| Literature DB >> 32568549 |
Aikaterini Kaloudi1, Panagiotis Kanellopoulos1, Thorsten Radolf2, Oleg G Chepurny3, Maritina Rouchota4, George Loudos4, Fritz Andreae2, George G Holz3, Berthold Artur Nock1, Theodosia Maina1.
Abstract
Radiolabeled gastrin analogues have been proposed for theranostics of cholecystokinin subtype 2 receptor (CCK2R)-positive cancer. Peptide radioligands based on other receptor antagonists have displayed superior pharmacokinetics and higher biosafety than agonists. Here, we present DGA1, a derivative of the nonpeptidic CCK2R antagonist Z-360 carrying an acyclic tetraamine, for [99mTc]Tc labeling. Preclinical comparison of [99mTc]Tc-DGA1 with [99mTc]Tc-DG2 (CCK2R-agonist reference) was conducted in HEK293-CCK2R/CCK2i4svR cells and mice models, qualifying [99mTc]Tc-DGA1 for further study in patients with CCK2R-positive tumors and single-photon emission computed tomography/CT.Entities:
Keywords: CCK2 receptor; CCK2R antagonist; [99mTc]Tc radiotracer; molecular imaging; tumor single-photon emission computed tomography imaging
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Year: 2020 PMID: 32568549 PMCID: PMC7429258 DOI: 10.1021/acs.molpharmaceut.0c00605
Source DB: PubMed Journal: Mol Pharm ISSN: 1543-8384 Impact factor: 4.939