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Signaling Pathways That Drive 18 F-FDG Accumulation in Cancer.

Authors :
Salas JR
Clark PM
Source :
Journal of nuclear medicine : official publication, Society of Nuclear Medicine [J Nucl Med] 2022 May; Vol. 63 (5), pp. 659-663. Date of Electronic Publication: 2022 Mar 03.
Publication Year :
2022

Abstract

<superscript>18</superscript> F-FDG measures glucose consumption and is an integral part of cancer management. Most cancer types upregulate their glucose consumption, yielding elevated <superscript>18</superscript> F-FDG PET accumulation in those cancer cells. The biochemical pathway through which <superscript>18</superscript> F-FDG accumulates in cancer cells is well established. However, beyond well-known regulators such as c-Myc, PI3K/PKB, and HIF1α, the proteins and signaling pathways that cancer cells modulate to activate the facilitated glucose transporters and hexokinase enzymes that drive elevated <superscript>18</superscript> F-FDG accumulation are less well understood. Understanding these signaling pathways could yield additional biologic insights from <superscript>18</superscript> F-FDG PET scans and could suggest new uses of <superscript>18</superscript> F-FDG PET in the management of cancer. Work over the past 5 years, building on studies from years prior, has identified new proteins and signaling pathways that drive glucose consumption in cancer. Here, we review these recent studies and discuss current limitations to our understanding of glucose consumption in cancer.<br /> (© 2022 by the Society of Nuclear Medicine and Molecular Imaging.)

Details

Language :
English
ISSN :
1535-5667
Volume :
63
Issue :
5
Database :
MEDLINE
Journal :
Journal of nuclear medicine : official publication, Society of Nuclear Medicine
Publication Type :
Academic Journal
Accession number :
35241480
Full Text :
https://doi.org/10.2967/jnumed.121.262609