11C-Acetate PET/CT Imaging Physiologic Uptake, Variants, and PitfallsTools Karanikas, Georgios und Beheshti, Mohsen (2014) 11C-Acetate PET/CT Imaging Physiologic Uptake, Variants, and Pitfalls. PET Clinics, 9. pp. 339-344.
Text (11C-Acetate PET/CT Imaging Physiologic Uptake, Variants, and Pitfalls)
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� 11C-acetate is a biomarker for cell membrane lipid synthesis and may increase in various
malignancies.
� Enhanced uptake is observed in salivary glands, tonsils, meningeal tuberculoma, meningiomas,
macroadenomas of pituitary gland, and benign thyroid nodes.
� Reactive lymphadenopathy in mediastinum and hilum shows mild to moderate 11C-acetate
accumulation.
� Pancreas, spleen, and liver show an increased uptake of 11C-acetate; however, pancreatitis is
related with reduced tracer accumulation.
� Proliferative or granulomatous cystitis may be present with enhanced 11C-acetate tracer
accumulation.
This article describes the physiologic distribution
of 11C-acetate and discusses regions that occasionally
may present increased activity not related
to tumor tissue or owing to other nononcologic
findings. The short half-life of 11C-acetate (20 min)
warrants an onsite cyclotron. Hence, there are
less data available comparing 18F-labeled PET
tracers.
11C-acetate PET has been used to measure
myocardial oxygen consumption and to study prostate
cancer (PCa), hepatocellular carcinoma (HCC),
renal cell carcinoma (RCC), bladder carcinoma,
and brain tumors.1 There are also rare conditions
that have been incidentally depicted by 11C-acetate
PET, such as thymoma,2 cerebellopontine angle
schwannoma,3 angiomyolipoma of the kidney,4
and encephalitis.5 Assessment ofmultiple myeloma
has also been studied by this tracer.6
Acetate is a molecule quickly picked up by cells
and converted into acetyl-CoA by acetyl-CoA synthetase.
1 It is used to synthesize cholesterol and
fatty acids, thus forming cell membrane (anabolic
pathway), or is oxidized (catabolic pathway) in
mitochondria by the tricarboxylic acid (TCA) cycle
to CO2 and H2O, thus producing energy. The predominant
pathway is strictly linked with the type of
cell; in myocardial tissue, acetate is mainly metabolized
to CO2 via the TCA cycle,7 whereas tumor
cells overexpress the enzyme fatty acid synthetase,
thus converting most of the acetate into fatty
acids and incorporating them into intracellular
phosphatidylcholine membrane microdomains
that are important for tumor growth and metastasis.
8 For nuclear medicine purposes, acetate is
labeled with 11C, and the derived compound is
called 11C-acetate.
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