British Journal of Cancer · 2005 · 18 citations · 7 references
MedicineOncologyPharmacologyChemotherapyMetastasisMolecular OncologyAngiogenesisAngiogenesis In CancerTargeted Cancer TherapyTargeted TherapyTherapeutic Monoclonal AntibodiesTyrosine Kinase InhibitorsAnticancer ActivityAnticancer ChemotherapyMolecularly Targeted AgentsMonoclonal Antibodies In CancerSmall Molecule Tyrosine Kinase InhibitorsTargeted Molecular TherapyVascular Endothelial Growth Factor InhibitionVascular Endothelial Growth Factor Inhibitors
Better understanding of the pathways regulating proliferation and metastasis of cancer cells has led to the development of novel molecular-targeted therapies. The number of molecular-targeted agents approved for use in the clinic is growing, with many more in clinical trials. Most of these compounds can be broadly classified into two main categories: monoclonal antibodies and small-molecule tyrosine kinase inhibitors. The pathological processes targeted include vascular endothelial growth factor-dependent tumour angiogenesis and epidermal growth factor receptor-dependent tumour cell proliferation and survival. Unlike conventional chemotherapy, molecular-targeted agents offer the potential advantages of a relatively high therapeutic window and use in combination with other anticancer strategies without overlapping toxicity. It is hoped that these drugs will become valuable therapeutic tools within the multimodal approach to treating cancer. Recent progress in targeted antitumour therapy is discussed, with a focus on antiangiogenesis.
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Vascular endothelial growth factor induced by hypoxia may mediate hypoxia-initiated angiogenesis
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