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(89)Zr-Labeled AR20.5: A MUC1-Targeting ImmunoPET Probe
High expression levels of the tumor-associated antigen MUC1 have been correlated with tumor aggressiveness, poor response to therapy, and poor survival in several tumor types, including breast, pancreatic, and epithelial ovarian cancer. Herein, we report the synthesis, characterization, and in vivo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287814/ https://www.ncbi.nlm.nih.gov/pubmed/32429033 http://dx.doi.org/10.3390/molecules25102315 |
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author | Fung, Kimberly Vivier, Delphine Keinänen, Outi Sarbisheh, Elaheh Khozeimeh Price, Eric W. Zeglis, Brian M. |
author_facet | Fung, Kimberly Vivier, Delphine Keinänen, Outi Sarbisheh, Elaheh Khozeimeh Price, Eric W. Zeglis, Brian M. |
author_sort | Fung, Kimberly |
collection | PubMed |
description | High expression levels of the tumor-associated antigen MUC1 have been correlated with tumor aggressiveness, poor response to therapy, and poor survival in several tumor types, including breast, pancreatic, and epithelial ovarian cancer. Herein, we report the synthesis, characterization, and in vivo evaluation of a novel radioimmunoconjugate for the immuno-positron emission tomography (immunoPET) imaging of MUC1 expression based on the AR20.5 antibody. To this end, we modified AR20.5 with the chelator desferrioxamine (DFO) and labeled it with the positron-emitting radiometal zirconium-89 (t(1/2) ~3.3 d) to produce [(89)Zr]Zr-DFO-AR20.5. In subsequent in vivo experiments in athymic nude mice bearing subcutaneous MUC1-expressing ovarian cancer xenografts, [(89)Zr]Zr-DFO-AR20.5 clearly delineated tumor tissue, producing a tumoral activity concentration of 19.1 ± 6.4 percent injected dose per gram (%ID/g) at 120 h post-injection and a tumor-to-muscle activity concentration ratio of 42.4 ± 10.6 at the same time point. Additional PET imaging experiments in mice bearing orthotopic MUC1-expressing ovarian cancer xenografts likewise demonstrated that [(89)Zr]Zr-DFO-AR20.5 enables the visualization of tumor tissue—including metastatic lesions—with promising tumor-to-background contrast. |
format | Online Article Text |
id | pubmed-7287814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72878142020-06-15 (89)Zr-Labeled AR20.5: A MUC1-Targeting ImmunoPET Probe Fung, Kimberly Vivier, Delphine Keinänen, Outi Sarbisheh, Elaheh Khozeimeh Price, Eric W. Zeglis, Brian M. Molecules Article High expression levels of the tumor-associated antigen MUC1 have been correlated with tumor aggressiveness, poor response to therapy, and poor survival in several tumor types, including breast, pancreatic, and epithelial ovarian cancer. Herein, we report the synthesis, characterization, and in vivo evaluation of a novel radioimmunoconjugate for the immuno-positron emission tomography (immunoPET) imaging of MUC1 expression based on the AR20.5 antibody. To this end, we modified AR20.5 with the chelator desferrioxamine (DFO) and labeled it with the positron-emitting radiometal zirconium-89 (t(1/2) ~3.3 d) to produce [(89)Zr]Zr-DFO-AR20.5. In subsequent in vivo experiments in athymic nude mice bearing subcutaneous MUC1-expressing ovarian cancer xenografts, [(89)Zr]Zr-DFO-AR20.5 clearly delineated tumor tissue, producing a tumoral activity concentration of 19.1 ± 6.4 percent injected dose per gram (%ID/g) at 120 h post-injection and a tumor-to-muscle activity concentration ratio of 42.4 ± 10.6 at the same time point. Additional PET imaging experiments in mice bearing orthotopic MUC1-expressing ovarian cancer xenografts likewise demonstrated that [(89)Zr]Zr-DFO-AR20.5 enables the visualization of tumor tissue—including metastatic lesions—with promising tumor-to-background contrast. MDPI 2020-05-15 /pmc/articles/PMC7287814/ /pubmed/32429033 http://dx.doi.org/10.3390/molecules25102315 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fung, Kimberly Vivier, Delphine Keinänen, Outi Sarbisheh, Elaheh Khozeimeh Price, Eric W. Zeglis, Brian M. (89)Zr-Labeled AR20.5: A MUC1-Targeting ImmunoPET Probe |
title | (89)Zr-Labeled AR20.5: A MUC1-Targeting ImmunoPET Probe |
title_full | (89)Zr-Labeled AR20.5: A MUC1-Targeting ImmunoPET Probe |
title_fullStr | (89)Zr-Labeled AR20.5: A MUC1-Targeting ImmunoPET Probe |
title_full_unstemmed | (89)Zr-Labeled AR20.5: A MUC1-Targeting ImmunoPET Probe |
title_short | (89)Zr-Labeled AR20.5: A MUC1-Targeting ImmunoPET Probe |
title_sort | (89)zr-labeled ar20.5: a muc1-targeting immunopet probe |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287814/ https://www.ncbi.nlm.nih.gov/pubmed/32429033 http://dx.doi.org/10.3390/molecules25102315 |
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