L-Glutamine (Gln) has many important functions in the normal physiology, but its role in cancer biology has created a demand for glutamine PET tracers (Zhu et al., 2017), such as (2S,4R)-4-[18F]fluoroglutamine ([18F]FGln) (Lieberman et al., 2011; Venneti et al., 2015). In contrast to L-glutamine, 18F-labelled glutamine analogues are not metabolized in the TCA cycle, but can be incorporated into proteins and peptides (Yang et al., 2017), and can be used assess transporter (ASCT2) activity or protein synthesis rate.
Human trials with [18F]FGln PET have provided promising results, with high uptake in aggressive tumours in several cancer types (Venneti et al., 2015; Dunphy et al., 2018). Fasting prior to PET study is not required, because tumour uptake was not decreased in non-fasting patients (Dunphy et al., 2018); there even seems to be a trend of increased tumour uptake in non-fasting patients compared to the fasting patients, possibly due to competition at transport or enzymatic processes.
[18F]FGln is mainly transported by ASCT2, as shown by reduction of tracer uptake caused by ASCT2 inhibitor GPNA (Lieberman et al., 2011), and correlation of tumour uptake and ASCT2 expression (Hassanein et al., 2016). Impaired BBB or neuroinflammation do not lead to increased [18F]FGln uptake in brain models (Zhu et al., 2017). Cytoplasmic glutaminase can metabolize [18F]FGln into [18F]fluoroglutamate, which can further be transformed into α-ketoglutarate by alanine aminotransferase (AAT), with the loss of [18F]F- (Ploesll et al., 2012). Like L-glutamine, [18F]FGln can be transported from cytoplasm into mitochondria; mitochondrial enzymes transform it there again into [18F]fluoroglutamate, but the next step produces [18F]fluoro-α-ketoglutarate and does not lead to release of [18F]F- (Cooper et al., 2012). The fraction of [18F]FGln metabolites trapped in tumour cells is relatively low after one hour in animal model (Zhou et al., 2017). [18F]FGln seems not to be a good substrate for glutaminase, and its uptake represents mostly the glutamine transport and intracellular glutamine pool size (Zhu et al., 2017). Mitochondrial glutaminase is the rate-limiting step in tumour cells ability to use glutamate in the TCA cycle, and small-molecule inhibitors for this enzyme have been developed. Inhibiting the enzyme leads to increased glutamate pool in the cytoplasm, which leads to increased competition for efflux, and can be seen as increased [18F]FGln uptake in the tumours of mice (Zhou et al., 2017).
The radioactivity uptake one hour after [18F]FGln injection is highest in the bone marrow and pancreas, and high also in the liver, heart muscle, and small intestine; (Dunphy et al., 2018). Excretion into urine is fast, and probably prevents the usage in imaging tumours close to urinary bladder. Uptake in the kidneys is very high, but decreases by time (Lieberman et al., 2011).
After bolus injection, 18F is cleared from the blood and plasma in biphasic manner (Dunphy et al., 2018).
Blood-to-plasma ratio, which may be needed for conversion of blood to plasma concentrations or vice versa, was 0.74±0.2 at 5 min and 0.81±0.3 at 60 min after tracer injection (Dunphy et al., 2018). The ratio at 5 min is higher than would be obtained if 18F were in the plasma alone; that, and the the slow increase of the ratio is probably due to the free [18F]F-, which is known to be transported across the red blood cell membrane. The increase and the high variability in the ratios suggests that population-based blood-to-plasma transformation is not feasible.
Parent tracer fractions in plasma, as measured with HPLC, were 86±19% at 1 min, 88±9% at 5 min, 81±8% at 15 min, and 65±21% at 30 min after injection; practically all the rest radioactivity in the plasma was due to free [18F]F- (Dunphy et al., 2018). The percentage of radioactivity trapped in the plasma pellet increased from ∼10% at 1 min to ∼26% at 30 min, suggesting that it is due to labelled polypeptides (Dunphy et al., 2018).
The fast defluorination causes marked uptake in the bones; at 60 min, the bone uptake was about half of the uptake seen in [18F]NaF PET studies (Dunphy et al., 2018). Blocking of the 2-amino group of [18F]FGln by formation of dipeptide can greatly improve the in vitro stability of the tracer, while after venous administration [18F]FGln is quicly released from the dipeptide (Zha et al., 2018), but this will probably not help to solve the problem of in vivo defluorination.
Data analysis methods
Detailed modelling of [18F]FGln PET data may not be feasible, because the injected dose may not be pure (2S,4R)-4-[18F]fluoroglutamine, but may contain marked proportion of its stereoisomer, (2R,4R)-4-[18F]fluoroglutamine, which as an analogue of D-glutamine has very different pharmacokinetics and slower tissue uptake. Logan plot and two-compartment model in a mice study suggests that tumour uptake is reversible (Zhou et al., 2017), with further supports the use of [18F]FGln as a probe of glutamine transport, and not for measurement of protein synthesis rate.
High bone uptake may hinder the analysis of tumours that are close to bone, especially in the cortex of the brain.
In human cancer studies SUV peak method and tumour-to-plasma ratio have been used (Dunphy et al., 2018). In oncological brain studies, where healthy brain area is available, it has been used as reference region in calculation of SUV ratio (Venneti et al., 2015).
Adapted SUV peak method has been used in animal tumour models (Zhou et al., 2017). Tumour-to-blood ratio can be used to detect the increased tumour cell glutamate pool after glutaminase inhibition (Zhou et al., 2017).
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Created at: 2018-02-28
Updated at: 2018-03-03
Written by: Vesa Oikonen, Anne Roivainen