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MR Molecular Imaging of Prostate Cancer with a Small Molecular CLT1 Peptide Targeted Contrast Agent
Published on: September 3, 2013
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Propionic Acid-Based PET Imaging of Prostate Cancer
Zhanwen Zhang1,2, Shaoyu Liu2,3, Hui Ma2,4
1Department of Nuclear Medicine, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510655, China.
Molecular Imaging and Biology
|April 20, 2021
Summary
This study shows that 2-[18F]fluoropropionic acid (18F-FPA) PET imaging may be a valuable tool for prostate cancer (PCa) diagnosis. 18F-FPA uptake varied with fatty acid synthase activity and was reduced by a FASN inhibitor.
Area of Science:
- Nuclear medicine
- Oncology
- Radiochemistry
Background:
- Prostate cancer (PCa) diagnosis relies on imaging techniques.
- Fatty acid synthase (FASN) is implicated in cancer progression.
- Novel PET imaging agents are needed for PCa detection.
Purpose of the Study:
- To evaluate 2-[18F]fluoropropionic acid (18F-FPA) for PET imaging of PCa.
- To explore the relationship between 18F-FPA accumulation and FASN levels in PCa models.
- To report the first human PET study using 18F-FPA in a PCa patient.
Main Methods:
- Cell culture of PCa lines (LNCaP, PC-3, DU145) with varying FASN expression.
- PET imaging comparison of 18F-FPA and 18F-FDG in PCa models.
- In vivo experiments using orlistat (FASN inhibitor).
- Human PET study in a PCa patient using 18F-FPA and 18F-FDG.
Main Results:
- 18F-FPA uptake was higher than 18F-FDG in LNCaP and PC-3 tumors (P<0.05).
- 18F-FPA uptake was lower than 18F-FDG in DU145 tumors (P<0.05).
- Orlistat treatment reduced 18F-FPA accumulation in all tested PCa models.
- 18F-FPA showed higher uptake than 18F-FDG in the first PCa patient.
Conclusions:
- 18F-FPA uptake in PCa models correlates with FASN activity.
- 18F-FPA accumulation decreased after FASN inhibition.
- 18F-FPA shows potential as a broad-spectrum PET imaging agent for PCa diagnosis.
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