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Radiosynthesis, in vitro and preliminary biological evaluation of [ 18 F]2‐amino‐4‐((2‐((3‐fluorobenzyl)oxy)benzyl)(2‐((3‐(fluoromethyl)benzyl)oxy)benzyl)amino)butanoic acid, a novel alanine serine cysteine transporter 2 inhibitor‐based positron emission tomography tracer
Author(s) -
Baguet Tristan,
Bouton Jakob,
Janssens Jonas,
Pauwelyn Glenn,
Verhoeven Jeroen,
Descamps Benedicte,
Van Calenbergh Serge,
Vanhove Christian,
De Vos Filip
Publication year - 2020
Publication title -
journal of labelled compounds and radiopharmaceuticals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.432
H-Index - 47
eISSN - 1099-1344
pISSN - 0362-4803
DOI - 10.1002/jlcr.3863
Subject(s) - chemistry , radiosynthesis , amino acid transporter , in vivo , in vitro , amino acid , glutamine , alanine , positron emission tomography , benzyl bromide , stereochemistry , transporter , biochemistry , nuclear medicine , microbiology and biotechnology , biology , gene , catalysis , medicine
The metabolic alterations in tumors make it possible to visualize the latter by means of positron emission tomography, enabling diagnosis and providing metabolic information. The alanine serine cysteine transporter‐2 (ASCT‐2) is the main transporter of glutamine and is upregulated in several tumors. Therefore, a good positron emission tracer targeting this transport protein would have substantial value. Hence, the aim of this study is to develop a fluorine‐18‐labeled version of a V‐9302 analogue, one of the most potent inhibitors of ASCT‐2. The precursor was labeled with fluorine‐18 via a nucleophilic substitution of the corresponding benzylic bromide. The cold reference product was subjected to in vitro assays with [ 3 H]glutamine in a PC‐3 and F98 cell line to determine the affinity for both the human and rat ASCT‐2. To evaluate the tracer potential dynamic μPET, images were acquired in a mouse xenograft model for prostate cancer. The tracer could be synthesized with an overall nondecay corrected yield of 3.66 ± 1.90%. in vitro experiments show inhibitor constants K i of 90 and 125 μM for the PC‐3 and F98 cells, respectively. The experiments in the PC‐3 xenograft demonstrate a low uptake in the tumor tissue. We have successfully synthesized the radiotracer [ 18 F]2‐amino‐4‐((2‐((3‐fluorobenzyl)oxy)benzyl)(2‐((3‐(fluoromethyl)benzyl)oxy)benzyl)amino)butanoic acid. in vitro experiments show a good affinity for both the human and rat ASCT‐2. However, the tracer suffers from poor in vivo tumor uptake in the PC‐3 model. Briefly, we present the first fluorine‐18‐labeled derivative of compound V‐9302, a promising novel ASCT‐2 blocker used for inhibition of tumor growth.