Monitoring vascular normalization induced by antiangiogenic treatment with (18)F-fluoromisonidazole-PET.
Journal:
Molecular oncology
PMID:
26778791
Abstract
BACKGROUND: Rationalization of antiangiogenics requires biomarkers. Vascular re-normalization is one widely accepted mechanism of action for this drug class. The interstitium of tumors with abnormal vasculature is hypoxic. We sought to track vascular normalization with (18)F-misonidazole ([18F]-FMISO, a probe that detects hypoxia) PET, in response to window-of-opportunity (WoO) treatment with the antiangiogenic dovitinib.
Authors
Keywords
Angiogenesis Inhibitors
Animals
Antimetabolites, Antineoplastic
Benzimidazoles
Breast
Breast Neoplasms
Cell Hypoxia
Cell Line, Tumor
Deoxycytidine
Female
Fluorine Radioisotopes
Gemcitabine
Humans
Mice
Mice, Nude
Misonidazole
Neovascularization, Pathologic
Pancreas
Pancreatic Neoplasms
Positron-Emission Tomography
Quinolones