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  3. [111In-DOTA]LTT-SS28, a first pansomatostatin radioligand for in vivo targeting of somatostatin receptor-positive tumors

[111In-DOTA]LTT-SS28, a first pansomatostatin radioligand for in vivo targeting of somatostatin receptor-positive tumors

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DOI
10.7892/boris.66500
Publisher DOI
10.1021/jm500581d
PubMed ID
25007399
Abstract
Radiolabeled pansomatostatin-like analogues are expected to enhance the diagnostic sensitivity and to expand the clinical indications of currently applied sst2-specific radioligands. In this study, we present the somatostatin mimic [DOTA]LTT-SS28 {[(DOTA)Ser1,Leu8,D-Trp22,Tyr25]SS28} and its 111In radioligand. [DOTA]LTT-SS28 exhibited a pansomatostatin-like profile binding with high affinity to all five hsst1-hsst5 subtypes (IC50 values in the lower nanomolar range). Furthermore, [DOTA]LTT-SS28 behaved as an agonist at hsst2, hsst3, and hsst5, efficiently stimulating internalization of the three receptor subtypes. Radioligand [111In-DOTA]LTT-SS28 showed good stability in the mouse bloodstream. It displayed strong and specific uptake in AR42J tumors 4 h postinjection (9.3±1.6% ID/g vs 0.3±0.0% ID/g during sst2 blockade) in mice. Significant and specific uptake was also observed in HEK293-hsst2-, HEK293-hsst3-, and HEK293-hsst5-expressing tumors (4.43±1.5, 4.88±1.1, and <3% ID/g, respectively, with values of <0.5% ID/g during receptor blockade). In conclusion, the somatostatin mimic [111In-DOTA]LTT-SS28 specifically localizes in sst2-, sst3-, and sst5-expressing xenografts in mice showing promise for multi-sst1-sst5 targeted tumor imaging.
Date Issued
2014-08-14
Publication Type
Article
Subject(s)
500 Science > 570 Life sciences; biology
600 Technology > 610 Medicine & health
Language(s)
en
Author(s)
Maina, Theodosia
Cescato, Renzo  
Departement Klinische Forschung, Forschungsgruppe Klinische Radiopharmazie  
Waser, Beatrice  
Institut für Pathologie  
Tatsi, Aikaterini
Kaloudi, Aikaterini
Krenning, Eric P
de Jong, Marion
Nock, Berthold A
Reubi-Kattenbusch, Jean-Claude  
Institut für Pathologie  
Additional Credits
Institut für Pathologie  
Departement Klinische Forschung, Forschungsgruppe Klinische Radiopharmazie  
Journal
Journal of medicinal chemistry
Publisher
American Chemical Society
ISSN
0022-2623
Access(Rights)
restricted
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