Titlebook: Antiangiogenic Agents in Cancer Therapy; Beverly A. Teicher,Lee M. Ellis Book 2008Latest edition Humana Press 2008 CNS.Chemokine.angiogene

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Robert F. Schmidt,Gerhard Thewsvessels is required. This recognition has led to the development and clinical advancement of novel antiangiogenic therapeutics in cancer management. An alternative approach to targeting the neovasculature associated with tumors is not to interfere with new vessel formation but rather to disrupt the

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Vascular Endothelial Growth Factor Family and Its Receptors vascular growth during physiological and pathological processes in the adult. The VEGF family of ligands in mammals includes VEGF-A, VEGF-B, VEGF-C, VEGF-D, and placenta growth factor (PlGF). These ligands bind to and activate three receptor tyrosine kinases, designated VEGFR-1, VEGFR-2, and VEGFR-

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The Cycle Between Angiogenesis, Perfusion, and Hypoxia in Tumorslated angiogenesis, instability in perfusion, and hypoxia. Interactions between tumor and endothelial cells occur during tumor growth and in response to therapy. These interactions are of central importance in establishing codependence that contributes to promotion of tumor and endothelial cell surv

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Chemokines in Angiogenesisogenesis can occur under physiological conditions that include embryogenesis and the ovarian/menstrual cycle. In contrast, pathological angiogenesis is associated with chronic inflammation/chronic fibroproliferative disorders and tumorigenesis of cancer. Net angiogenesis is determined by a balance i