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The novel sigma-2 receptor ligand SW43 stabilizes pancreas cancer progression in combination with gemcitabine
BACKGROUND: Sigma-2 receptors are over-expressed in proliferating cancer cells, making an attractive target for the targeted treatment of pancreatic cancer. In this study, we investigated the role of the novel sigma-2 receptor ligand SW43 to induce apoptosis and augment standard chemotherapy. RESULT...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3106998/ https://www.ncbi.nlm.nih.gov/pubmed/21092190 http://dx.doi.org/10.1186/1476-4598-9-298 |
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author | Hornick, John R Xu, Jinbin Vangveravong, Suwanna Tu, Zhude Mitchem, Jonathan B Spitzer, Dirk Goedegebuure, Peter Mach, Robert H Hawkins, William G |
author_facet | Hornick, John R Xu, Jinbin Vangveravong, Suwanna Tu, Zhude Mitchem, Jonathan B Spitzer, Dirk Goedegebuure, Peter Mach, Robert H Hawkins, William G |
author_sort | Hornick, John R |
collection | PubMed |
description | BACKGROUND: Sigma-2 receptors are over-expressed in proliferating cancer cells, making an attractive target for the targeted treatment of pancreatic cancer. In this study, we investigated the role of the novel sigma-2 receptor ligand SW43 to induce apoptosis and augment standard chemotherapy. RESULTS: The binding affinity for sigma-2 ligands is high in pancreas cancer, and they induce apoptosis with a rank order of SV119 < SW43 < SRM in vitro. Combining these compounds with gemcitabine further increased apoptosis and decreased viability. Our in vivo model showed that sigma-2 ligand treatment decreased tumor volume to the same extent as gemcitabine. However, SW43 combination treatment with gemcitabine was superior to the other compounds and resulted in stabilization of tumor volume during treatment, with minimal toxicities. CONCLUSIONS: This study shows that the sigma-2 ligand SW43 has the greatest capacity to augment gemcitabine in a pre-clinical model of pancreas cancer and has provided us with the rationale to move this compound forward with clinical investigations for patients with pancreatic cancer. |
format | Online Article Text |
id | pubmed-3106998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31069982011-06-06 The novel sigma-2 receptor ligand SW43 stabilizes pancreas cancer progression in combination with gemcitabine Hornick, John R Xu, Jinbin Vangveravong, Suwanna Tu, Zhude Mitchem, Jonathan B Spitzer, Dirk Goedegebuure, Peter Mach, Robert H Hawkins, William G Mol Cancer Research BACKGROUND: Sigma-2 receptors are over-expressed in proliferating cancer cells, making an attractive target for the targeted treatment of pancreatic cancer. In this study, we investigated the role of the novel sigma-2 receptor ligand SW43 to induce apoptosis and augment standard chemotherapy. RESULTS: The binding affinity for sigma-2 ligands is high in pancreas cancer, and they induce apoptosis with a rank order of SV119 < SW43 < SRM in vitro. Combining these compounds with gemcitabine further increased apoptosis and decreased viability. Our in vivo model showed that sigma-2 ligand treatment decreased tumor volume to the same extent as gemcitabine. However, SW43 combination treatment with gemcitabine was superior to the other compounds and resulted in stabilization of tumor volume during treatment, with minimal toxicities. CONCLUSIONS: This study shows that the sigma-2 ligand SW43 has the greatest capacity to augment gemcitabine in a pre-clinical model of pancreas cancer and has provided us with the rationale to move this compound forward with clinical investigations for patients with pancreatic cancer. BioMed Central 2010-11-22 /pmc/articles/PMC3106998/ /pubmed/21092190 http://dx.doi.org/10.1186/1476-4598-9-298 Text en Copyright ©2010 Hornick et al; licensee BioMed Central Ltd. 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 cited. |
spellingShingle | Research Hornick, John R Xu, Jinbin Vangveravong, Suwanna Tu, Zhude Mitchem, Jonathan B Spitzer, Dirk Goedegebuure, Peter Mach, Robert H Hawkins, William G The novel sigma-2 receptor ligand SW43 stabilizes pancreas cancer progression in combination with gemcitabine |
title | The novel sigma-2 receptor ligand SW43 stabilizes pancreas cancer progression in combination with gemcitabine |
title_full | The novel sigma-2 receptor ligand SW43 stabilizes pancreas cancer progression in combination with gemcitabine |
title_fullStr | The novel sigma-2 receptor ligand SW43 stabilizes pancreas cancer progression in combination with gemcitabine |
title_full_unstemmed | The novel sigma-2 receptor ligand SW43 stabilizes pancreas cancer progression in combination with gemcitabine |
title_short | The novel sigma-2 receptor ligand SW43 stabilizes pancreas cancer progression in combination with gemcitabine |
title_sort | novel sigma-2 receptor ligand sw43 stabilizes pancreas cancer progression in combination with gemcitabine |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3106998/ https://www.ncbi.nlm.nih.gov/pubmed/21092190 http://dx.doi.org/10.1186/1476-4598-9-298 |
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