Haematologica · 2012 · 71 citations · 13 references
MedicineOncologyPharmacologyApoptosisCell ProliferationMolecular OncologyApoptosis In CancerApoptosis ResistanceGene Fusions In CancerMyeloproliferative NeoplasmsOncogenic ProliferationApoptosis TargetingFgfr Fusion GenesMyeloproliferative Neoplasm TherapyMyeloproliferative Neoplasm TreatmentOncogenic Fusion ProteinsPrimary CellsTherapeutic Targeting Of Fusion ProteinsTranslocations
The 8p11 myeloproliferative syndrome is a rare, aggressive myeloproliferative neoplasm characterized by constitutively active FGFR1 fusion proteins that arise from specific chromosomal translocations and which drive aberrant proliferation. Although FGFR1 inhibitors have shown in vitro activity against FGFR1 fusions, none are in use clinically and there is a need to assess additional compounds as potential therapy. Here we use cell lines and primary cells to investigate ponatinib (AP24534). Ponatinib-treated Ba/F3 cells transformed by ZMYM2-FGFR1 and BCR-FGFR1 and the FGFR1OP2-FGFR1 positive KG1A cell line showed reduced proliferation and decreased survival when compared to control cells. Inhibition induced apoptosis and reduced phosphorylation of the FGFR1 fusion proteins and substrates. Ponatinib-treated cells from 8p11 myeloproliferative syndrome patients (n=5) showed reduced colony growth compared to controls. In one evaluable patient, ponatinib specifically reduced numbers of FGFR1-fusion gene positive colonies. Ponatinib, therefore, shows considerable promise for the treatment of patients with 8p11 myeloproliferative syndrome.
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Jing Chen, Daniel J. DeAngelo, Jeffery L. Kutok et al. · Proceedings of the National Academy of Sciences · 2004 · 172 citations
Medicine, Oncology, Pharmacology +17