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Drug Repositioning Screen on a New Primary Cell Line Identifies Potent Therapeutics for Glioblastoma

Glioblastoma is a malignant brain cancer with limited treatment options and high mortality rate. While established glioblastoma cell line models provide valuable information, they ultimately lose most primary characteristics of tumors under long-term serum culture conditions. Therefore, established...

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Autores principales: Senbabaoglu, Filiz, Aksu, Ali Cenk, Cingoz, Ahmet, Seker-Polat, Fidan, Borklu-Yucel, Esra, Solaroglu, İhsan, Bagci-Onder, Tugba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773901/
https://www.ncbi.nlm.nih.gov/pubmed/33390879
http://dx.doi.org/10.3389/fnins.2020.578316
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author Senbabaoglu, Filiz
Aksu, Ali Cenk
Cingoz, Ahmet
Seker-Polat, Fidan
Borklu-Yucel, Esra
Solaroglu, İhsan
Bagci-Onder, Tugba
author_facet Senbabaoglu, Filiz
Aksu, Ali Cenk
Cingoz, Ahmet
Seker-Polat, Fidan
Borklu-Yucel, Esra
Solaroglu, İhsan
Bagci-Onder, Tugba
author_sort Senbabaoglu, Filiz
collection PubMed
description Glioblastoma is a malignant brain cancer with limited treatment options and high mortality rate. While established glioblastoma cell line models provide valuable information, they ultimately lose most primary characteristics of tumors under long-term serum culture conditions. Therefore, established cell lines do not necessarily recapitulate genetic and morphological characteristics of real tumors. In this study, in line with the growing interest in using primary cell line models derived from patient tissue, we generated a primary glioblastoma cell line, KUGBM8 and characterized its genetic alterations, long term growth ability, tumor formation capacity and its response to Temozolomide, the front-line chemotherapy utilized clinically. In addition, we performed a drug repurposing screen on the KUGBM8 cell line to identify FDA-approved agents that can be incorporated into glioblastoma treatment regimen and identified Topotecan as a lead drug among 1,200 drugs. We showed Topotecan can induce cell death in KUGBM8 and other primary cell lines and cooperate with Temozolomide in low dosage combinations. Together, our study provides a new primary cell line model that can be suitable for both in vitro and in vivo studies and suggests that Topotecan can offer promise as a therapeutic approach for glioblastoma.
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spelling pubmed-77739012021-01-01 Drug Repositioning Screen on a New Primary Cell Line Identifies Potent Therapeutics for Glioblastoma Senbabaoglu, Filiz Aksu, Ali Cenk Cingoz, Ahmet Seker-Polat, Fidan Borklu-Yucel, Esra Solaroglu, İhsan Bagci-Onder, Tugba Front Neurosci Neuroscience Glioblastoma is a malignant brain cancer with limited treatment options and high mortality rate. While established glioblastoma cell line models provide valuable information, they ultimately lose most primary characteristics of tumors under long-term serum culture conditions. Therefore, established cell lines do not necessarily recapitulate genetic and morphological characteristics of real tumors. In this study, in line with the growing interest in using primary cell line models derived from patient tissue, we generated a primary glioblastoma cell line, KUGBM8 and characterized its genetic alterations, long term growth ability, tumor formation capacity and its response to Temozolomide, the front-line chemotherapy utilized clinically. In addition, we performed a drug repurposing screen on the KUGBM8 cell line to identify FDA-approved agents that can be incorporated into glioblastoma treatment regimen and identified Topotecan as a lead drug among 1,200 drugs. We showed Topotecan can induce cell death in KUGBM8 and other primary cell lines and cooperate with Temozolomide in low dosage combinations. Together, our study provides a new primary cell line model that can be suitable for both in vitro and in vivo studies and suggests that Topotecan can offer promise as a therapeutic approach for glioblastoma. Frontiers Media S.A. 2020-12-17 /pmc/articles/PMC7773901/ /pubmed/33390879 http://dx.doi.org/10.3389/fnins.2020.578316 Text en Copyright © 2020 Senbabaoglu, Aksu, Cingoz, Seker-Polat, Borklu-Yucel, Solaroglu and Bagci-Onder. http://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 Neuroscience
Senbabaoglu, Filiz
Aksu, Ali Cenk
Cingoz, Ahmet
Seker-Polat, Fidan
Borklu-Yucel, Esra
Solaroglu, İhsan
Bagci-Onder, Tugba
Drug Repositioning Screen on a New Primary Cell Line Identifies Potent Therapeutics for Glioblastoma
title Drug Repositioning Screen on a New Primary Cell Line Identifies Potent Therapeutics for Glioblastoma
title_full Drug Repositioning Screen on a New Primary Cell Line Identifies Potent Therapeutics for Glioblastoma
title_fullStr Drug Repositioning Screen on a New Primary Cell Line Identifies Potent Therapeutics for Glioblastoma
title_full_unstemmed Drug Repositioning Screen on a New Primary Cell Line Identifies Potent Therapeutics for Glioblastoma
title_short Drug Repositioning Screen on a New Primary Cell Line Identifies Potent Therapeutics for Glioblastoma
title_sort drug repositioning screen on a new primary cell line identifies potent therapeutics for glioblastoma
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773901/
https://www.ncbi.nlm.nih.gov/pubmed/33390879
http://dx.doi.org/10.3389/fnins.2020.578316
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