In vivo and in vitro characterization of CCK8 bearing a histidine‐based chelator labeled with 99m Tc‐tricarbonyl

• Published in: Peptide Science Vol. 90; no. 5; pp. 707 - 712
• Main Authors: D'Andrea, Luca D., Testa, Irma, Panico, MariaRosaria, Di Stasi, Rossella, Caracò, Corradina, Tarallo, Laura, Arra, Claudio, Barbieri, Antonio, Romanelli, Alessandra, Aloj, Luigi
• Format: Journal Article
• Language: English
• Published: 01.01.2008
• ISSN: 0006-3525
• DOI: 10.1002/bip.21041

Abstract The development of receptor targeting radiolabeled ligands has gained much interest in recent years for diagnostic and therapeutic applications in nuclear medicine. Cholecystokinin (CCK) receptors have been shown to be overexpressed in a subset of neuroendocrine and other tumors. We are evaluating binding and biodistribution properties of a CCK8 peptide derivative labeled with 99m Tc(I)‐tricarbonyl. The CCK8 peptide was modified at its N‐terminus by adding to its N‐terminus two lysine–histidine modules (KH), where histidine is coupled to the side chain of the lysine ((KH) 2 ‐CCK8). 99m Tc(I)‐tricarbonyl was generated with the IsoLink™ kit. A431 cells stably transfected with a cDNA encoding for the human CCK2 receptor were utilized to determine binding affinity, internalization, and retention of the labeled peptide, in comparison with wild‐type A431 cells. A nude mouse tumor model was obtained by generating A431‐CCK2R and A431‐control tumors in opposite flanks of the animals. High specific activity labeling with 99m Tc was achieved. In A431‐CCK2R cells, specific saturable binding was observed as well as evident internalization of the radiolabeled peptide after binding. Biodistribution experiments showed rapid, specific localization of (KH) 2 ‐CCK8 on A431‐CCK2R xenografts compared with control tumors, although absolute uptake values were not markedly higher compared with background activity. Clearance of unbound radioactivity was both urinary and hepatobiliary. In imaging experiments, while targeting to CCK2R positive tumors could be appreciated, there was poor contrast between target and nontarget areas. (KH) 2 ‐CCK8 shows adequate in vitro and in vivo properties for CCK2R targeting although improvement of biodistribution warrant further development. © 2008 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 90: 707–712, 2008. This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at biopolymers@wiley.com