In Vivo Imaging of the Tumor-Associated Enzyme NCEH1 with a Covalent PET Probe.
Jae Won ChangMohammed BhuiyanHsiu-Ming TsaiHannah J ZhangGang LiShaghayegh FathiDavid C McCutcheonLara LeoniRichard FreifelderChin-Tu ChenRaymond E MoelleringPublished in: Angewandte Chemie (International ed. in English) (2020)
Herein, we report the development of an 18 F-labeled, activity-based small-molecule probe targeting the cancer-associated serine hydrolase NCEH1. We undertook a focused medicinal chemistry campaign to simultaneously preserve potent and specific NCEH1 labeling in live cells and animals, while permitting facile 18 F radionuclide incorporation required for PET imaging. The resulting molecule, [18 F]JW199, labels active NCEH1 in live cells at nanomolar concentrations and greater than 1000-fold selectivity relative to other serine hydrolases. [18 F]JW199 displays rapid, NCEH1-dependent accumulation in mouse tissues. Finally, we demonstrate that [18 F]JW199 labels aggressive cancer tumor cells in vivo, which uncovered localized NCEH1 activity at the leading edge of triple-negative breast cancer tumors, suggesting roles for NCEH1 in tumor aggressiveness and metastasis.
Keyphrases
- pet imaging
- induced apoptosis
- small molecule
- cell cycle arrest
- quantum dots
- positron emission tomography
- gene expression
- high resolution
- endoplasmic reticulum stress
- computed tomography
- living cells
- cell death
- signaling pathway
- squamous cell carcinoma
- young adults
- reduced graphene oxide
- pi k akt
- fluorescence imaging
- fluorescent probe