Assessment of blood volume, vessel size, and the expression of angiogenic factors in two rat glioma models: a longitudinal in vivo and ex vivo study

Assessment of angiogenesis may help to determine tumor grade and therapy follow‐up. In vivo imaging methods for non‐invasively monitoring microvasculature evolution are therefore of major interest for tumor management. MRI evaluation of blood volume fraction (BVf) and vessel size index (VSI) was applied to assess the evolution of tumor microvasculature in two rat models of glioma (C6 and RG2). The results show that repeated MRI of BVf and VSI – which involves repeated injection of an iron‐based MR contrast agent – does not affect either the physiological status of the animals or the accuracy of the MR estimates of the microvascular parameters. The MR measurements were found to correlate well with those obtained from histology. They indicate that microvascular evolution differs significantly between the two glioma models, in good agreement with expression of angiogenic factors (vascular endothelial growth factor, angiopoietin‐2) and with activities of matrix metalloproteinases, also assessed in this study. These MRI methods thus provide considerable potential for assessing the response of gliomas to anti‐angiogenic and anti‐vascular agents, in preclinical studies as well as in the clinic. Furthermore, as differences between the fate of tumor microvasculature may underlie differences in therapeutic response, there is a need for preclinical study of several tumor models. Copyright © 2008 John Wiley & Sons, Ltd.

[1]  B. Douglas Ward,et al.  A novel technique for modeling susceptibility-based contrast mechanisms for arbitrary microvascular geometries: The finite perturber method , 2008, NeuroImage.

[2]  Samuel Valable,et al.  In vivo MRI tracking of exogenous monocytes/macrophages targeting brain tumors in a rat model of glioma , 2007, NeuroImage.

[3]  S. Powell,et al.  New immunohistochemical markers in the evaluation of central nervous system tumors: a review of 7 selected adult and pediatric brain tumors. , 2007, Archives of pathology & laboratory medicine.

[4]  Tracy T Batchelor,et al.  AZD2171, a pan-VEGF receptor tyrosine kinase inhibitor, normalizes tumor vasculature and alleviates edema in glioblastoma patients. , 2007, Cancer cell.

[5]  Grégoire Malandain,et al.  A low temperature embedding and section registration strategy for 3D image reconstruction of the rat brain from autoradiographic sections , 2006, Journal of Neuroscience Methods.

[6]  I. Jonassen,et al.  Angiogenesis-independent tumor growth mediated by stem-like cancer cells , 2006, Proceedings of the National Academy of Sciences.

[7]  T. Hirai,et al.  Diffusion-weighted imaging of metastatic brain tumors: comparison with histologic type and tumor cellularity. , 2006, AJNR. American journal of neuroradiology.

[8]  V. Tse,et al.  Recurrent glioblastoma multiforme: a review of natural history and management options. , 2006, Neurosurgical focus.

[9]  Emmanuel L Barbier,et al.  Focal brain ischemia in rat: acute changes in brain tissue T1 reflect acute increase in brain tissue water content , 2005, NMR in biomedicine.

[10]  F. Howe,et al.  A Longitudinal Study of R2* and R2 Magnetic Resonance Imaging Relaxation Rate Measurements in Murine Liver After a Single Administration of 3 Different Iron Oxide-Based Contrast Agents , 2005, Investigative Radiology.

[11]  M. Wintermark,et al.  Comparative Overview of Brain Perfusion Imaging Techniques , 2005, Journal of neuroradiology. Journal de neuroradiologie.

[12]  E. Mackenzie,et al.  VEGF-Induced BBB Permeability is Associated with an MMP-9 Activity Increase in Cerebral ischemia: Both Effects Decreased by ANG-1 , 2005, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[13]  Michael Stumm,et al.  Patupilone Induced Vascular Disruption in Orthotopic Rodent Tumor Models Detected by Magnetic Resonance Imaging and Interstitial Fluid Pressure , 2005, Clinical Cancer Research.

[14]  D. Zagzag,et al.  Angiogenesis in Gliomas: Imaging and Experimental Therapeutics , 2005, Brain pathology.

