1. Activity of the multikinase inhibitor dasatinib against ovarian cancer cells
- Author
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Konecny, GE, Glas, R, Dering, J, Manivong, K, Qi, J, Finn, RS, Yang, GR, Hong, K-L, Ginther, C, Winterhoff, B, Gao, G, Brugge, J, and Slamon, DJ
- Subjects
Ovarian Cancer ,Rare Diseases ,Cancer ,Orphan Drug ,5.1 Pharmaceuticals ,Development of treatments and therapeutic interventions ,Antineoplastic Combined Chemotherapy Protocols ,Apoptosis ,Cell Cycle ,Cell Growth Processes ,Cell Line ,Tumor ,Cell Movement ,Dasatinib ,Female ,Flow Cytometry ,Focal Adhesion Kinase 1 ,Gene Expression Profiling ,Humans ,Inhibitory Concentration 50 ,Ovarian Neoplasms ,Phosphorylation ,Protein Kinase Inhibitors ,Proto-Oncogene Proteins c-yes ,Pyrimidines ,Receptor ,EphA2 ,Thiazoles ,src-Family Kinases ,Src ,Eph2A ,FAK ,uPA ,dasatinib ,ovarian cancer ,Oncology and Carcinogenesis ,Public Health and Health Services ,Oncology & Carcinogenesis - Abstract
BackgroundHere, we explore the therapeutic potential of dasatinib, a small-molecule inhibitor that targets multiple cytosolic and membrane-bound tyrosine kinases, including members of the Src kinase family, EphA2, and focal adhesion kinase for the treatment of ovarian cancer.MethodsWe examined the effects of dasatinib on proliferation, invasion, apoptosis, cell-cycle arrest, and kinase activity using a panel of 34 established human ovarian cancer cell lines. Molecular markers for response prediction were studied using gene expression profiling. Multiple drug effect/combination index (CI) isobologram analysis was used to study the interactions with chemotherapeutic drugs.ResultsConcentration-dependent anti-proliferative effects of dasatinib were seen in all ovarian cancer cell lines tested, but varied significantly between individual cell lines with up to a 3 log-fold difference in the IC(50) values (IC(50) range: 0.001-11.3 micromol l(-1)). Dasatinib significantly inhibited invasion, and induced cell apoptosis, but less cell-cycle arrest. At a wide range of clinically achievable drug concentrations, additive and synergistic interactions were observed for dasatinib plus carboplatin (mean CI values, range: 0.73-1.11) or paclitaxel (mean CI values, range: 0.76-1.05). In this study, 24 out of 34 (71%) representative ovarian cancer cell lines were highly sensitive to dasatinib, compared with only 8 out of 39 (21%) representative breast cancer cell lines previously reported. Cell lines with high expression of Yes, Lyn, Eph2A, caveolin-1 and 2, moesin, annexin-1, and uPA were particularly sensitive to dasatinib.ConclusionsThese data provide a clear biological rationale to test dasatinib as a single agent or in combination with chemotherapy in patients with ovarian cancer.
- Published
- 2009