Characterisation of tumour vasculature in mouse brain by USPIO contrast-enhanced MRI

Autor: O. van Tellingen, C.N. Maass, A.J. van der Kogel, William P.J. Leenders, Arend Heerschap, Giulio Gambarota, Pieter Wesseling
Rok vydání: 2008
Předmět:
Gadolinium DTPA
Cancer Research
Pathology
Relaxation
Angiogenesis
Melanoma
Experimental

Contrast Media
Vascular permeability
Blood volume
Aetiology
screening and detection [ONCOL 5]

Metastases
Agent
030218 nuclear medicine & medical imaging
Mice
0302 clinical medicine
Gliomas
U87
Magnetite Nanoparticles
Melanoma
Molecular diagnosis
prognosis and monitoring [UMCN 1.2]

Cancer
Blood Volume
medicine.diagnostic_test
Progression
Brain Neoplasms
Dextrans
Oxides
Human brain
Glioma
contrast agent
Magnetic Resonance Imaging
VEGF
Mitochondrial medicine [IGMD 8]
medicine.anatomical_structure
Oncology
mouse brain
Chemical and physical biology [NCMLS 7]
medicine.medical_specialty
Energy and redox metabolism [NCMLS 4]
Gd-DTPA
Iron
Transplantation
Heterologous

Blood-Volume
Capillary Permeability
03 medical and health sciences
Translational research [ONCOL 3]
medicine
Animals
Humans
business.industry
tumour
Improved Delineation
Magnetic resonance imaging
Tissue engineering and pathology [NCMLS 3]
medicine.disease
Image Enhancement
USPIO
Ferrosoferric Oxide
Tumor microenvironment [UMCN 1.3]
Functional Imaging [UMCN 1.1]
high-field MR
business
Translational Therapeutics
030217 neurology & neurosurgery
Neoplasm Transplantation
Immunity
infection and tissue repair [NCMLS 1]
Zdroj: British Journal of Cancer
British Journal of Cancer, 98, 11, pp. 1784-9
British Journal of Cancer, 98, 1784-9
ISSN: 0007-0920
Popis: Contains fulltext : 69755.pdf (Publisher’s version ) (Closed access) To enhance the success rate of antiangiogenic therapies in the clinic, it is crucial to identify parameters for tumour angiogenesis that can predict response to these therapies. In brain tumours, one such parameter is vascular leakage, which is a response to tumour-derived vascular endothelial growth factor-A and can be measured by Gadolinium-DTPA (Gd-DTPA)-enhanced magnetic resonance imaging (MRI). However, as vascular permeability and angiogenesis are not strictly coupled, tumour blood volume may be another potentially important parameter. In this study, contrast-enhanced MR imaging was performed in three orthotopic mouse models for human brain tumours (angiogenic melanoma metastases and E34 and U87 human glioma xenografts) using both Gd-DTPA to detect vascular leakage and ultrasmall iron oxide particles (USPIO) to measure blood volume. Pixel-by-pixel maps of the enhancement in the transverse relaxation rates (Delta R(2) and Delta R(2)(*)) after injection of USPIO provided an index proportional to the blood volume of the microvasculature and macrovasculature, respectively, for each tumour. The melanoma metastases were characterised by a blood volume and vessel leakage higher than both glioma xenografts. The U87 glioblastoma xenografts displayed higher permeability and blood volume in the rim than in the core. The E34 glioma xenografts were characterised by a relatively high blood volume, accompanied by only a moderate blood-brain barrier disruption. Delineation of the tumour was best assessed on post-USPIO gradient-echo images. These findings suggest that contrast-enhanced MR imaging using USPIOs and, in particular, Delta R(2) and Delta R(2)(*) quantitation, provides important additional information about tumour vasculature.
Databáze: OpenAIRE