Preparation and characterization of size-controlled glioma spheroids using agarose hydrogel microwells.

Treatment of glioblastoma, the most common and aggressive type of primary brain tumors, is a major medical challenge and the development of new alternatives requires simple yet realistic models for these tumors. In vitro spheroid models offer attractive platforms to mimic the tumor behavior in vivo...

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Main Authors: Fereshtehsadat Mirab, You Jung Kang, Sheereen Majd
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0211078
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spelling doaj-8f078117bc9c439991b005ec3c7324c82021-03-03T20:56:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01141e021107810.1371/journal.pone.0211078Preparation and characterization of size-controlled glioma spheroids using agarose hydrogel microwells.Fereshtehsadat MirabYou Jung KangSheereen MajdTreatment of glioblastoma, the most common and aggressive type of primary brain tumors, is a major medical challenge and the development of new alternatives requires simple yet realistic models for these tumors. In vitro spheroid models offer attractive platforms to mimic the tumor behavior in vivo and have thus, been increasingly applied for assessment of drug efficacy in various tumors. The aim of this study was to produce and characterize size-controlled U251 glioma spheroids towards application in glioma drug evaluation studies. To this end, we fabricated agarose hydrogel microwells with cylindrical shape and diameters of 70-700 μm and applied these wells without any surface modification for glioma spheroid formation. The resultant spheroids were homogeneous in size and shape, exhibited high cell viability (> 90%), and had a similar growth rate to that of natural brain tumors. The final size of spheroids depended on cell seeding density and microwell size. The spheroids' volume increased linearly with the cell seeding density and the rate of this change increased with the well size. Lastly, we tested the therapeutic effect of an anti-cancer drug, Di-2-pyridylketone-4,4-dimethyl-3-thiosemicarbazone (Dp44mT) on the resultant glioma spheroids and demonstrated the applicability of this spheroid model for drug efficacy studies.https://doi.org/10.1371/journal.pone.0211078
collection DOAJ
language English
format Article
sources DOAJ
author Fereshtehsadat Mirab
You Jung Kang
Sheereen Majd
spellingShingle Fereshtehsadat Mirab
You Jung Kang
Sheereen Majd
Preparation and characterization of size-controlled glioma spheroids using agarose hydrogel microwells.
PLoS ONE
author_facet Fereshtehsadat Mirab
You Jung Kang
Sheereen Majd
author_sort Fereshtehsadat Mirab
title Preparation and characterization of size-controlled glioma spheroids using agarose hydrogel microwells.
title_short Preparation and characterization of size-controlled glioma spheroids using agarose hydrogel microwells.
title_full Preparation and characterization of size-controlled glioma spheroids using agarose hydrogel microwells.
title_fullStr Preparation and characterization of size-controlled glioma spheroids using agarose hydrogel microwells.
title_full_unstemmed Preparation and characterization of size-controlled glioma spheroids using agarose hydrogel microwells.
title_sort preparation and characterization of size-controlled glioma spheroids using agarose hydrogel microwells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description Treatment of glioblastoma, the most common and aggressive type of primary brain tumors, is a major medical challenge and the development of new alternatives requires simple yet realistic models for these tumors. In vitro spheroid models offer attractive platforms to mimic the tumor behavior in vivo and have thus, been increasingly applied for assessment of drug efficacy in various tumors. The aim of this study was to produce and characterize size-controlled U251 glioma spheroids towards application in glioma drug evaluation studies. To this end, we fabricated agarose hydrogel microwells with cylindrical shape and diameters of 70-700 μm and applied these wells without any surface modification for glioma spheroid formation. The resultant spheroids were homogeneous in size and shape, exhibited high cell viability (> 90%), and had a similar growth rate to that of natural brain tumors. The final size of spheroids depended on cell seeding density and microwell size. The spheroids' volume increased linearly with the cell seeding density and the rate of this change increased with the well size. Lastly, we tested the therapeutic effect of an anti-cancer drug, Di-2-pyridylketone-4,4-dimethyl-3-thiosemicarbazone (Dp44mT) on the resultant glioma spheroids and demonstrated the applicability of this spheroid model for drug efficacy studies.
url https://doi.org/10.1371/journal.pone.0211078
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