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Effect of axitinib regulating the pathological blood–brain barrier functional recovery for glioblastoma therapeutics
AIMS: Dysfunction of the blood–brain barrier (BBB) is a prominent pathological feature of glioblastoma (GBM). Vascular endothelial growth factor (VEGF) is confirmed to be abnormally elevated in the pathogenesis of GBM, causing BBB pathological disruption, which further allows the leakage of neurotox...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841308/ https://www.ncbi.nlm.nih.gov/pubmed/34967104 http://dx.doi.org/10.1111/cns.13788 |
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author | Zhang, Fengtian Wen, Lijuan Wang, Kai Huang, Zhihua Jin, Xiangyu Xiong, Ruiwen He, Shiying Hu, Fuqiang |
author_facet | Zhang, Fengtian Wen, Lijuan Wang, Kai Huang, Zhihua Jin, Xiangyu Xiong, Ruiwen He, Shiying Hu, Fuqiang |
author_sort | Zhang, Fengtian |
collection | PubMed |
description | AIMS: Dysfunction of the blood–brain barrier (BBB) is a prominent pathological feature of glioblastoma (GBM). Vascular endothelial growth factor (VEGF) is confirmed to be abnormally elevated in the pathogenesis of GBM, causing BBB pathological disruption, which further allows the leakage of neurotoxic blood‐derived molecules into the central nervous system (CNS), interfering brain homeostasis and leading to poor patient outcome. Since BBB is an integral and pivotal part of the brain microenvironment, which strongly supports the occurrence and the pathological progression of GBM, here we have selected the VEGFR antagonist axitinib as a BBB functional regulator and hypothesized to regulate pathological BBB restoration for GBM effective treatment. METHODS: The pathological BBB cell model was constructed to investigate the timeliness and dose effect of axitinib regulating pathological BBB restoration. In order to investigate the efficacy and safety of axitinib regulating pathological BBB restoration for anti‐GBM treatment, the orthotropic GBM‐bearing mice model was established for in vivo study, and bioluminescent imaging was used to real‐time and noninvasively monitor tumor growth response in vivo, and survival time was also recorded. RESULTS: Axitinib under non‐cytotoxic dosage regulated pathological BBB restoration in a time‐dependent mode, and multiple intervention of axitinib could realize a visible restoration of pathological BBB in vitro. Moreover, axitinib treatment restored pathological BBB in orthotropic GBM‐bearing mice. We further confirmed that functional restoration of pathological BBB with axitinib had certain curative effect in prolonging median survival of orthotropic GBM‐bearing mice at non‐cytotoxic dosages in vivo. CONCLUSION: The mechanism of axitinib involved in BBB functional regulation in the treatment of GBM is first illuminated in this report; moreover, this is the first report first referring to regulating pathological BBB functional recovery for GBM effective therapeutics. Overall, the view of regulating pathological BBB functional recovery may offer a novel sight for other CNS diseases relating to BBB permeability effective therapeutics. |
format | Online Article Text |
id | pubmed-8841308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88413082022-02-22 Effect of axitinib regulating the pathological blood–brain barrier functional recovery for glioblastoma therapeutics Zhang, Fengtian Wen, Lijuan Wang, Kai Huang, Zhihua Jin, Xiangyu Xiong, Ruiwen He, Shiying Hu, Fuqiang CNS Neurosci Ther Original Articles AIMS: Dysfunction of the blood–brain barrier (BBB) is a prominent pathological feature of glioblastoma (GBM). Vascular endothelial growth factor (VEGF) is confirmed to be abnormally elevated in the pathogenesis of GBM, causing BBB pathological disruption, which further allows the leakage of neurotoxic blood‐derived molecules into the central nervous system (CNS), interfering brain homeostasis and leading to poor patient outcome. Since BBB is an integral and pivotal part of the brain microenvironment, which strongly supports the occurrence and the pathological progression of GBM, here we have selected the VEGFR antagonist axitinib as a BBB functional regulator and hypothesized to regulate pathological BBB restoration for GBM effective treatment. METHODS: The pathological BBB cell model was constructed to investigate the timeliness and dose effect of axitinib regulating pathological BBB restoration. In order to investigate the efficacy and safety of axitinib regulating pathological BBB restoration for anti‐GBM treatment, the orthotropic GBM‐bearing mice model was established for in vivo study, and bioluminescent imaging was used to real‐time and noninvasively monitor tumor growth response in vivo, and survival time was also recorded. RESULTS: Axitinib under non‐cytotoxic dosage regulated pathological BBB restoration in a time‐dependent mode, and multiple intervention of axitinib could realize a visible restoration of pathological BBB in vitro. Moreover, axitinib treatment restored pathological BBB in orthotropic GBM‐bearing mice. We further confirmed that functional restoration of pathological BBB with axitinib had certain curative effect in prolonging median survival of orthotropic GBM‐bearing mice at non‐cytotoxic dosages in vivo. CONCLUSION: The mechanism of axitinib involved in BBB functional regulation in the treatment of GBM is first illuminated in this report; moreover, this is the first report first referring to regulating pathological BBB functional recovery for GBM effective therapeutics. Overall, the view of regulating pathological BBB functional recovery may offer a novel sight for other CNS diseases relating to BBB permeability effective therapeutics. John Wiley and Sons Inc. 2021-12-29 /pmc/articles/PMC8841308/ /pubmed/34967104 http://dx.doi.org/10.1111/cns.13788 Text en © 2021 The Authors. CNS Neuroscience & Therapeutics Published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Zhang, Fengtian Wen, Lijuan Wang, Kai Huang, Zhihua Jin, Xiangyu Xiong, Ruiwen He, Shiying Hu, Fuqiang Effect of axitinib regulating the pathological blood–brain barrier functional recovery for glioblastoma therapeutics |
title | Effect of axitinib regulating the pathological blood–brain barrier functional recovery for glioblastoma therapeutics |
title_full | Effect of axitinib regulating the pathological blood–brain barrier functional recovery for glioblastoma therapeutics |
title_fullStr | Effect of axitinib regulating the pathological blood–brain barrier functional recovery for glioblastoma therapeutics |
title_full_unstemmed | Effect of axitinib regulating the pathological blood–brain barrier functional recovery for glioblastoma therapeutics |
title_short | Effect of axitinib regulating the pathological blood–brain barrier functional recovery for glioblastoma therapeutics |
title_sort | effect of axitinib regulating the pathological blood–brain barrier functional recovery for glioblastoma therapeutics |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841308/ https://www.ncbi.nlm.nih.gov/pubmed/34967104 http://dx.doi.org/10.1111/cns.13788 |
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