Journal article
Mutant p53 oncogenic functions are sustained by Plk2 kinase through an autoregulatory feedback loop
Abstract
Aberrant activation of kinases has emerged to be a key event along with tumor progression, maintenance of tumor phenotype and response to anticancer treatments. This study documents the existence of an oncogenic auto-regulatory feedback loop that includes the Polo-like kinase-2 (Snk/Plk2) and mutant p53 proteins. Plk2 protein binds to and phosphorylates mutant p53, thereby potentiating its oncogenic activities. Phosphorylated mutant p53 binds …
Authors
Valenti F; Fausti F; Biagioni F; Shay T; Fontemaggi G; Domany E; Yaffe MB; Strano S; Blandino G; Di Agostino S
Journal
Cell Cycle, Vol. 10, No. 24, pp. 4330–4340
Publisher
Taylor & Francis
Publication Date
December 15, 2011
DOI
10.4161/cc.10.24.18682
ISSN
1538-4101
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Cell Line, TumorChromatin ImmunoprecipitationDNA DamageDNA PrimersE1A-Associated p300 ProteinElectrophoresis, Polyacrylamide GelFeedback, PhysiologicalGene Expression Regulation, NeoplasticHumansImmunoprecipitationNeoplasmsPhosphorylationProtein Serine-Threonine KinasesRNA InterferenceRNA, Small InterferingReal-Time Polymerase Chain ReactionTransfectionTumor Suppressor Protein p53