AT7867 is a potent and oral inhibitor of AKT and p70 S6 kinase that induces pharmacodynamic changes and inhibits human tumor xenograft growth
| Autor: | T.G. Davies, Lisa Jane K. Hunter, Michelle D. Garrett, Matthias Reule, Timothy A. Yap, Lisa C A Seavers, Steven John Woodhead, Kyla Grimshaw, Lynsey Fazal, Neil T. Thompson, John Lyons, Paul Workman, Simon P. Heaton, Michael I. Walton, Victoria Lock |
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| Rok vydání: | 2010 |
| Předmět: |
Male
Models Molecular Cancer Research Administration Oral Down-Regulation Mice Nude Antineoplastic Agents Pharmacology Biology Models Biological Article chemistry.chemical_compound Mice Piperidines Cell Line Tumor Neoplasms Animals Humans Protein kinase A Protein kinase B Protein Kinase Inhibitors Cell Proliferation Mice Inbred BALB C Dose-Response Relationship Drug Cell growth Kinase Akt/PKB signaling pathway Ribosomal Protein S6 Kinases 70-kDa HCT116 Cells Xenograft Model Antitumor Assays Oncogene Protein v-akt Treatment Outcome Oncology chemistry Phosphorylation Pyrazoles Signal transduction Growth inhibition HT29 Cells |
| Zdroj: | Molecular cancer therapeutics. 9(5) |
| ISSN: | 1538-8514 |
| Popis: | The serine/threonine kinase AKT plays a pivotal role in signal transduction events involved in malignant transformation and chemoresistance and is an attractive target for the development of cancer therapeutics. Fragment-based lead discovery, combined with structure-based drug design, has recently identified AT7867 as a novel and potent inhibitor of both AKT and the downstream kinase p70 S6 kinase (p70S6K) and also of protein kinase A. This ATP-competitive small molecule potently inhibits both AKT and p70S6K activity at the cellular level, as measured by inhibition of GSK3β and S6 ribosomal protein phosphorylation, and also causes growth inhibition in a range of human cancer cell lines as a single agent. Induction of apoptosis was detected by multiple methods in tumor cells following AT7867 treatment. Administration of AT7867 (90 mg/kg p.o. or 20 mg/kg i.p.) to athymic mice implanted with the PTEN-deficient U87MG human glioblastoma xenograft model caused inhibition of phosphorylation of downstream substrates of both AKT and p70S6K and induction of apoptosis, confirming the observations made in vitro. These doses of AT7867 also resulted in inhibition of human tumor growth in PTEN-deficient xenograft models. These data suggest that the novel strategy of AKT and p70S6K blockade may have therapeutic value and supports further evaluation of AT7867 as a single-agent anticancer strategy. Mol Cancer Ther; 9(5); 1100–10. ©2010 AACR. |
| Databáze: | OpenAIRE |
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