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Tumor Treating Fields (TTFields) Reversibly Permeabilize the Blood–Brain Barrier In Vitro and In Vivo
Despite the availability of numerous therapeutic substances that could potentially target CNS disorders, an inability of these agents to cross the restrictive blood–brain barrier (BBB) limits their clinical utility. Novel strategies to overcome the BBB are therefore needed to improve drug delivery....
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599321/ https://www.ncbi.nlm.nih.gov/pubmed/36291557 http://dx.doi.org/10.3390/biom12101348 |
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author | Salvador, Ellaine Kessler, Almuth F. Domröse, Dominik Hörmann, Julia Schaeffer, Clara Giniunaite, Aiste Burek, Malgorzata Tempel-Brami, Catherine Voloshin, Tali Volodin, Alexandra Zeidan, Adel Giladi, Moshe Ernestus, Ralf-Ingo Löhr, Mario Förster, Carola Y. Hagemann, Carsten |
author_facet | Salvador, Ellaine Kessler, Almuth F. Domröse, Dominik Hörmann, Julia Schaeffer, Clara Giniunaite, Aiste Burek, Malgorzata Tempel-Brami, Catherine Voloshin, Tali Volodin, Alexandra Zeidan, Adel Giladi, Moshe Ernestus, Ralf-Ingo Löhr, Mario Förster, Carola Y. Hagemann, Carsten |
author_sort | Salvador, Ellaine |
collection | PubMed |
description | Despite the availability of numerous therapeutic substances that could potentially target CNS disorders, an inability of these agents to cross the restrictive blood–brain barrier (BBB) limits their clinical utility. Novel strategies to overcome the BBB are therefore needed to improve drug delivery. We report, for the first time, how Tumor Treating Fields (TTFields), approved for glioblastoma (GBM), affect the BBB’s integrity and permeability. Here, we treated murine microvascular cerebellar endothelial cells (cerebEND) with 100–300 kHz TTFields for up to 72 h and analyzed the expression of barrier proteins by immunofluorescence staining and Western blot. In vivo, compounds normally unable to cross the BBB were traced in healthy rat brain following TTFields administration at 100 kHz. The effects were analyzed via MRI and immunohistochemical staining of tight-junction proteins. Furthermore, GBM tumor-bearing rats were treated with paclitaxel (PTX), a chemotherapeutic normally restricted by the BBB combined with TTFields at 100 kHz. The tumor volume was reduced with TTFields plus PTX, relative to either treatment alone. In vitro, we demonstrate that TTFields transiently disrupted BBB function at 100 kHz through a Rho kinase-mediated tight junction claudin-5 phosphorylation pathway. Altogether, if translated into clinical use, TTFields could represent a novel CNS drug delivery strategy. |
format | Online Article Text |
id | pubmed-9599321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95993212022-10-27 Tumor Treating Fields (TTFields) Reversibly Permeabilize the Blood–Brain Barrier In Vitro and In Vivo Salvador, Ellaine Kessler, Almuth F. Domröse, Dominik Hörmann, Julia Schaeffer, Clara Giniunaite, Aiste Burek, Malgorzata Tempel-Brami, Catherine Voloshin, Tali Volodin, Alexandra Zeidan, Adel Giladi, Moshe Ernestus, Ralf-Ingo Löhr, Mario Förster, Carola Y. Hagemann, Carsten Biomolecules Article Despite the availability of numerous therapeutic substances that could potentially target CNS disorders, an inability of these agents to cross the restrictive blood–brain barrier (BBB) limits their clinical utility. Novel strategies to overcome the BBB are therefore needed to improve drug delivery. We report, for the first time, how Tumor Treating Fields (TTFields), approved for glioblastoma (GBM), affect the BBB’s integrity and permeability. Here, we treated murine microvascular cerebellar endothelial cells (cerebEND) with 100–300 kHz TTFields for up to 72 h and analyzed the expression of barrier proteins by immunofluorescence staining and Western blot. In vivo, compounds normally unable to cross the BBB were traced in healthy rat brain following TTFields administration at 100 kHz. The effects were analyzed via MRI and immunohistochemical staining of tight-junction proteins. Furthermore, GBM tumor-bearing rats were treated with paclitaxel (PTX), a chemotherapeutic normally restricted by the BBB combined with TTFields at 100 kHz. The tumor volume was reduced with TTFields plus PTX, relative to either treatment alone. In vitro, we demonstrate that TTFields transiently disrupted BBB function at 100 kHz through a Rho kinase-mediated tight junction claudin-5 phosphorylation pathway. Altogether, if translated into clinical use, TTFields could represent a novel CNS drug delivery strategy. MDPI 2022-09-22 /pmc/articles/PMC9599321/ /pubmed/36291557 http://dx.doi.org/10.3390/biom12101348 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Salvador, Ellaine Kessler, Almuth F. Domröse, Dominik Hörmann, Julia Schaeffer, Clara Giniunaite, Aiste Burek, Malgorzata Tempel-Brami, Catherine Voloshin, Tali Volodin, Alexandra Zeidan, Adel Giladi, Moshe Ernestus, Ralf-Ingo Löhr, Mario Förster, Carola Y. Hagemann, Carsten Tumor Treating Fields (TTFields) Reversibly Permeabilize the Blood–Brain Barrier In Vitro and In Vivo |
title | Tumor Treating Fields (TTFields) Reversibly Permeabilize the Blood–Brain Barrier In Vitro and In Vivo |
title_full | Tumor Treating Fields (TTFields) Reversibly Permeabilize the Blood–Brain Barrier In Vitro and In Vivo |
title_fullStr | Tumor Treating Fields (TTFields) Reversibly Permeabilize the Blood–Brain Barrier In Vitro and In Vivo |
title_full_unstemmed | Tumor Treating Fields (TTFields) Reversibly Permeabilize the Blood–Brain Barrier In Vitro and In Vivo |
title_short | Tumor Treating Fields (TTFields) Reversibly Permeabilize the Blood–Brain Barrier In Vitro and In Vivo |
title_sort | tumor treating fields (ttfields) reversibly permeabilize the blood–brain barrier in vitro and in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599321/ https://www.ncbi.nlm.nih.gov/pubmed/36291557 http://dx.doi.org/10.3390/biom12101348 |
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