Sunitinib treatment does not improve blood supply but induces hypoxia in human melanoma xenografts

• Published in: BMC cancer Vol. 12; no. 1; p. 388
• Main Authors: Gaustad, Jon-Vidar, Simonsen, Trude G, Leinaas, Marit N, Rofstad, Einar K
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 04.09.2012; BioMed Central; BMC
• Subjects: Angiogenesis; Angiogenesis Inhibitors - administration & dosage; Angiogenesis Inhibitors - pharmacology; Animals; Antiangiogenic treatment; Antimitotic agents; Antineoplastic agents; Antineoplastic Agents - administration & dosage; Antineoplastic Agents - pharmacology; Basement Membrane - drug effects; Blood; Blood Vessels - drug effects; Blood Vessels - metabolism; Blood Vessels - pathology; Blood-vessels; Cancer; Care and treatment; Cell growth; Cell Hypoxia; Complications and side effects; Dextran; Dosage and administration; Experiments; Female; Humans; Hypoxia; Indoles - administration & dosage; Indoles - pharmacology; Intravital microscopy; Ionizing radiation; Laboratory animals; Medical research; Melanoma; Melanoma - blood supply; Melanoma - drug therapy; Melanoma - pathology; Mice; Mice, Nude; Neovascularization, Pathologic - drug therapy; Neovascularization, Pathologic - pathology; Patient outcomes; Permeability; Physiological aspects; Pyrroles - administration & dosage; Pyrroles - pharmacology; Rodents; Spheroids, Cellular; Stem cells; Studies; Sunitinib; Tumor Burden - drug effects; Tumor Cells, Cultured; Tumor hypoxia; Tumors; Vascular endothelial growth factor; Vascular normalization; Xenograft Model Antitumor Assays
• ISSN: 1471-2407; 1471-2407
• DOI: 10.1186/1471-2407-12-388

Antiangiogenic agents that disrupt the vascular endothelial growth factor pathway have been demonstrated to normalize tumor vasculature and improve tumor oxygenation in some studies and to induce hypoxia in others. The aim of this preclinical study was to investigate the effect of sunitinib treatment on the morphology and function of tumor vasculature and on tumor oxygenation. A-07-GFP and R-18-GFP human melanoma xenografts grown in dorsal window chambers were used as preclinical tumor models. Morphologic parameters of tumor vascular networks were assessed from high-resolution transillumination images, and tumor blood supply time was assessed from first-pass imaging movies recorded after a bolus of 155 kDa tetramethylrhodamine isothiocyanate-labeled dextran had been administered intravenously. Tumor hypoxia was assessed from immunohistochemical preparations of the imaged tissue by use of pimonidazole as a hypoxia marker. Sunitinib treatment reduced vessel densities, increased vessel segment lengths, did not affect blood supply times, and increased hypoxic area fractions. Sunitinib treatment did not improve vascular function but induced hypoxia in A-07-GFP and R-18-GFP tumors.