Intracellular water residence time (τi) is an important property of solid tumors, with implications in cellular energy turnover. Measurement of τi using the active contrast encoding MRI method offers insight into tumor microenvironment heterogeneity and potentially metabolic activity. Our study compares τi, measured using ACE-MRI, in mouse gliomas with the standardized uptake value (SUV) from 18F-FDG PET in order to investigate the feasibility of using τi as an imaging marker for cellular metabolic activity.
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