[15]  M. Wintermark,et al.  Comparative overview of brain perfusion imaging techniques. , 2005, Stroke.

[16]  H. Nakase,et al.  Vascular Endothelial Growth Factor Antagonist Reduces Brain Edema Formation and Venous Infarction , 2005, Stroke.

[17]  G. Fan,et al.  Usefulness of diffusion/perfusion-weighted MRI in rat gliomas: correlation with histopathology. , 2005, Academic radiology.

[18]  R. Strecker,et al.  Vessel size imaging in humans , 2005, Magnetic resonance in medicine.

[19]  B. D. Ward,et al.  Characterization of a first-pass gradient-echo spin-echo method to predict brain tumor grade and angiogenesis. , 2004, AJNR. American journal of neuroradiology.

[20]  Pieter Wesseling,et al.  Antiangiogenic Therapy of Cerebral Melanoma Metastases Results in Sustained Tumor Progression via Vessel Co-Option , 2004, Clinical Cancer Research.

[21]  I. Troprès,et al.  Assessment of vascular reactivity in rat brain glioma by measuring regional blood volume during graded hypoxic hypoxia , 2004, British Journal of Cancer.

[22]  Y Usson,et al.  In vivo assessment of tumoral angiogenesis , 2004, Magnetic resonance in medicine.

[23]  R Turner,et al.  Optimisation of the 3D MDEFT sequence for anatomical brain imaging: technical implications at 1.5 and 3 T , 2004, NeuroImage.

[24]  Pascale Varlet,et al.  Oligodendrogliomas. Part II: A new grading system based on morphological and imaging criteria , 1997, Journal of Neuro-Oncology.

[25]  C. Daumas-Duport,et al.  Oligodendrogliomas. Part I: Patterns of growth, histological diagnosis, clinical and imaging correlations: A study of 153 cases , 1997, Journal of Neuro-Oncology.

[26]  D. Groothuis,et al.  Blood flow and blood-to-tissue transport in 9L gliosarcomas: the role of the brain tumor model in drug delivery research , 1991, Journal of Neuro-Oncology.

[27]  R. Seitz,et al.  Vascularization of syngenic intracerebral RG2 and F98 rat transplantation tumors , 1988, Acta Neuropathologica.

[28]  Rolf F. Barth,et al.  Rat brain tumor models in experimental neuro-oncology:The 9L, C6, T9, F98, RG2 (D74), RT-2 and CNS-1 Gliomas , 2004, Journal of Neuro-Oncology.

[29]  Michal Neeman,et al.  Structural, functional, and molecular MR imaging of the microvasculature. , 2003, Annual review of biomedical engineering.

[30]  Scott D Rand,et al.  The effect of brain tumor angiogenesis on the in vivo relationship between the gradient‐echo relaxation rate change (ΔR2*) and contrast agent (MION) dose , 2003, Journal of magnetic resonance imaging : JMRI.

[31]  J. Griffiths,et al.  Effects of overexpression of dimethylarginine dimethylaminohydrolase on tumor angiogenesis assessed by susceptibility magnetic resonance imaging. , 2003, Cancer research.

[32]  K. Alitalo,et al.  Angiopoietin-2 induces human glioma invasion through the activation of matrix metalloprotease-2 , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[33]  J. Folkman Role of angiogenesis in tumor growth and metastasis. , 2002, Seminars in oncology.

[34]  M. Décorps,et al.  The Effects of Sustained Hyperventilation on Regional Cerebral Blood Volume in Thiopental-Anesthetized Rats , 2002, Anesthesia and analgesia.

[35]  Bert Grobben,et al.  Rat C6 glioma as experimental model system for the study of glioblastoma growth and invasion , 2002, Cell and Tissue Research.

[36]  P. Manow ‚The Good, the Bad, and the Ugly‘ , 2002 .

