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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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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
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author Latgé, Adrien
Boisson, Frédéric
Ouadi, Ali
Averous, Gerlinde
Thomas, Lionel
Imperiale, Alessio
Brasse, David
author_facet Latgé, Adrien
Boisson, Frédéric
Ouadi, Ali
Averous, Gerlinde
Thomas, Lionel
Imperiale, Alessio
Brasse, David
author_sort Latgé, Adrien
collection PubMed
description (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.
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spelling pubmed-93695692022-08-12 (64)CuCl(2) PET Imaging of 4T1-Related Allograft of Triple-Negative Breast Cancer in Mice Latgé, Adrien Boisson, Frédéric Ouadi, Ali Averous, Gerlinde Thomas, Lionel Imperiale, Alessio Brasse, David Molecules Article (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. MDPI 2022-07-29 /pmc/articles/PMC9369569/ /pubmed/35956819 http://dx.doi.org/10.3390/molecules27154869 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Latgé, Adrien
Boisson, Frédéric
Ouadi, Ali
Averous, Gerlinde
Thomas, Lionel
Imperiale, Alessio
Brasse, David
(64)CuCl(2) PET Imaging of 4T1-Related Allograft of Triple-Negative Breast Cancer in Mice
title (64)CuCl(2) PET Imaging of 4T1-Related Allograft of Triple-Negative Breast Cancer in Mice
title_full (64)CuCl(2) PET Imaging of 4T1-Related Allograft of Triple-Negative Breast Cancer in Mice
title_fullStr (64)CuCl(2) PET Imaging of 4T1-Related Allograft of Triple-Negative Breast Cancer in Mice
title_full_unstemmed (64)CuCl(2) PET Imaging of 4T1-Related Allograft of Triple-Negative Breast Cancer in Mice
title_short (64)CuCl(2) PET Imaging of 4T1-Related Allograft of Triple-Negative Breast Cancer in Mice
title_sort (64)cucl(2) pet imaging of 4t1-related allograft of triple-negative breast cancer in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369569/
https://www.ncbi.nlm.nih.gov/pubmed/35956819
http://dx.doi.org/10.3390/molecules27154869
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