N-(2-18F-fluoropropionyl)-l-glutamate as a potential oncology tracer for PET imaging of glioma

• Published in: Applied radiation and isotopes 2021-02, Vol.168, p.109530-109530, Article 109530
• Main Authors: Sun, Aixia, Liu, Shaoyu, Tang, Xiaolan, Pan, Qiyong, Zhang, Zhanwen, Ma, Hui, Nie, Dahong, Tang, Caihua, Tang, Ganghua
• Format: Article
• Language: English
• Subjects: Biological characterization; Glioma; N-(2-18F-fluoropropionyl)-l-glutamate; Positron emission tomography
• ISSN: 0969-8043; 1872-9800
• DOI: 10.1016/j.apradiso.2020.109530

N-(2-18F-fluoropropionyl)-l-glutamate (18F-FPGLU), a new N-substituted 18F-labeling l-glutamate, is a potential amino acid tracer for oncology PET imaging with good tumor-to-background contrast in several tumor-bearing mice. Herein, we evaluated the potential value of 18F-FPGLU for PET imaging of glioma in orthotopic glioma-bearing SD rats. A series of competitive inhibition experiments with various types of inhibitors were conducted with C6 cells to investigate the transport mechanism of 18F-FPGLU in glioma. Establishment of orthotopic rat C6 glioma-bearing SD rats models was confirmed by MRI. Then PET imaging of 18F-FPGLU was performed on the orthotopic C6 glioma-bearing SD rats and compared with that of 18F-FDG. After the rats sacrificed, the whole brain was collected and immunofluorescence staining of glial fibrillary acidic protein (GFAP) and matrix metalloproteinase 2 (MMP2) were processed. Na+-dependent system XAG- and Na+-independent system XC- are the mainly transporters of 18F-FPGLU in C6 cells. N-methyl-d-aspartate (NMDA) receptor, which is associated with the invasiveness and proliferation of glioma cells, is also involved in the uptake of 18F-FPGLU. High uptake and retention of 18F-FPGLU was observerd in orthotopic glioma with good visualization and the tumor/background ratio reached 2.35 at 60 min post-injection, which was significantly higher than that of 18F-FDG (1.72) in small-animal PET images. High expression of MMP-2 and GFAP was observed in the immunofluorescence staining of glioma xerography slices. 18F-FPGLU seems to be a better potential PET tracer than 18F-FDG for brain glioma imaging with good visualization and ability to assess the tumor activity. ●The uptake of 18F-FPGLU was primarily transported through Na+-dependent Na+-independent XAG- and XC- amino acids transporter. NMDA receptor was also involved with the transport mechanism of 18F-FPGLU in C6 cells.●Intense accumulation and retention of 18F-FPGLU was observed in the PET imaging of C6 glioma tumor-bearing mice with distinct tumor margin.●18F-FPGLU can be easily prepared and is a promising imaging agent for PET imaging glioma with good visualization and may assess the tumor invasiveness and proliferation activity.