Dynamic, contrast-enhanced perfusion MRI in mouse gliomas: correlation with histopathology

Cha, Soonmee, Johnson, Glyn, Wadghiri, Youssef Zaim, Jin, Olivier, Babb, Jim, Zagzag, David and Turnbull, Daniel H. (2003) Dynamic, contrast-enhanced perfusion MRI in mouse gliomas: correlation with histopathology. Magnetic Resonance in Medicine, 49 (5). pp. 848-855. ISSN 0740-3194

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Abstract

The aim of this study was to develop an MRI protocol to evaluate the growth and vascularity of implanted GL261 mouse gliomas on a 7T microimaging system. Both conventional T(1)- and T(2)-weighted imaging and dynamic, contrast-enhanced T(2)*-weighted imaging were performed on 34 mice at different stages of tumor development. MRI measurements of relative cerebral blood volume (rCBV) were compared to histological assessments of microvascular density (MVD). Enhancement on postcontrast T(1)-weighted images was compared to histological assessments of Evan's blue extravasation. Conventional T(2)-weighted and postcontrast T(1)-weighted images demonstrated tumor growth characteristics consistent with previous descriptions of GL261 glioma. Furthermore, measurements of rCBV from MRI data were in good agreement with histological measurements of MVD from the same tumors. Postcontrast enhancement on T(1)-weighted images was observed at all stages of GL261 glioma progression, even before evidence of angiogenesis, indicating that the mechanism of conventional contrast enhancement in MRI does not require neovascularization. These results provide quantitative support for MRI approaches currently used to assess human brain tumors, and form the basis for future studies of angiogenesis in genetically engineered mouse brain tumor models.

Item Type: Article
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
University of East Anglia > Faculty of Medicine and Health Sciences > Research Groups > Clinical Science and Trials
Depositing User: Pure Connector
Date Deposited: 28 Sep 2015 14:54
Last Modified: 25 Jul 2018 11:06
URI: https://ueaeprints.uea.ac.uk/id/eprint/54436
DOI: 10.1002/mrm.10446

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