PubMed · 2010 · 18 citations · 46 references
MedicineOncologyPharmacologyCancer PharmacologyMolecular OncologyOncology PharmacotherapyMalignant NeoplasmsMtor Inhibitor TherapyPharmacodynamics Of Anticancer AgentsPharmacodynamics Of Anticancer DrugsAdditive EffectsAnticancer ActivityAntiproliferative AgentsAntiproliferative Drug ActionCancer Cell Proliferation InhibitionMtor InhibitionMtor SignalingProtein Kinase Inhibitors
BACKGROUND/AIM: Beyond their primary field of application some well-established drugs exhibit antitumour effects in a variety of cancers. The aim of this study was to investigate the effects of the COX2 inhibitor celecoxib and the mTOR antagonist rapamycin on angiosarcoma cell lines. MATERIALS AND METHODS: Cell proliferation was measured in ASM, ISOS 1 and ISO HAS angiosarcoma cell lines with the BrdU assay. RESULTS: In all angiosarcoma cell lines, celecoxib as well as rapamycin inhibited cell growth in a dose-dependent manner. In ASM and ISOS 1, but not in ISO HAS angiosarcoma cells, additive growth inhibitory effects were detected by combining both agents. CONCLUSION: Our results indicate that angiosarcoma cell proliferation can be inhibited by subtoxic doses of rapamycin and celecoxib. Due to their direct and stroma-mediated anticancer activities, mTOR antagonists and COX2 inhibitors represent very promising drugs in the palliative treatment of angiosarcoma.
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Sirolimus for Kaposi's Sarcoma in Renal-Transplant Recipients
Giovanni Stallone, Antonio Schena, Barbara Infante et al. · New England Journal of Medicine · 2005 · 984 citations · Full text
Medicine, Immunology, Nephrology +12