Biological and Pharmaceutical Bulletin · 2009 · 53 citations · 27 references
Pi3k InhibitorsChemoprevention StrategyMolecular BiologyDna-dependent Protein KinaseGliomaTumor BiologyOncologyCell RegulationSignaling PathwayReceptor Tyrosine KinaseAnti-cancer AgentCell SignalingCancer ResearchPharmacologyCell BiologyProtein PhosphorylationSignal TransductionNatural SciencesOther Pi3k InhibitorsTumor SuppressorCellular BiochemistryMedicine
Phosphatidylinositol 3-kinase (PI3K) has been implicated in a variety of diseases including cancer. A number of PI3K inhibitors have recently been developed for use in cancer therapy. ZSTK474 is a highly promising antitumor agent targeting PI3K. We previously reported that ZSTK474 showed potent inhibition against four class I PI3K isoforms but not against 140 protein kinases. However, whether ZSTK474 inhibits DNA-dependent protein kinase (DNA-PK), which is structurally similar to PI3K, remains unknown. To investigate the inhibition of DNA-PK, we developed a new DNA-PK assay method using Kinase-Glo. The inhibition activity of ZSTK474 against DNA-PK was determined, and shown to be far weaker compared with that observed against PI3K. The inhibition selectivity of ZSTK474 for PI3K over DNA-PK was significantly higher than other PI3K inhibitors, namely NVP-BEZ235, PI-103 and LY294002. These results indicated that ZSTK474 was the most specific agent among these PI3K inhibitors.
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High Frequency of Mutations of the <i>PIK3CA</i> Gene in Human Cancers
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