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(64)CuCl(2) PET Imaging of 4T1-Related Allograft of Triple-Negative Breast Cancer in Mice

(64)CuCl(2) is an economic radiotracer for oncologic PET investigations. In the present study, we characterized the uptake of (64)CuCl(2) in vivo by µPET/CT in an allograft 4T1-related mouse model (BALB/c) of advanced breast cancer. (18)F-FDG was used as a comparator. Twenty-two animals were imaged...

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Detalles Bibliográficos
Autores principales: Latgé, Adrien, Boisson, Frédéric, Ouadi, Ali, Averous, Gerlinde, Thomas, Lionel, Imperiale, Alessio, Brasse, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369569/
https://www.ncbi.nlm.nih.gov/pubmed/35956819
http://dx.doi.org/10.3390/molecules27154869
Descripción
Sumario:(64)CuCl(2) is an economic radiotracer for oncologic PET investigations. In the present study, we characterized the uptake of (64)CuCl(2) in vivo by µPET/CT in an allograft 4T1-related mouse model (BALB/c) of advanced breast cancer. (18)F-FDG was used as a comparator. Twenty-two animals were imaged 7–9 days following 4T1-cell implantation inside mammary glands. Dynamic (64)CuCl(2) µPET/CT acquisition or iterative static images up to 8 h p.i. were performed. Animal biodistribution and tumor uptake were first evaluated in vivo by µPET analysis and then assessed on tissue specimens. Concerning (18)F-FDG µPET, a static acquisition was performed at 15 min and 60 min p.i. Tumor (64)CuCl(2) accumulation increased from 5 min to 4 h p.i., reaching a maximum value of 5.0 ± 0.20 %ID/g. Liver, brain, and muscle (64)CuCl(2) accumulation was stable over time. The tumor-to-muscle ratio remained stable from 1 to 8 h p.i., ranging from 3.0 to 3.7. Ex vivo data were consistent with in vivo estimations. The (18)F-FDG tumor accumulation was 8.82 ± 1.03 %ID/g, and the tumor-to-muscle ratio was 4.54 ± 1.11. (64)CuCl(2) PET/CT provides good characterization of the 4T1-related breast cancer model and allows for exploration of non-glycolytic cellular pathways potentially of interest for theragnostic strategies.