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Multi-Modal PET and MR Imaging in the Hen’s Egg Test-Chorioallantoic Membrane (HET-CAM) Model for Initial In Vivo Testing of Target-Specific Radioligands

Authors :
Christoph Solbach
Hao Li
Alireza Abaei
Ambros J. Beer
Gordon Winter
Mika Lindén
Gerhard Glatting
AB Koch
Volker Rasche
J Löffler
European Union (EU)
Horizon 2020
Source :
Cancers, Volume 12, Issue 5, Cancers, Vol 12, Iss 1248, p 1248 (2020)
Publication Year :
2020
Publisher :
MDPI AG, 2020.

Abstract

The validation of novel target-specific radioligands requires animal experiments mostly using mice with xenografts. A pre-selection based on a simpler in vivo model would allow to reduce the number of animal experiments, in accordance with the 3Rs principles (reduction, replacement, refinement). In this respect, the chick embryo or hen&rsquo<br />s egg test&ndash<br />chorioallantoic membrane (HET-CAM) model is of special interest, as it is not considered an animal until day 17. Thus, we evaluated the feasibility of quantitative analysis of target-specific radiotracer accumulation in xenografts using the HET-CAM model and combined positron emission tomography (PET) and magnetic resonance imaging (MRI). For proof-of-principle we used established prostate-specific membrane antigen (PSMA)-positive and PSMA-negative prostate cancer xenografts and the clinically widely used PSMA-specific PET-tracer [68Ga]Ga-PSMA-11. Tracer accumulation was quantified by PET and tumor volumes measured with MRI (n = 42). Moreover, gamma-counter analysis of radiotracer accumulation was done ex-vivo. A three- to five-fold higher ligand accumulation in the PSMA-positive tumors compared to the PSMA-negative tumors was demonstrated. This proof-of-principle study shows the general feasibility of the HET-CAM xenograft model for target-specific imaging with PET and MRI. The ultimate value for characterization of novel target-specific radioligands now has to be validated in comparison to mouse xenograft experiments.

Details

ISSN :
20726694
Volume :
12
Database :
OpenAIRE
Journal :
Cancers
Accession number :
edsair.doi.dedup.....3931a65adcbd649f97f7446eb581580c
Full Text :
https://doi.org/10.3390/cancers12051248