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In Vivo Evaluation of Indium-111–Labeled 800CW as a Necrosis-Avid Contrast Agent

PURPOSE: Current clinical measurements for tumor treatment efficiency rely often on changes in tumor volume measured as shrinkage by CT or MRI, which become apparent after multiple lines of treatment and pose a physical and psychological burden on the patient. Detection of therapy-induced cell death...

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Autores principales: Stroet, Marcus C. M., de Blois, Erik, Stuurman, Debra C., de Ridder, Corrina M. A., Haeck, Joost, Seimbille, Yann, Mezzanotte, Laura, de Jong, Marion, Löwik, Clemens W. G. M., Panth, Kranthi M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497446/
https://www.ncbi.nlm.nih.gov/pubmed/32514888
http://dx.doi.org/10.1007/s11307-020-01511-x
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author Stroet, Marcus C. M.
de Blois, Erik
Stuurman, Debra C.
de Ridder, Corrina M. A.
Haeck, Joost
Seimbille, Yann
Mezzanotte, Laura
de Jong, Marion
Löwik, Clemens W. G. M.
Panth, Kranthi M.
author_facet Stroet, Marcus C. M.
de Blois, Erik
Stuurman, Debra C.
de Ridder, Corrina M. A.
Haeck, Joost
Seimbille, Yann
Mezzanotte, Laura
de Jong, Marion
Löwik, Clemens W. G. M.
Panth, Kranthi M.
author_sort Stroet, Marcus C. M.
collection PubMed
description PURPOSE: Current clinical measurements for tumor treatment efficiency rely often on changes in tumor volume measured as shrinkage by CT or MRI, which become apparent after multiple lines of treatment and pose a physical and psychological burden on the patient. Detection of therapy-induced cell death in the tumor can be a fast measure for treatment efficiency. However, there are no reliable clinical tools for detection of tumor necrosis. Previously, we studied the necrosis avidity of cyanine-based fluorescent dyes, which suffered long circulation times before tumor necrosis could be imaged due to low hydrophilicity. We now present the application of radiolabeled 800CW, a commercially available cyanine with high hydrophilicity, to image tumor necrosis in a mouse model. PROCEDURES: We conjugated 800CW to DOTA via a PEG linker, for labeling with single-photon emission-computed tomography isotope indium-111, yielding [(111)In]In-DOTA-PEG(4)-800CW. We then investigated specific [(111)In]In-DOTA-PEG(4)-800CW uptake by dead cells in vitro, using both fluorescence and radioactivity as detection modalities. Finally, we investigated [(111)In]In-DOTA-PEG(4)-800CW uptake into necrotic tumor regions of a 4T1 breast tumor model in mice. RESULTS: We successfully prepared a precursor and developed a reliable procedure for labeling 800CW with indium-111. We detected specific [(111)In]In-DOTA-PEG(4)-800CW uptake by dead cells, using both fluorescence and radioactivity. Albeit with a tumor uptake of only 0.37%ID/g at 6 h post injection, we were able to image tumor necrosis with a tumor to background ratio of 7:4. Fluorescence and radioactivity in cryosections from the dissected tumors were colocalized with tumor necrosis, confirmed by TUNEL staining. CONCLUSIONS: [(111)In]In-DOTA-PEG(4)-800CW can be used to image tumor necrosis in vitro and in vivo. Further research will elucidate the application of [(111)In]In-DOTA-PEG(4)-800CW or other radiolabeled hydrophilic cyanines for the detection of necrosis caused by chemotherapy or other anti-cancer therapies. This can provide valuable prognostic information in treatment of solid tumors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11307-020-01511-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-74974462020-09-29 In Vivo Evaluation of Indium-111–Labeled 800CW as a Necrosis-Avid Contrast Agent Stroet, Marcus C. M. de Blois, Erik Stuurman, Debra C. de Ridder, Corrina M. A. Haeck, Joost Seimbille, Yann Mezzanotte, Laura de Jong, Marion Löwik, Clemens W. G. M. Panth, Kranthi M. Mol Imaging Biol Research Article PURPOSE: Current clinical measurements for tumor treatment efficiency rely often on changes in tumor volume measured as shrinkage by CT or MRI, which become apparent after multiple lines of treatment and pose a physical and psychological burden on the patient. Detection of therapy-induced cell death in the tumor can be a fast measure for treatment efficiency. However, there are no reliable clinical tools for detection of tumor necrosis. Previously, we studied the necrosis avidity of cyanine-based fluorescent dyes, which suffered long circulation times before tumor necrosis could be imaged due to low hydrophilicity. We now present the application of radiolabeled 800CW, a commercially available cyanine with high hydrophilicity, to image tumor necrosis in a mouse model. PROCEDURES: We conjugated 800CW to DOTA via a PEG linker, for labeling with single-photon emission-computed tomography isotope indium-111, yielding [(111)In]In-DOTA-PEG(4)-800CW. We then investigated specific [(111)In]In-DOTA-PEG(4)-800CW uptake by dead cells in vitro, using both fluorescence and radioactivity as detection modalities. Finally, we investigated [(111)In]In-DOTA-PEG(4)-800CW uptake into necrotic tumor regions of a 4T1 breast tumor model in mice. RESULTS: We successfully prepared a precursor and developed a reliable procedure for labeling 800CW with indium-111. We detected specific [(111)In]In-DOTA-PEG(4)-800CW uptake by dead cells, using both fluorescence and radioactivity. Albeit with a tumor uptake of only 0.37%ID/g at 6 h post injection, we were able to image tumor necrosis with a tumor to background ratio of 7:4. Fluorescence and radioactivity in cryosections from the dissected tumors were colocalized with tumor necrosis, confirmed by TUNEL staining. CONCLUSIONS: [(111)In]In-DOTA-PEG(4)-800CW can be used to image tumor necrosis in vitro and in vivo. Further research will elucidate the application of [(111)In]In-DOTA-PEG(4)-800CW or other radiolabeled hydrophilic cyanines for the detection of necrosis caused by chemotherapy or other anti-cancer therapies. This can provide valuable prognostic information in treatment of solid tumors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11307-020-01511-x) contains supplementary material, which is available to authorized users. Springer International Publishing 2020-06-08 2020 /pmc/articles/PMC7497446/ /pubmed/32514888 http://dx.doi.org/10.1007/s11307-020-01511-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Stroet, Marcus C. M.
de Blois, Erik
Stuurman, Debra C.
de Ridder, Corrina M. A.
Haeck, Joost
Seimbille, Yann
Mezzanotte, Laura
de Jong, Marion
Löwik, Clemens W. G. M.
Panth, Kranthi M.
In Vivo Evaluation of Indium-111–Labeled 800CW as a Necrosis-Avid Contrast Agent
title In Vivo Evaluation of Indium-111–Labeled 800CW as a Necrosis-Avid Contrast Agent
title_full In Vivo Evaluation of Indium-111–Labeled 800CW as a Necrosis-Avid Contrast Agent
title_fullStr In Vivo Evaluation of Indium-111–Labeled 800CW as a Necrosis-Avid Contrast Agent
title_full_unstemmed In Vivo Evaluation of Indium-111–Labeled 800CW as a Necrosis-Avid Contrast Agent
title_short In Vivo Evaluation of Indium-111–Labeled 800CW as a Necrosis-Avid Contrast Agent
title_sort in vivo evaluation of indium-111–labeled 800cw as a necrosis-avid contrast agent
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497446/
https://www.ncbi.nlm.nih.gov/pubmed/32514888
http://dx.doi.org/10.1007/s11307-020-01511-x
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