Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10872178 | FEBS Letters | 2009 | 7 Pages |
Abstract
The complexity of the mammalian p53 pathway and protein kinase C (PKC) family has hampered the discrimination of the effect of PKC isoforms on p53 activity. Using yeasts co-expressing the human wild-type p53 and a mammalian PKC-α, -δ, -ε or -ζ, we showed a differential regulation of p53 activity and phosphorylation state by PKC isoforms. Whereas PKC-α reduced the p53-induced yeast growth inhibition and cell cycle arrest, PKC-δ and -ε enhanced the p53 activity through p53 phosphorylation, and PKC-ζ had no effect on p53. This work identified positive and negative p53 regulators which represent promising pharmacological targets in anti-cancer therapy.
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Authors
Isabel Coutinho, Gil Pereira, Mariana Leão, Jorge Gonçalves, Manuela Côrte-Real, LucÃlia Saraiva,