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3D models of glioblastoma interaction with cortical cells

Introduction: Glioblastoma (GBM) invasiveness and ability to infiltrate deep into the brain tissue is a major reason for the poor patient prognosis for this type of brain cancer. Behavior of glioblastoma cells, including their motility, and expression of invasion-promoting genes such as matrix metal...

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Autores principales: Abedin, Md Joynal, Michelhaugh, Sharon K., Mittal, Sandeep, Berdichevsky, Yevgeny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033518/
https://www.ncbi.nlm.nih.gov/pubmed/36970613
http://dx.doi.org/10.3389/fbioe.2023.1150772
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author Abedin, Md Joynal
Michelhaugh, Sharon K.
Mittal, Sandeep
Berdichevsky, Yevgeny
author_facet Abedin, Md Joynal
Michelhaugh, Sharon K.
Mittal, Sandeep
Berdichevsky, Yevgeny
author_sort Abedin, Md Joynal
collection PubMed
description Introduction: Glioblastoma (GBM) invasiveness and ability to infiltrate deep into the brain tissue is a major reason for the poor patient prognosis for this type of brain cancer. Behavior of glioblastoma cells, including their motility, and expression of invasion-promoting genes such as matrix metalloprotease-2 (MMP2), are strongly influenced by normal cells found in the brain parenchyma. Cells such as neurons may also be influenced by the tumor, as many glioblastoma patients develop epilepsy. In vitro models of glioblastoma invasiveness are used to supplement animal models in a search for better treatments, and need to combine capability for high-throughput experiments with capturing bidirectional interactions between GBM and brain cells. Methods: In this work, two 3D in vitro models of GBM-cortical interactions were investigated. A matrix-free model was created by co-culturing GBM and cortical spheroids, and a matrix-based model was created by embedding cortical cells and a GBM spheroid in Matrigel. Results: Rapid GBM invasion occurred in the matrix-based model, and was enhanced by the presence of cortical cells. Little invasion occurred in the matrix-free model. In both types of models, presence of GBM cells resulted in a significant increase in paroxysmal neuronal activity. Discussion: Matrix-based model may be better suited for studying GBM invasion in an environment that includes cortical cells, while matrix-free model may be useful in investigation of tumor-associated epilepsy.
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spelling pubmed-100335182023-03-24 3D models of glioblastoma interaction with cortical cells Abedin, Md Joynal Michelhaugh, Sharon K. Mittal, Sandeep Berdichevsky, Yevgeny Front Bioeng Biotechnol Bioengineering and Biotechnology Introduction: Glioblastoma (GBM) invasiveness and ability to infiltrate deep into the brain tissue is a major reason for the poor patient prognosis for this type of brain cancer. Behavior of glioblastoma cells, including their motility, and expression of invasion-promoting genes such as matrix metalloprotease-2 (MMP2), are strongly influenced by normal cells found in the brain parenchyma. Cells such as neurons may also be influenced by the tumor, as many glioblastoma patients develop epilepsy. In vitro models of glioblastoma invasiveness are used to supplement animal models in a search for better treatments, and need to combine capability for high-throughput experiments with capturing bidirectional interactions between GBM and brain cells. Methods: In this work, two 3D in vitro models of GBM-cortical interactions were investigated. A matrix-free model was created by co-culturing GBM and cortical spheroids, and a matrix-based model was created by embedding cortical cells and a GBM spheroid in Matrigel. Results: Rapid GBM invasion occurred in the matrix-based model, and was enhanced by the presence of cortical cells. Little invasion occurred in the matrix-free model. In both types of models, presence of GBM cells resulted in a significant increase in paroxysmal neuronal activity. Discussion: Matrix-based model may be better suited for studying GBM invasion in an environment that includes cortical cells, while matrix-free model may be useful in investigation of tumor-associated epilepsy. Frontiers Media S.A. 2023-03-09 /pmc/articles/PMC10033518/ /pubmed/36970613 http://dx.doi.org/10.3389/fbioe.2023.1150772 Text en Copyright © 2023 Abedin, Michelhaugh, Mittal and Berdichevsky. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Abedin, Md Joynal
Michelhaugh, Sharon K.
Mittal, Sandeep
Berdichevsky, Yevgeny
3D models of glioblastoma interaction with cortical cells
title 3D models of glioblastoma interaction with cortical cells
title_full 3D models of glioblastoma interaction with cortical cells
title_fullStr 3D models of glioblastoma interaction with cortical cells
title_full_unstemmed 3D models of glioblastoma interaction with cortical cells
title_short 3D models of glioblastoma interaction with cortical cells
title_sort 3d models of glioblastoma interaction with cortical cells
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033518/
https://www.ncbi.nlm.nih.gov/pubmed/36970613
http://dx.doi.org/10.3389/fbioe.2023.1150772
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