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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...

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Autores principales: Förnvik, Karolina, Ahlstedt, Jonatan, Osther, Kurt, Salford, Leif G., Redebrandt, Henrietta Nittby
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
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.
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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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