| Literature DB >> 32415874 |
Jae Won Chang1,2, Mohammed Bhuiyan3, Hsiu-Ming Tsai4, Hannah J Zhang4,3, Gang Li1, Shaghayegh Fathi1, David C McCutcheon1, Lara Leoni4, Richard Freifelder3, Chin-Tu Chen4,3, Raymond E Moellering1.
Abstract
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.Entities:
Keywords: NCEH1; activity-based probes; imaging; positron emission tomography; radiotracers
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Year: 2020 PMID: 32415874 PMCID: PMC7748380 DOI: 10.1002/anie.202004762
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336