed p63 isoforms predisposes to tumor development and progression.

First Author  Koster MI Year  2006
Journal  Cancer Res Volume  66
Issue  8 Pages  3981-6
PubMed ID  16618715 Mgi Jnum  J:108308
Mgi Id  MGI:3623671 Doi  10.1158/0008-5472.CAN-06-0027
Citation  Koster MI, et al. (2006) Reactivation of developmentally expressed p63 isoforms predisposes to tumor development and progression. Cancer Res 66(8):3981-6
abstractText  Genes that are active during normal development are frequently reactivated during neoplastic transformation. We now report that developmentally expressed TAp63 isoforms are frequently reactivated in human squamous cell carcinomas. To determine the consequences of TAp63 reactivation, we induced TAp63alpha expression during chemically-induced skin carcinogenesis. Deregulated TAp63alpha expression dramatically accelerated tumor development and progression, frequently resulting in epithelial-mesenchymal transitions to spindle cell carcinomas and lung metastases. Consistent with this observation, we detected high levels of Twist and N-cadherin in tumors overexpressing TAp63alpha. Thus, as observed for other developmental pathways, aberrant reactivation of TAp63 predisposes to tumor development and progression.
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