dc.contributor.author
Erdmann, Sarah
dc.contributor.author
Niederstadt, Lars
dc.contributor.author
Koziolek, Eva Jolanthe
dc.contributor.author
Gómez, Juan Daniel Castillo
dc.contributor.author
Prasad, Sonal
dc.contributor.author
Wagener, Asja
dc.contributor.author
Hacht, Jan Lennart von
dc.contributor.author
Reinicke, Sandy
dc.contributor.author
Exner, Samantha
dc.contributor.author
Bandholtz, Sebastian
dc.contributor.author
Beindorff, Nicola
dc.contributor.author
Brenner, Winfried
dc.contributor.author
Grötzinger, Carsten
dc.date.accessioned
2019-12-12T09:05:37Z
dc.date.available
2019-12-12T09:05:37Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/26100
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-25860
dc.description.abstract
Background: Molecular targeting remains to be a promising approach in oncology. Overexpression of G protein-coupled receptors (GPCRs) in human cancer is offering a powerful opportunity for tumor-selective imaging and treatment employing nuclear medicine. We utilized novel chemerin-based peptide conjugates for chemokine-like receptor 1 (CMKLR1) targeting in a breast cancer xenograft model. Methods: By conjugation with the chelator 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA), we obtained a family of five highly specific, high-affinity tracers for hybrid positron emission tomography/magnetic resonance (PET/MR) imaging. A xenograft model with target-positive DU4475 and negative A549 tumors in immunodeficient nude mice enabled CMKLR1-specific imaging in vivo. We acquired small animal PET/MR images, assessed biodistribution by ex vivo measurements and investigated the tracer specificity by blocking experiments. Results: Five CMKLR1-targeting peptide tracers demonstrated high biological activity and affinity in vitro with EC50 and IC50 values below 2 nM. Our target-positive (DU4475) and target-negative (A549) xenograft model could be validated by ex vivo analysis of CMKLR1 expression and binding. After preliminary PET imaging, the three most promising tracers [68Ga]Ga-DOTA-AHX-CG34, [68Ga]Ga-DOTA-KCap-CG34 and [68Ga]Ga-DOTA-ADX-CG34 with best tumor uptake were further analyzed. Hybrid PET/MR imaging along with concomitant biodistribution studies revealed distinct CMKLR1-specific uptake (5.1% IA/g, 3.3% IA/g and 6.2% IA/g 1 h post-injection) of our targeted tracers in DU4475 tumor tissue. In addition, tumor uptake was blocked by excess of unlabeled peptide (6.4-fold, 5.5-fold and 3.4-fold 1 h post-injection), further confirming CMKLR1 specificity. Out of five tracers, we identified these three tracers with moderate, balanced hydrophilicity to be the most potent in receptor-mediated tumor targeting. Conclusion: We demonstrated the applicability of 68Ga-labeled peptide tracers by visualizing CMKLR1-positive breast cancer xenografts in PET/MR imaging, paving the way for developing them into theranostics for tumor treatment.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Chemokine-like receptor 1
en
dc.subject
Tumor targeting
en
dc.subject
breast cancer
en
dc.subject
peptide ligand
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
CMKLR1-targeting peptide tracers for PET/MR imaging of breast cancer
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.7150/thno.34857
dcterms.bibliographicCitation.journaltitle
Theranostics
dcterms.bibliographicCitation.number
22
dcterms.bibliographicCitation.originalpublishername
Ivyspring International Publisher
dcterms.bibliographicCitation.pagestart
6719
dcterms.bibliographicCitation.pageend
6733
dcterms.bibliographicCitation.volume
9
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
31588246
dcterms.isPartOf.eissn
1838-7640