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Mol Med Rep ; 5(2): 326-30, 2012 02.
Article in English | MEDLINE | ID: mdl-22052253

ABSTRACT

Osteosarcoma (OS) is the most common primary malignant neoplasm in children and adolescents. Epirubicin is one of the chemotherapeutic agents currently used for the treatment of OS; however, the efficacy of chemotherapy is hampered by the acquired drug resistance of OS. Cerulenin, an inhibitor of fatty acid synthase, has been defined as a candidate tumor suppressor. In this study, we explored the combined effect of cerulenin plus the chemotherapy drug, epirubicin, on human OS U2-OS cells in vitro and in vivo. We demonstrated that cerulenin plus epirubicin induced synergistic growth inhibition and enhanced apoptosis in U2-OS cells. We also demonstrated that cerulenin plus epirubicin synergistically suppressed tumor growth in subcutaneously xenografted U2-OS cells in athymic nude mice. Our results indicate that cerulenin enhances the anti-OS effects of epirubicin in vivo and in vitro.


Subject(s)
Antibiotics, Antineoplastic/pharmacology , Antibiotics, Antineoplastic/therapeutic use , Apoptosis/drug effects , Bone Neoplasms/drug therapy , Cerulenin/therapeutic use , Epirubicin/therapeutic use , Osteosarcoma/drug therapy , Animals , Cell Line, Tumor , Cerulenin/pharmacology , Drug Synergism , Epirubicin/pharmacology , Fatty Acid Synthases/antagonists & inhibitors , Fatty Acid Synthases/metabolism , Male , Mice , Mice, Nude , Transplantation, Heterologous
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