[37]  Z. Galis,et al.  This Review Is Part of a Thematic Series on Matrix Metalloproteinases, Which Includes the following Articles: Matrix Metalloproteinase Inhibition after Myocardial Infarction: a New Approach to Prevent Heart Failure? Matrix Metalloproteinases in Vascular Remodeling and Atherogenesis: the Good, the Ba , 2022 .

[38]  A P Pathak,et al.  MR‐derived cerebral blood volume maps: Issues regarding histological validation and assessment of tumor angiogenesis , 2001, Magnetic resonance in medicine.

[39]  In vivo measurement of gene expression, angiogenesis and physiological function in tumors using multiphoton laser scanning microscopy , 2001, Nature Medicine.

[40]  M. Décorps,et al.  Methodology of brain perfusion imaging , 2001, Journal of magnetic resonance imaging : JMRI.

[41]  M. Décorps,et al.  Vessel size imaging , 2001, Magnetic resonance in medicine.

[42]  P. Carmeliet,et al.  Angiogenesis in cancer and other diseases , 2000, Nature.

[43]  A P Pathak,et al.  Utility of simultaneously acquired gradient‐echo and spin‐echo cerebral blood volume and morphology maps in brain tumor patients , 2000, Magnetic resonance in medicine.

[44]  R Weissleder,et al.  Tumoral distribution of long-circulating dextran-coated iron oxide nanoparticles in a rodent model. , 2000, Radiology.

[45]  G. Lapin,et al.  Microvessel organization and structure in experimental brain tumors: microvessel populations with distinctive structural and functional properties. , 1999, Microvascular research.

[46]  M. Knopp,et al.  Estimating kinetic parameters from dynamic contrast‐enhanced t1‐weighted MRI of a diffusable tracer: Standardized quantities and symbols , 1999, Journal of magnetic resonance imaging : JMRI.

[47]  G. Yancopoulos,et al.  Vessel cooption, regression, and growth in tumors mediated by angiopoietins and VEGF. , 1999, Science.

[48]  B R Rosen,et al.  NMR imaging of changes in vascular morphology due to tumor angiogenesis , 1998, Magnetic resonance in medicine.

[49]  R. Blasberg,et al.  Imaging Experimental Brain Tumors with 1-Aminocyclopentane Carboxylic Acid and Alpha-Aminoisobutyric Acid: Comparison to Fluorodeoxyglucose and Diethylenetriaminepentaacetic Acid in Morphologically Defined Tumor Regions , 1997, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[50]  Thomas N. Sato,et al.  Angiopoietin-2, a natural antagonist for Tie2 that disrupts in vivo angiogenesis. , 1997, Science.

[51]  Katsuhiro Yamashita,et al.  Changes of relaxation times (T1, T2) and apparent diffusion coefficient after permanent middle cerebral artery occlusion in the rat: temporal evolution, regional extent, and comparison with histology , 1995, Magnetic resonance in medicine.

[52]  K. Black,et al.  Bradykinin Selectively Opens Blood-Tumor Barrier in Experimental Brain Tumors , 1994, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[53]  E F Halpern,et al.  Cerebral blood volume maps of gliomas: comparison with tumor grade and histologic findings. , 1994, Radiology.

[54]  T Kubota,et al.  Tumor vascularity in the brain: evaluation with dynamic susceptibility-contrast MR imaging. , 1993, Radiology.

[55]  C. Ellis,et al.  The functional microcirculation in a glioma model. , 1991, International journal of radiation biology.

[56]  Hermann Bondi,et al.  The good, the bad and the ugly , 1988, Nature.

[57]  S. Green,et al.  Glioblastoma multiforme and anaplastic astrocytoma pathologic criteria and prognostic implications , 1985, Cancer.

[58]  J. Swenberg,et al.  Quantitative aspects of transplacental tumor induction with ethylnitrosourea in rats. , 1972, Cancer research.

[59]  W. Sweet,et al.  Morphological and immunochemical studies of rat glial tumors and clonal strains propagated in culture. , 1971, Journal of neurosurgery.

[60]  S. Meiboom,et al.  Modified Spin‐Echo Method for Measuring Nuclear Relaxation Times , 1958 .