Lin Zhu, Karl Ploessl, Rong Zhou, David Mankoff, Hank F Kung
Journal: Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2017;58(4):533-537
PMID: 28232608
Glucose and glutamine are the most abundant nutrients for producing energy and building blocks in normal and tumor cells. Increased glycolysis in tumors, the Warburg Effect, is the basis for F-FDG PET imaging. Cancer cells can also be genetically reprogrammed to use glutamine. 5-C-(2)-glutamine and F-(2,4)4-fluoroglutamine may be useful complementary tools to measure changes in tumor metabolism. In glioma patients, the tracer F-(2,4)4-fluoroglutamine showed tumor-to-background contrast different from that of F-FDG and differences in uptake in glioma patients with clinical progression of disease versus stable disease (tumor-to-brain ratio > 3.7 in clinically active glioma tumors, minimal or no specific uptake in clinically stable tumors). These preliminary results suggest that F-(2,4)4-fluoroglutamine PET may be a new tool for probing in vivo metabolism of glutamine in cancer patients and for guiding glutamine-targeted therapeutics. Further studies of uptake mechanism, and comparison of kinetics for F-(2,4)4-fluoroglutamine versus the C-labeled native glutamine, will be important and enlightening.
© 2017 by the Society of Nuclear Medicine and Molecular Imaging.
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