| Literature DB >> 29541356 |
Neydher Berroterán-Infante1,2, Theresa Balber1,3, Petra Fürlinger1, Michael Bergmann4, Rupert Lanzenberger5, Marcus Hacker1, Markus Mitterhauser1,3,6, Wolfgang Wadsak1,2,7.
Abstract
The overexpression of the translocator protein (TSPO) has been amply reported for a variety of conditions, including neurodegenerative disorders, heart failure, and cancer. Thus, TSPO has been proposed as an excellent imaging biomarker, allowing, in this manner, to obtain an accurate diagnosis and to follow disease progression and therapy response. Accordingly, several radioligands have been developed to accomplish this purpose. In this work, we selected [18F]FEPPA, as one of the clinical established tracers, and assessed its in vitro performance in colorectal cancer. Moreover, we setup an improved radiosynthesis method and assessed the in vitro binding affinity of the nonradioactive ligand toward the human TSPO. Our results show an excellent to moderate affinity, in the subnanomolar and nanomolar range, as well as the suitability of [18F]FEPPA as an imaging agent for the TSPO in colorectal cancer.Entities:
Year: 2018 PMID: 29541356 PMCID: PMC5846029 DOI: 10.1021/acsmedchemlett.7b00367
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345