Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/5477
Title: Antiproliferative and proapoptotic activities of new pyrazolo[3,4-d]pyrimidine derivative Src kinase inhibitors in human osteosarcoma cells.
Authors: Spreafico, A
Schenone, S
Serchi, T
Orlandini, Maurizio 
Angelucci, A
Magrini, D
Bernardini, Giulia 
Collodel, Giulia
DI STEFANO, Anna
Tintori, C
Bologna, M
Manetti, Fabrizio 
Botta, Maurizio 
Santucci, Annalisa 
Issue Date: 2008
Project: None 
Journal: THE FASEB JOURNAL
Abstract: 
Osteosarcoma is the most frequent primitive malignant tumor of the skeletal system, characterized by an extremely aggressive clinical course that still lacks an effective treatment. Src kinase seems to be involved in the osteosarcoma malignant phenotype. We show that the treatment of human osteosarcoma cell lines with a new pyrazolo[3,4-d]pyrimidine derivative Src inhibitor, namely SI-83, impaired cell viability, with a half-maximal inhibitory concentration of 12 microM in nonstarved cells and a kinetic different from that known for the Src inhibitor PP2. Analysis by terminal deoxynucleotidyl transferase-mediated nick end labeling, Hoechst, and flow cytometric assay showed that SI-83 induced apoptosis in SaOS-2 cells. Moreover, SI-83, by inhibiting Src phosphorylation, decreased in vivo osteosarcoma tumor mass in a mouse model. Finally, SI-83 showed selectivity for osteosarcoma, since it had a far lower effect in primary human osteoblasts. These results show that human osteosarcoma had Src-dependent proliferation and that modulation of Src activity may be a therapeutic target of this new compound with low toxicity for nonneoplastic cells.
Description: 
35696
URI: http://hdl.handle.net/20.500.12779/5477
ISSN: 0892-6638
DOI: 10.1096/fj.07-9873com
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