PET Imaging of Hepatocellular Carcinomas: 18 F-Fluoropropionic Acid as a Complementary Radiotracer for 18 F-Fluorodeoxyglucose

To evaluate the preclinical value of F-fluoropropionic acid ( F-FPA) and F-fluorodeoxyglucose ( F-FDG) positron emission tomography (PET) for imaging HCCs. The F-FPA and F-FDG uptake patterns in 3 HCC cell lines (Hep3B, HepG2, and SK-Hep1) were assessed in vitro and in vivo. The F-FPA uptake mechanism was investigated using inhibition experiments with orlistat and 5-tetradecyloxy-2-furoic acid. The F-FPA PET imaging was performed in different tumor animal models and compared with F-FDG. We also evaluated the expressions of glucose transporter-1 (GLUT1), fatty acid synthase (FASN), and matrix metalloproteinase-2 (MMP2) in these cell lines. In vitro experiments showed that the radiotracer uptake patterns were complementary in the HCC cell lines. Orlistat and 5-tetradecyloxy-2-furoic acid decreased the uptake of F-FPA. The tumor-to-liver ratio of F-FPA was superior to that of F-FDG in the SK-Hep1 and HepG2 tumors ( P < .05). However, in the Hep3B tumors, the tumor-to-liver normalized uptake of F-FDG was higher than F-FPA ( P < .01). FASN was highly expressed in cell lines with high F-FPA uptake, whereas GLUT1 was highly expressed in cell lines with high F-FDG uptake. The F-FPA uptake correlated with FASN ( r = 0.89, P = .014) and MMP2 ( r = 0.77, P = .002) expressions. PET imaging with F-FPA combined with F-FDG can be an alternative for detecting HCC.