Author(s)

T. A. D. Smith, M. Zanda, I. N. Fleming

ISBN

0969-8051

Publication year

2013

Periodical

Nuclear Medicine and Biology

Periodical Number

6

Volume

40

Pages

858-864

Author Address

Fleming, IN Aberdeen Biomed Imaging Ctr, Aberdeen AB25 2ZD, Scotland Univ Aberdeen, Sch Med & Dent, Div Appl Med, Aberdeen AB25 2ZD, Scotland Univ Aberdeen, Sch Med Sci, Inst Med Sci, Kosterlitz Ctr Therapeut, Aberdeen AB25 2ZD, Scotland Aberdeen Biomed Imaging Ctr, Aberdeen AB25 2ZD, Scotland

Full version

Introduction: Hypoxia can stimulate F-18-fluorodeoxyglucose (FDG) uptake in cultured cells. A better understanding of the underlying molecular mechanism is required to determine the value of FDG for studying tumour hypoxia.
Methods: The effect of hypoxia on FDG uptake, and key proteins involved in glucose transport and glycolysis, was studied in MCF7 and MDA231 breast cancer cell lines.
Results: Hypoxia induced a dose- and time-dependent increase in FDG uptake. The FOG increase was transient, suggesting that FDG uptake is only likely to be increased by acute hypoxia (<24 h). Molecular analysis indicated that hypoxia upregulated glut1 and 6-phosphofructo-2-kinase, key proteins involved in regulating glucose transport and glycolysis, and that these changes were induced by Hypoxia-Inducible factor 1 (HIF1) upregulation and/or AMP-activated protein kinase activation. Conclusions: FDG may provide useful information about the oxygenation status of cells in hypoxic regions where HIF1 upregulation is hypoxia-driven. (C) 2013 Elsevier Inc. All rights reserved.