Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2578999 | Thérapie | 2012 | 13 Pages |
Abstract
Research on molecular alteration process mechanisms leading to cancerogenesis permitted the elaboration of many targeted therapies. Some therapeutic classes appeared recently and are currently being tested, including HER-2 dimerization inhibitors. However, most of these therapies are mostly ineffective with monotherapy. Clinical trials are ongoing, testing their efficiency in association with other molecules of the therapeutic arsenal which is available in oncology. Nevertheless, breast cancer remains a pathology life-threatening, most of the time. Within this review will be introduced the most efficient of these targeted therapies, including their eventual association with other cytotoxic molecules.
Keywords
ADCCm-TORBRCA-1AMMGRB2IGFR1ITKT-DM1HER-2RADPDGFSOSBcrpPARPERK2ERK1RASHSP90PI3KAktHERImmunohistochimieIHCTAMTyrosine kinaseThérapie cibléeTargeted therapytenrat sarcomacancer du sein métastatiqueHuman epidermal growth factorVascular endothelial growth factorVascular Endothelial Growth Factor (VEGF)platelet-derived growth factorphosphatase and tensin homologPhosphorylationphosphoinositide 3-kinasefluorescence in situ hybridizationFishMEKautorisation de mise sur le marchéétude cliniqueinhibiteur de tyrosine kinaseMammalian target of rapamycin inhibitorsChromogenic in situ hybridizationbreast cancer resistance proteingrowth factor receptor-bound protein 2son of sevenlessClinical trialCISHHuman epidermal growth factor receptor-2
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Authors
Laure Belmondo, Marc Montana, Christophe Curti, Maxime Crozet, Pascal Rathelot, Christine Penot-Ragon, Patrice Vanelle,