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Cell Rep ; 28(9): 2317-2330.e8, 2019 08 27.
Article in English | MEDLINE | ID: mdl-31461649

ABSTRACT

Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) is a tumor suppressor and bi-functional lipid and protein phosphatase. We report that the metabolic regulator pyruvate dehydrogenase kinase1 (PDHK1) is a synthetic-essential gene in PTEN-deficient cancer and normal cells. The PTEN protein phosphatase dephosphorylates nuclear factor κB (NF-κB)-activating protein (NKAP) and limits NFκB activation to suppress expression of PDHK1, a NF-κB target gene. Loss of the PTEN protein phosphatase upregulates PDHK1 to induce aerobic glycolysis and PDHK1 cellular dependence. PTEN-deficient human tumors harbor increased PDHK1, a biomarker of decreased patient survival. This study uncovers a PTEN-regulated signaling pathway and reveals PDHK1 as a potential target in PTEN-deficient cancers.


Subject(s)
Neoplasms/metabolism , PTEN Phosphohydrolase/genetics , Pyruvate Dehydrogenase Acetyl-Transferring Kinase/genetics , Animals , Cell Line, Tumor , Female , Glycolysis , HEK293 Cells , Humans , Male , Mice , Mice, Inbred NOD , Mice, SCID , NF-kappa B/metabolism , Neoplasms/genetics , Neoplasms/pathology , PTEN Phosphohydrolase/economics , PTEN Phosphohydrolase/metabolism , Pyruvate Dehydrogenase Acetyl-Transferring Kinase/metabolism , Repressor Proteins/metabolism
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