| Literature DB >> 15695340 |
Betina Kerstin Lundholt1, Viggo Linde, Frosty Loechel, Hans-Christian Pedersen, Søren Møller, Morten Praestegaard, Ivan Mikkelsen, Kurt Scudder, Sara Petersen Bjørn, Morten Heide, Per O G Arkhammar, Robert Terry, Søren Jensby Nielsen.
Abstract
The PI3-kinase/Akt pathway is an important cell survival pathway that is deregulated in the majority of human cancers. Despite the apparent druggability of several kinases in the pathway, no specific catalytic inhibitors have been reported in the literature. The authors describe the development of a fluorometric imaging plate reader (FLIPR)-based Akt1 translocation assay to discover inhibitors of Akt1 activation. Screening of a diverse chemical library of 45,000 compounds resulted in identification of several classes of Akt1 translocation inhibitors. Using a combination of classical in vitro assays and translocation assays directed at different steps of the Akt pathway, the mechanisms of action of 2 selected chemical classes were further defined. Protein translocation assays emerge as powerful tools for hit identification and characterization.Entities:
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Year: 2005 PMID: 15695340 DOI: 10.1177/1087057104269989
Source DB: PubMed Journal: J Biomol Screen ISSN: 1087-0571