[18F]-2-fluoro-2-deoxyglucose transport kinetics as a function of extracellular glucose concentration in malignant glioma, fibroblast and macrophage cells in vitro
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作者:
Burrows, RC
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机构:Univ Washington, Dept Neurol, Seattle, WA 98195 USA
Burrows, RC
Freeman, SD
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机构:Univ Washington, Dept Neurol, Seattle, WA 98195 USA
Freeman, SD
Charlop, AW
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机构:Univ Washington, Dept Neurol, Seattle, WA 98195 USA
Charlop, AW
Wiseman, RW
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机构:Univ Washington, Dept Neurol, Seattle, WA 98195 USA
Wiseman, RW
Adamsen, TCH
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机构:Univ Washington, Dept Neurol, Seattle, WA 98195 USA
Adamsen, TCH
Krohn, KA
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机构:Univ Washington, Dept Neurol, Seattle, WA 98195 USA
Krohn, KA
Spence, AM
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Univ Washington, Dept Neurol, Seattle, WA 98195 USAUniv Washington, Dept Neurol, Seattle, WA 98195 USA
Spence, AM
[1
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机构:
[1] Univ Washington, Dept Neurol, Seattle, WA 98195 USA
[2] Univ Washington, Dept Radiol, Mol Imaging Res Ctr, Seattle, WA 98195 USA
[3] Michigan State Univ, Dept Physiol, Mol Imaging Res Ctr, E Lansing, MI 48824 USA
[4] Michigan State Univ, Dept Radiol, Mol Imaging Res Ctr, E Lansing, MI 48824 USA
FDG-PET is used to measure the metabolic rate of glucose. Transport and phosphorylation determine the amount of hexose analog that is phosphorylated and trapped. Competition occurs for both events, such that extracellular glucose concentration affects the FDG image. This study investigated the effect of glucose concentration on the rate of FDG accumulation in three cell lines. The results show that extracellular glucose concentration has a greater impact on the rate of FDG accumulation than the relative abundance of GLUT transporter subtypes. (C) 2004 Elsevier Inc., All rights reserved.