Hyperpolarized 13C magnetic resonance metabolic imaging: Application to brain tumors

Ilwoo Park*, Peder E Z Larson, Matthew L. Zierhut, Simon Hu, Robert Bok, Tomoko Ozawa, John Kurhanewicz, Daniel B. Vigneron, Scott R. VandenBerg, C. David James, Sarah J. Nelson

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

128 Scopus citations

Abstract

In order to compare in vivo metabolism between malignant gliomas and normal brain, 13C magnetic resonance (MR) spectroscopic imaging data were acquired from rats with human glioblastoma xenografts (U-251 MG and U-87 MG) and normal rats, following injection of hyperpolarized [1-13C]-pyruvate. The median signalto-noise ratio (SNR) of lactate, pyruvate, and total observed carbon-13 resonances, as well as their relative ratios, were calculated from voxels containing Gadolinium-enhanced tissue in T1 postcontrast images for rats with tumors and from normal brain tissue for control rats. [1-13C]-labeled pyruvate and its metabolic product, [1- 13C]-lactate, demonstrated significantly higher SNR in the tumor compared with normal brain tissue. Statistical tests showed significant differences in all parameters (P < .0004) between the malignant glioma tissue and normal brain. The SNR of lactate, pyruvate, and total carbon was observed to be different between the U-251 MG and U-87 MG models, which is consistent with inherent differences in the molecular characteristics of these tumors. These results suggest that hyperpolarizedMRmetabolic imaging may be valuable for assessing prognosis and monitoring response to therapy for patients with brain tumors.

Original languageEnglish (US)
Pages (from-to)133-144
Number of pages12
JournalNeuro-oncology
Volume12
Issue number2
DOIs
StatePublished - Feb 2010

Keywords

  • Brain tumor
  • Dynamic nuclear polarization (DNP)
  • Human glioblastoma xenograft
  • Hyperpolarized carbon-13 metabolic imaging

ASJC Scopus subject areas

  • Oncology
  • Clinical Neurology
  • Cancer Research

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