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Adjuvant therapeutic potential of tonabersat in the standard treatment of glioblastoma: A preclinical F98 glioblastoma rat model study

PURPOSE: Even with an optimal treatment protocol, the median survival of glioblastoma (GB) patients is only 12–15 months. Hence, there is need for novel effective therapies that improve survival outcomes. Recent evidence suggests an important role for connexin (Cx) proteins (especially Cx43) in the...

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Autores principales: De Meulenaere, Valerie, Bonte, Ellen, Verhoeven, Jeroen, Kalala Okito, Jean-Pierre, Pieters, Leen, Vral, Anne, De Wever, Olivier, Leybaert, Luc, Goethals, Ingeborg, Vanhove, Christian, Descamps, Benedicte, Deblaere, Karel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802836/
https://www.ncbi.nlm.nih.gov/pubmed/31634381
http://dx.doi.org/10.1371/journal.pone.0224130
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author De Meulenaere, Valerie
Bonte, Ellen
Verhoeven, Jeroen
Kalala Okito, Jean-Pierre
Pieters, Leen
Vral, Anne
De Wever, Olivier
Leybaert, Luc
Goethals, Ingeborg
Vanhove, Christian
Descamps, Benedicte
Deblaere, Karel
author_facet De Meulenaere, Valerie
Bonte, Ellen
Verhoeven, Jeroen
Kalala Okito, Jean-Pierre
Pieters, Leen
Vral, Anne
De Wever, Olivier
Leybaert, Luc
Goethals, Ingeborg
Vanhove, Christian
Descamps, Benedicte
Deblaere, Karel
author_sort De Meulenaere, Valerie
collection PubMed
description PURPOSE: Even with an optimal treatment protocol, the median survival of glioblastoma (GB) patients is only 12–15 months. Hence, there is need for novel effective therapies that improve survival outcomes. Recent evidence suggests an important role for connexin (Cx) proteins (especially Cx43) in the microenvironment of malignant glioma. Cx43-mediated gap junctional communication has been observed between tumor cells, between astrocytes and between tumor cells and astrocytes. Therefore, gap junction directed therapy using a pharmacological suppressor or modulator, such as tonabersat, could be a promising target in the treatment of GB. In this preclinical study, we evaluated the possible therapeutic potential of tonabersat in the F98 model. PROCEDURES: Female Fischer rats were inoculated with ± 25.000 F98 tumor cells in the right frontal lobe. Eight days post-inoculation contrast-enhanced T1-weighted (CE-T1w) magnetic resonance (MR) images were acquired to confirm tumor growth in the brain. After tumor confirmation, rats were randomized into a Control Group, a Connexin Modulation Group (CM), a Standard Medical Treatment Group (ST), and a Standard Medical Treatment with adjuvant Connexin Modulation Group (STCM). To evaluate therapy response, T2-weighted (T2w) and CE-T1w sequences were acquired at several time points. Tumor volume analysis was performed on CE-T1w images and statistical analysis was performed using a linear mixed model. RESULTS: Significant differences in estimated geometric mean tumor volumes were found between the ST Group and the Control Group and also between the STCM Group and the Control Group. In addition, significant differences in estimated geometric mean tumor volumes between the ST Group and the STCM Group were demonstrated. No significant differences in estimated geometric mean tumor volumes were found between the Control Group and the CM Group. CONCLUSION: Our results demonstrate a therapeutic potential of tonabersat for the treatment of GB when used in combination with radiotherapy and temozolomide chemotherapy.
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spelling pubmed-68028362019-11-02 Adjuvant therapeutic potential of tonabersat in the standard treatment of glioblastoma: A preclinical F98 glioblastoma rat model study De Meulenaere, Valerie Bonte, Ellen Verhoeven, Jeroen Kalala Okito, Jean-Pierre Pieters, Leen Vral, Anne De Wever, Olivier Leybaert, Luc Goethals, Ingeborg Vanhove, Christian Descamps, Benedicte Deblaere, Karel PLoS One Research Article PURPOSE: Even with an optimal treatment protocol, the median survival of glioblastoma (GB) patients is only 12–15 months. Hence, there is need for novel effective therapies that improve survival outcomes. Recent evidence suggests an important role for connexin (Cx) proteins (especially Cx43) in the microenvironment of malignant glioma. Cx43-mediated gap junctional communication has been observed between tumor cells, between astrocytes and between tumor cells and astrocytes. Therefore, gap junction directed therapy using a pharmacological suppressor or modulator, such as tonabersat, could be a promising target in the treatment of GB. In this preclinical study, we evaluated the possible therapeutic potential of tonabersat in the F98 model. PROCEDURES: Female Fischer rats were inoculated with ± 25.000 F98 tumor cells in the right frontal lobe. Eight days post-inoculation contrast-enhanced T1-weighted (CE-T1w) magnetic resonance (MR) images were acquired to confirm tumor growth in the brain. After tumor confirmation, rats were randomized into a Control Group, a Connexin Modulation Group (CM), a Standard Medical Treatment Group (ST), and a Standard Medical Treatment with adjuvant Connexin Modulation Group (STCM). To evaluate therapy response, T2-weighted (T2w) and CE-T1w sequences were acquired at several time points. Tumor volume analysis was performed on CE-T1w images and statistical analysis was performed using a linear mixed model. RESULTS: Significant differences in estimated geometric mean tumor volumes were found between the ST Group and the Control Group and also between the STCM Group and the Control Group. In addition, significant differences in estimated geometric mean tumor volumes between the ST Group and the STCM Group were demonstrated. No significant differences in estimated geometric mean tumor volumes were found between the Control Group and the CM Group. CONCLUSION: Our results demonstrate a therapeutic potential of tonabersat for the treatment of GB when used in combination with radiotherapy and temozolomide chemotherapy. Public Library of Science 2019-10-21 /pmc/articles/PMC6802836/ /pubmed/31634381 http://dx.doi.org/10.1371/journal.pone.0224130 Text en © 2019 De Meulenaere et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
De Meulenaere, Valerie
Bonte, Ellen
Verhoeven, Jeroen
Kalala Okito, Jean-Pierre
Pieters, Leen
Vral, Anne
De Wever, Olivier
Leybaert, Luc
Goethals, Ingeborg
Vanhove, Christian
Descamps, Benedicte
Deblaere, Karel
Adjuvant therapeutic potential of tonabersat in the standard treatment of glioblastoma: A preclinical F98 glioblastoma rat model study
title Adjuvant therapeutic potential of tonabersat in the standard treatment of glioblastoma: A preclinical F98 glioblastoma rat model study
title_full Adjuvant therapeutic potential of tonabersat in the standard treatment of glioblastoma: A preclinical F98 glioblastoma rat model study
title_fullStr Adjuvant therapeutic potential of tonabersat in the standard treatment of glioblastoma: A preclinical F98 glioblastoma rat model study
title_full_unstemmed Adjuvant therapeutic potential of tonabersat in the standard treatment of glioblastoma: A preclinical F98 glioblastoma rat model study
title_short Adjuvant therapeutic potential of tonabersat in the standard treatment of glioblastoma: A preclinical F98 glioblastoma rat model study
title_sort adjuvant therapeutic potential of tonabersat in the standard treatment of glioblastoma: a preclinical f98 glioblastoma rat model study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802836/
https://www.ncbi.nlm.nih.gov/pubmed/31634381
http://dx.doi.org/10.1371/journal.pone.0224130
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