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Nat Med ; 10(3): 262-7, 2004 Mar.
Article in English | MEDLINE | ID: mdl-14981513

ABSTRACT

The Aurora kinases are essential for the regulation of chromosome segregation and cytokinesis during mitosis. Aberrant expression and activity of these kinases occur in a wide range of human tumors, and lead to aneuploidy and tumorigenesis. Here we report the discovery of a highly potent and selective small-molecule inhibitor of Aurora kinases, VX-680, that blocks cell-cycle progression and induces apoptosis in a diverse range of human tumor types. This compound causes profound inhibition of tumor growth in a variety of in vivo xenograft models, leading to regression of leukemia, colon and pancreatic tumors at well-tolerated doses. Our data indicate that Aurora kinase inhibition provides a new approach for the treatment of multiple human malignancies.


Subject(s)
Enzyme Inhibitors/metabolism , Enzyme Inhibitors/therapeutic use , Neoplasms/drug therapy , Neoplasms/metabolism , Piperazines/therapeutic use , Protein Serine-Threonine Kinases/antagonists & inhibitors , Animals , Apoptosis/physiology , Aurora Kinases , Cell Cycle/physiology , Cell Line, Tumor , Enzyme Inhibitors/chemistry , Female , Histones/metabolism , Humans , Mice , Mice, Nude , Molecular Structure , Piperazines/chemistry , Piperazines/pharmacology , Protein Serine-Threonine Kinases/metabolism , Rats
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