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Synergism of peptide receptor-targeted Auger electron radiation therapy with anti-angiogenic compounds in a mouse model of neuroendocrine tumors

BACKGROUND: Neuroendocrine tumors are well vascularized and express specific cell surface markers, such as somatostatin receptors and the glucagon-like peptide-1 receptor (GLP-1R). Using the Rip1Tag2 transgenic mouse model of pancreatic neuroendocrine tumors (pNET), we have investigated the potentia...

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Autores principales: Wicki, Andreas, Wild, Damian, Prêtre, Vincent, Mansi, Rosalba, Orleth, Annette, Reubi, Jean-Claude, Rochlitz, Christoph, Mamot, Christoph, Mäcke, Helmut R, Christofori, Gerhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937006/
https://www.ncbi.nlm.nih.gov/pubmed/24528513
http://dx.doi.org/10.1186/2191-219X-4-9
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author Wicki, Andreas
Wild, Damian
Prêtre, Vincent
Mansi, Rosalba
Orleth, Annette
Reubi, Jean-Claude
Rochlitz, Christoph
Mamot, Christoph
Mäcke, Helmut R
Christofori, Gerhard
author_facet Wicki, Andreas
Wild, Damian
Prêtre, Vincent
Mansi, Rosalba
Orleth, Annette
Reubi, Jean-Claude
Rochlitz, Christoph
Mamot, Christoph
Mäcke, Helmut R
Christofori, Gerhard
author_sort Wicki, Andreas
collection PubMed
description BACKGROUND: Neuroendocrine tumors are well vascularized and express specific cell surface markers, such as somatostatin receptors and the glucagon-like peptide-1 receptor (GLP-1R). Using the Rip1Tag2 transgenic mouse model of pancreatic neuroendocrine tumors (pNET), we have investigated the potential benefit of a combination of anti-angiogenic treatment with targeted internal radiotherapy. METHODS: [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4, a radiopeptide that selectively binds to GLP-1R expressed on insulinoma and other neuroendocrine tumor cells, was co-administered with oral vatalanib (an inhibitor of vascular endothelial growth factor receptors (VEGFR)) or imatinib (a c-kit/PDGFR inhibitor). The control groups included single-agent kinase inhibitor treatments and [Lys(40)(Ahx-DTPA-(nat)In)NH(2)]-exendin-4 monotherapy. For biodistribution, Rip1Tag2 mice were pre-treated with oral vatalanib or imatinib for 0, 3, 5, or 7 days at a dose of 100 mg/kg. Subsequently, [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4 was administered i.v., and the biodistribution was assessed after 4 h. For therapy, the mice were injected with 1.1 MBq [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4 and treated with vatalanib or imatinib 100 mg/kg orally for another 7 days. Tumor volume, tumor cell apoptosis and proliferation, and microvessel density were quantified. RESULTS: Combination of [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4 and vatalanib was significantly more effective than single treatments (p < 0.05) and reduced the tumor volume by 97% in the absence of organ damage. The pre-treatment of mice with vatalanib led to a reduction in the tumor uptake of [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4, indicating that concomitant administration of vatalanib and the radiopeptide was the best approach. Imatinib did not show a synergistic effect with [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4. CONCLUSION: The combination of 1.1 MBq of [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4 with 100 mg/kg vatalanib had the same effect on a neuroendocrine tumor as the injection of 28 MBq of the radiopeptide alone but without any apparent side effects, such as radiation damage of the kidneys.
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spelling pubmed-39370062014-03-10 Synergism of peptide receptor-targeted Auger electron radiation therapy with anti-angiogenic compounds in a mouse model of neuroendocrine tumors Wicki, Andreas Wild, Damian Prêtre, Vincent Mansi, Rosalba Orleth, Annette Reubi, Jean-Claude Rochlitz, Christoph Mamot, Christoph Mäcke, Helmut R Christofori, Gerhard EJNMMI Res Original Research BACKGROUND: Neuroendocrine tumors are well vascularized and express specific cell surface markers, such as somatostatin receptors and the glucagon-like peptide-1 receptor (GLP-1R). Using the Rip1Tag2 transgenic mouse model of pancreatic neuroendocrine tumors (pNET), we have investigated the potential benefit of a combination of anti-angiogenic treatment with targeted internal radiotherapy. METHODS: [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4, a radiopeptide that selectively binds to GLP-1R expressed on insulinoma and other neuroendocrine tumor cells, was co-administered with oral vatalanib (an inhibitor of vascular endothelial growth factor receptors (VEGFR)) or imatinib (a c-kit/PDGFR inhibitor). The control groups included single-agent kinase inhibitor treatments and [Lys(40)(Ahx-DTPA-(nat)In)NH(2)]-exendin-4 monotherapy. For biodistribution, Rip1Tag2 mice were pre-treated with oral vatalanib or imatinib for 0, 3, 5, or 7 days at a dose of 100 mg/kg. Subsequently, [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4 was administered i.v., and the biodistribution was assessed after 4 h. For therapy, the mice were injected with 1.1 MBq [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4 and treated with vatalanib or imatinib 100 mg/kg orally for another 7 days. Tumor volume, tumor cell apoptosis and proliferation, and microvessel density were quantified. RESULTS: Combination of [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4 and vatalanib was significantly more effective than single treatments (p < 0.05) and reduced the tumor volume by 97% in the absence of organ damage. The pre-treatment of mice with vatalanib led to a reduction in the tumor uptake of [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4, indicating that concomitant administration of vatalanib and the radiopeptide was the best approach. Imatinib did not show a synergistic effect with [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4. CONCLUSION: The combination of 1.1 MBq of [Lys(40)(Ahx-DTPA-(111)In)NH(2)]-exendin-4 with 100 mg/kg vatalanib had the same effect on a neuroendocrine tumor as the injection of 28 MBq of the radiopeptide alone but without any apparent side effects, such as radiation damage of the kidneys. Springer 2014-02-16 /pmc/articles/PMC3937006/ /pubmed/24528513 http://dx.doi.org/10.1186/2191-219X-4-9 Text en Copyright © 2014 Wicki et al.; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Original Research
Wicki, Andreas
Wild, Damian
Prêtre, Vincent
Mansi, Rosalba
Orleth, Annette
Reubi, Jean-Claude
Rochlitz, Christoph
Mamot, Christoph
Mäcke, Helmut R
Christofori, Gerhard
Synergism of peptide receptor-targeted Auger electron radiation therapy with anti-angiogenic compounds in a mouse model of neuroendocrine tumors
title Synergism of peptide receptor-targeted Auger electron radiation therapy with anti-angiogenic compounds in a mouse model of neuroendocrine tumors
title_full Synergism of peptide receptor-targeted Auger electron radiation therapy with anti-angiogenic compounds in a mouse model of neuroendocrine tumors
title_fullStr Synergism of peptide receptor-targeted Auger electron radiation therapy with anti-angiogenic compounds in a mouse model of neuroendocrine tumors
title_full_unstemmed Synergism of peptide receptor-targeted Auger electron radiation therapy with anti-angiogenic compounds in a mouse model of neuroendocrine tumors
title_short Synergism of peptide receptor-targeted Auger electron radiation therapy with anti-angiogenic compounds in a mouse model of neuroendocrine tumors
title_sort synergism of peptide receptor-targeted auger electron radiation therapy with anti-angiogenic compounds in a mouse model of neuroendocrine tumors
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937006/
https://www.ncbi.nlm.nih.gov/pubmed/24528513
http://dx.doi.org/10.1186/2191-219X-4-9
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