| Literature DB >> 31017386 |
Justin J Bailey1, Lena Kaiser2, Simon Lindner2, Melinda Wüst1, Alexander Thiel3,4, Jean-Paul Soucy3, Pedro Rosa-Neto5, Peter J H Scott6, Marcus Unterrainer2, David R Kaplan7, Carmen Wängler8, Björn Wängler9, Peter Bartenstein2, Vadim Bernard-Gauthier1, Ralf Schirrmacher1.
Abstract
The tropomyosin receptor kinase TrkA/B/C family is responsible for human neuronal growth, survival, and differentiation from early nervous system development stages onward. Downregulation of TrkA/B/C receptors characterizes numerous neurological disorders including Alzheimer's disease (AD). Abnormally expressed Trk receptors or chimeric Trk fusion proteins are also well-characterized oncogenic drivers in a variety of neurogenic and non-neurogenic human neoplasms and are currently the focus of intensive clinical research. Previously, we have described the clinical translation of a highly selective and potent carbon-11-labeled pan-Trk radioligand and the preclinical characterization of the optimized fluorine-18-labeled analogue, [18F]TRACK, for in vivo Trk positron emission tomography (PET) imaging. We describe herein central nervous system selectivity assessment and first-in-human study of [18F]TRACK.Entities:
Keywords: PET; Trk; Tropomyosin receptor kinase; copper-mediated radiofluorination; fluorine-18; kinase inhibitor; neuroimaging; positron emission tomography
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Year: 2019 PMID: 31017386 DOI: 10.1021/acschemneuro.9b00144
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418