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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer
2014
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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. |
format | Online Article Text |
id | pubmed-3937006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer |
record_format | MEDLINE/PubMed |
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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