Journal article
Investigating tumor perfusion by hyperpolarized (13) C MRI with comparison to conventional gadolinium contrast-enhanced MRI and pathology in orthotopic human GBM xenografts: Correlation of13C Perfusion Imaging and Gd-Enhanced Contrast MRI
University of California at San Diego1
Center for Hyperpolarization in Magnetic Resonance, Centers, Technical University of Denmark2
Department of Electrical Engineering, Technical University of Denmark3
Center for Magnetic Resonance, Department of Electrical Engineering, Technical University of Denmark4
Massachusetts Institute of Technology5
Dissolution dynamic nuclear polarization (DNP) enables the acquisition of (13) C magnetic resonance data with a high sensitivity. Recently, metabolically inactive hyperpolarized (13) C-labeled compounds have shown to be potentially useful for perfusion imaging. The purpose of this study was to validate hyperpolarized perfusion imaging methods by comparing with conventional gadolinium (Gd)-based perfusion MRI techniques and pathology.
Dynamic (13) C data using metabolically inactive hyperpolarized bis-1,1-(hydroxymethyl)-[1-(13) C]cyclopropane-d8 (HMCP) were obtained from an orthotopic human glioblastoma (GBM) model for the characterization of tumor perfusion and compared with standard Gd-based dynamic susceptibility contrast (DSC) MRI data and immunohistochemical analysis from resected brains.
Distinct HMCP perfusion characteristics were observed within the GBM tumors compared with contralateral normal brain tissue. The perfusion parameters obtained from the hyperpolarized HMCP data in tumor were strongly correlated with normalized peak height measured from the DSC images. The results from immunohistochemical analysis supported these findings by showing a high level of vascular staining for tumor that exhibited high levels of hyperpolarized HMCP signal.
The results from this study have demonstrated that hyperpolarized HMCP data can be used as an indicator of tumor perfusion in an orthotopic xenograft model for GBM. Magn Reson Med, 2016. © 2016 Wiley Periodicals, Inc.
Language: | English |
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Year: | 2016 |
Pages: | 841-847 |
ISSN: | 15222594 and 07403194 |
Types: | Journal article |
DOI: | 10.1002/mrm.26155 |
ORCIDs: | Ardenkjær-Larsen, Jan Henrik |