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Anti-C1-inactivator treatment of glioblastoma
PURPOSE: Glioblastoma multiforme (GBM) or astrocytoma grade IV is the most common type of primary brain tumor in adults. In the present study, we investigate the role of the complement system in the glioblastoma situation in an experimental model, since we have previously been able to show a blockad...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324776/ https://www.ncbi.nlm.nih.gov/pubmed/30647842 http://dx.doi.org/10.18632/oncotarget.26456 |
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author | Förnvik, Karolina Ahlstedt, Jonatan Osther, Kurt Salford, Leif G. Redebrandt, Henrietta Nittby |
author_facet | Förnvik, Karolina Ahlstedt, Jonatan Osther, Kurt Salford, Leif G. Redebrandt, Henrietta Nittby |
author_sort | Förnvik, Karolina |
collection | PubMed |
description | PURPOSE: Glioblastoma multiforme (GBM) or astrocytoma grade IV is the most common type of primary brain tumor in adults. In the present study, we investigate the role of the complement system in the glioblastoma situation in an experimental model, since we have previously been able to show a blockade of this system in the glioblastoma setting. TECHNIQUE AND RESULTS: A GFP-positive glioblastoma cell line was used to induce glioblastomas subcutaneously in rats (n=42). Antibodies against C1-Inactivator (C1-IA) were used to try to re-activate the complement system. We were able to demonstrate an increased survival in rats treated with anti-C1-IA with an intratumoral route, and we could establish the same the results in a second series. Serum analyses revealed decreased levels of IL-1b and GM-CSF in animals 24 days after tumor cell inoculation in the anti-C1-IA group when compared to controls. Immunohistochemistry revealed decreased expression of C1-IA following treatment. INTERPRETATION: These results are in line with our previous work showing an upregulation of C1-IA, which is able to block the classical complement pathway, in glioblastomas. Treatment with antibodies against C1-IA seems to be beneficial in the glioblastoma situation, and no side effects could be seen in our experiments. |
format | Online Article Text |
id | pubmed-6324776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-63247762019-01-15 Anti-C1-inactivator treatment of glioblastoma Förnvik, Karolina Ahlstedt, Jonatan Osther, Kurt Salford, Leif G. Redebrandt, Henrietta Nittby Oncotarget Research Paper PURPOSE: Glioblastoma multiforme (GBM) or astrocytoma grade IV is the most common type of primary brain tumor in adults. In the present study, we investigate the role of the complement system in the glioblastoma situation in an experimental model, since we have previously been able to show a blockade of this system in the glioblastoma setting. TECHNIQUE AND RESULTS: A GFP-positive glioblastoma cell line was used to induce glioblastomas subcutaneously in rats (n=42). Antibodies against C1-Inactivator (C1-IA) were used to try to re-activate the complement system. We were able to demonstrate an increased survival in rats treated with anti-C1-IA with an intratumoral route, and we could establish the same the results in a second series. Serum analyses revealed decreased levels of IL-1b and GM-CSF in animals 24 days after tumor cell inoculation in the anti-C1-IA group when compared to controls. Immunohistochemistry revealed decreased expression of C1-IA following treatment. INTERPRETATION: These results are in line with our previous work showing an upregulation of C1-IA, which is able to block the classical complement pathway, in glioblastomas. Treatment with antibodies against C1-IA seems to be beneficial in the glioblastoma situation, and no side effects could be seen in our experiments. Impact Journals LLC 2018-12-21 /pmc/articles/PMC6324776/ /pubmed/30647842 http://dx.doi.org/10.18632/oncotarget.26456 Text en Copyright: © 2018 Förnvik et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Förnvik, Karolina Ahlstedt, Jonatan Osther, Kurt Salford, Leif G. Redebrandt, Henrietta Nittby Anti-C1-inactivator treatment of glioblastoma |
title | Anti-C1-inactivator treatment of glioblastoma |
title_full | Anti-C1-inactivator treatment of glioblastoma |
title_fullStr | Anti-C1-inactivator treatment of glioblastoma |
title_full_unstemmed | Anti-C1-inactivator treatment of glioblastoma |
title_short | Anti-C1-inactivator treatment of glioblastoma |
title_sort | anti-c1-inactivator treatment of glioblastoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324776/ https://www.ncbi.nlm.nih.gov/pubmed/30647842 http://dx.doi.org/10.18632/oncotarget.26456 |
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