Plk1 phosphorylation of PTEN causes a tumor-promoting metabolic state.

One outcome of activation of the phosphatidylinositol 3-kinase (PI3K) pathway is increased aerobic glycolysis, but the upstream signaling events that regulate the PI3K pathway, and thus the Warburg effect, are elusive. Increasing evidence suggests that Plk1, a cell cycle regulator, is also involved in cellular events in addition to mitosis. ...
To test whether Plk1 contributes to activation of the PI3K pathway, and thus aerobic glycolysis, we examined potential targets of Plk1 and identified PTEN as a Plk1 substrate. We hypothesize that Plk1 phosphorylation of PTEN leads to its inactivation, activation of the PI3K pathway, and the Warburg effect. Our data show that overexpression of Plk1 leads to activation of the PI3K pathway and enhanced aerobic glycolysis. In contrast, inhibition of Plk1 causes markedly reduced glucose metabolism in mice. Mechanistically, we show that Plk1 phosphorylation of PTEN and Nedd4-1, an E3 ubiquitin ligase of PTEN, results in PTEN inactivation. Finally, we show that Plk1 phosphorylation of PTEN promotes tumorigenesis in both its phosphatase-dependent and -independent pathways, revealing potentially new drug targets to arrest tumor cell growth.
Mesh Terms:
Animals, Antineoplastic Agents, Benzamides, Cell Cycle Proteins, Cell Line, Tumor, Cell Transformation, Neoplastic, Endosomal Sorting Complexes Required for Transport, Gene Expression Regulation, Glucose, Glycolysis, HEK293 Cells, Heterocyclic Compounds, 2-Ring, Humans, Lactic Acid, Liver, Mice, Mice, Nude, Neoplasms, Experimental, Nocodazole, PTEN Phosphohydrolase, Phosphatidylinositol 3-Kinase, Phosphorylation, Protein-Serine-Threonine Kinases, Proto-Oncogene Proteins, Pteridines, Signal Transduction, Ubiquitin-Protein Ligases
Mol. Cell. Biol.
Date: Oct. 01, 2014
Download Curated Data For This Publication
198741
Switch View:
  • Interactions 5