Two-Chain Mature Hepatocyte Growth Factor-Specific Positron Emission Tomography Imaging in Tumors Using 64 Cu-Labeled HiP-8, a Nonstandard Macrocyclic Peptide Probe.
Shota WarashinaHiroki SatoMaki ZoudaMaiko TakahashiYasuhiro WadaToby PassiouraHiroaki SugaYasuyoshi WatanabeKunio MatsumotoHidefumi MukaiPublished in: Molecular pharmaceutics (2023)
Two-chain hepatocyte growth factor (tcHGF), the mature form of HGF, is associated with malignancy and anticancer drug resistance; therefore, its quantification is an important indicator for cancer diagnosis. In tumors, activated tcHGF hardly discharges into the systemic circulation, indicating that tcHGF is an excellent target for molecular imaging using positron emission tomography (PET). We recently discovered HGF-inhibitory peptide-8 (HiP-8) that binds specifically to human tcHGF with nanomolar affinity. The purpose of this study was to investigate the usefulness of HiP-8-based PET probes in human HGF knock-in humanized mice. 64 Cu-labeled HiP-8 molecules were synthesized using a cross-bridged cyclam chelator, CB-TE1K1P. Radio-high-performance liquid chromatography-based metabolic stability analyses showed that more than 90% of the probes existed in intact form in blood at least for 15 min. In PET studies, significantly selective visualization of hHGF-overexpressing tumors versus hHGF-negative tumors was observed in double-tumor-bearing mice. The accumulation of labeled HiP-8 into the hHGF-overexpressing tumors was significantly reduced by competitive inhibition. In addition, the radioactivity and distribution of phosphorylated MET/HGF receptor were colocalized in tissues. These results demonstrate that the 64 Cu-labeled HiP-8 probes are suitable for tcHGF imaging in vivo, and secretory proteins like tcHGF can be a target for PET imaging.
Keyphrases
- pet imaging
- positron emission tomography
- growth factor
- computed tomography
- total hip arthroplasty
- high performance liquid chromatography
- endothelial cells
- pet ct
- small molecule
- fluorescence imaging
- living cells
- high resolution
- gene expression
- adipose tissue
- type diabetes
- young adults
- simultaneous determination
- squamous cell carcinoma
- tandem mass spectrometry
- nucleic acid
- induced pluripotent stem cells
- solid phase extraction
- binding protein
- metabolic syndrome