PET imaging of glutaminolysis in tumors by 18F-(2S,4R)4- fluoroglutamine Journal Article


Authors: Lieberman, B. P.; Ploessl, K.; Wang, L.; Qu, W.; Zha, Z.; Wise, D. R.; Chodosh, L. A.; Belka, G.; Thompson, C. B.; Kung, H. F.
Article Title: PET imaging of glutaminolysis in tumors by 18F-(2S,4R)4- fluoroglutamine
Abstract: Changes in gene expression, metabolism, and energy requirements are hallmarks of cancer growth and self-sufficiency. Upregulation of the PI3K/Akt/mTor pathway in tumor cells has been shown to stimulate aerobic glycolysis, which has enabled 18F-FDG PET tumor imaging. However, of the millions of 18F-FDG PET scans conducted per year, a significant number of malignant tumors are 18F-FDG PET-negative. Recent studies suggest that several tumors may use glutamine as the key nutrient for survival. As an alternative metabolic tracer for tumors, 18F-(2S,4R)4- fluoroglutamine was developed as a PET tracer for mapping glutaminolytic tumors. Methods: A series of in vitro cell uptake and in vivo animal studies were performed to demonstrate tumor cell addiction to glutamine. Cell uptake studies of this tracer were performed in SF188 and 9L glioblastoma tumor cells. Dynamic small-animal PET studies of 18F-(2S,4R)4-fluoroglutamine were conducted in 2 animal models: xenografts produced in F344 rats by subcutaneous injection of 9L tumor cells and transgenic mice with M/tomND spontaneous mammary gland tumors. Results: In vitro studies showed that both transformed 9L and SF188 tumor cells displayed a high rate of glutamine uptake (maximum uptake, ≈16% dose/100 μg of protein). The cell uptake of 18F-(2S,4R)4- fluoroglutamine by SF188 cells is comparable to that of 3H-L- glutamine but higher than that of 18F-FDG. The tumor cell uptake can be selectively blocked. Biodistribution and PET studies showed that 18F-(2S,4R)4-fluoroglutamine localized in tumors with a higher uptake than in surrounding muscle and liver tissues. Data suggest that certain tumor cells may use glutamine for energy production. Conclusion: The results support that 18F-(2S,4R)4-fluoroglutamine is selectively taken up and trapped by tumor cells. It may be useful as a novel metabolic tracer for tumor imaging. Copyright © 2011 by the Society of Nuclear Medicine, Inc.
Keywords: controlled study; unclassified drug; nonhuman; positron emission tomography; mouse; animals; mice; animal tissue; gene expression; animal experiment; animal model; in vivo study; in vitro study; tumor xenograft; cell line, tumor; breast neoplasms; mice, transgenic; cell transformation, neoplastic; drug distribution; isotope labeling; cell transformation; glioblastoma; rat; fluorodeoxyglucose f 18; positron-emission tomography; tumor cell; radiopharmaceutical agent; rats; c-myc; cell transport; pet; cell metabolism; cell activity; biological transport; glutamine; 18f-fdg; energy yield; tumor metabolism; amino acid metabolism; 4 fluoroglutamine f 18; glutaminolysis
Journal Title: Journal of Nuclear Medicine
Volume: 52
Issue: 12
ISSN: 0161-5505
Publisher: Society of Nuclear Medicine  
Date Published: 2011-12-01
Start Page: 1947
End Page: 1955
Language: English
DOI: 10.2967/jnumed.111.093815
PUBMED: 22095958
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 3" - "Export Date: 25 June 2012" - "CODEN: JNMEA" - "Source: Scopus"
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  1. Craig Bernie Thompson
    153 Thompson