| Literature DB >> 12489109 |
Hugo Leis1, Carmen Segrelles, Sergio Ruiz, Mirentxu Santos, Jesús M Paramio.
Abstract
Glycogen synthase kinase 3 (GSK-3) is a protein kinase that plays essential roles in the control of several developmental, metabolic, and apoptotic processes. Owing to its negative actions on several oncogenic insults, it has been considered a putative functional tumor suppressor. We studied the expression, activity, and localization of GSK-3beta during the process of chemically induced two-stage mouse skin carcinogenesis and also in the tumors generated upon subcutaneous injection of Akt-transformed keratinocytes. We found that GSK-3 activity was downregulated at the later stages of promotion by tyrosine 216 dephosphorylation and serine 9 phosphorylation. The data obtained with Akt-transformed keratinocytes clearly suggested the involvement of Akt in serine 9 phosphorylation of GSK-3beta. Finally, besides functional inactivation, significant basal activity of GSK-3beta was detected in all cases, indicating that this enzyme provides essential functions to malignant keratinocytes. Copyright 2002 Wiley-Liss, Inc.Entities:
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Year: 2002 PMID: 12489109 DOI: 10.1002/mc.10087
Source DB: PubMed Journal: Mol Carcinog ISSN: 0899-1987 Impact factor: 4.784