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Isolation of Circulating Tumour Cells in Patients With Glioblastoma Using Spiral Microfluidic Technology – A Pilot Study

Glioblastoma (GBM) is the most common and aggressive type of tumour arising from the central nervous system. GBM remains an incurable disease despite advancement in therapies, with overall survival of approximately 15 months. Recent literature has highlighted that GBM releases tumoural content which...

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Autores principales: Müller Bark, Juliana, Kulasinghe, Arutha, Hartel, Gunter, Leo, Paul, Warkiani, Majid Ebrahimi, Jeffree, Rosalind L., Chua, Benjamin, Day, Bryan W., Punyadeera, Chamindie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210776/
https://www.ncbi.nlm.nih.gov/pubmed/34150645
http://dx.doi.org/10.3389/fonc.2021.681130
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author Müller Bark, Juliana
Kulasinghe, Arutha
Hartel, Gunter
Leo, Paul
Warkiani, Majid Ebrahimi
Jeffree, Rosalind L.
Chua, Benjamin
Day, Bryan W.
Punyadeera, Chamindie
author_facet Müller Bark, Juliana
Kulasinghe, Arutha
Hartel, Gunter
Leo, Paul
Warkiani, Majid Ebrahimi
Jeffree, Rosalind L.
Chua, Benjamin
Day, Bryan W.
Punyadeera, Chamindie
author_sort Müller Bark, Juliana
collection PubMed
description Glioblastoma (GBM) is the most common and aggressive type of tumour arising from the central nervous system. GBM remains an incurable disease despite advancement in therapies, with overall survival of approximately 15 months. Recent literature has highlighted that GBM releases tumoural content which crosses the blood-brain barrier (BBB) and is detected in patients’ blood, such as circulating tumour cells (CTCs). CTCs carry tumour information and have shown promise as prognostic and predictive biomarkers in different cancer types. Currently, there is limited data for the clinical utility of CTCs in GBM. Here, we report the use of spiral microfluidic technology to isolate CTCs from whole blood of newly diagnosed GBM patients before and after surgery, followed by characterization for GFAP, cell-surface vimentin protein expression and EGFR amplification. CTCs were found in 13 out of 20 patients (9/20 before surgery and 11/19 after surgery). Patients with CTC counts equal to 0 after surgery had a significantly longer recurrence-free survival (p=0.0370). This is the first investigation using the spiral microfluidics technology for the enrichment of CTCs from GBM patients and these results support the use of this technology to better understand the clinical value of CTCs in the management of GBM in future studies.
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spelling pubmed-82107762021-06-18 Isolation of Circulating Tumour Cells in Patients With Glioblastoma Using Spiral Microfluidic Technology – A Pilot Study Müller Bark, Juliana Kulasinghe, Arutha Hartel, Gunter Leo, Paul Warkiani, Majid Ebrahimi Jeffree, Rosalind L. Chua, Benjamin Day, Bryan W. Punyadeera, Chamindie Front Oncol Oncology Glioblastoma (GBM) is the most common and aggressive type of tumour arising from the central nervous system. GBM remains an incurable disease despite advancement in therapies, with overall survival of approximately 15 months. Recent literature has highlighted that GBM releases tumoural content which crosses the blood-brain barrier (BBB) and is detected in patients’ blood, such as circulating tumour cells (CTCs). CTCs carry tumour information and have shown promise as prognostic and predictive biomarkers in different cancer types. Currently, there is limited data for the clinical utility of CTCs in GBM. Here, we report the use of spiral microfluidic technology to isolate CTCs from whole blood of newly diagnosed GBM patients before and after surgery, followed by characterization for GFAP, cell-surface vimentin protein expression and EGFR amplification. CTCs were found in 13 out of 20 patients (9/20 before surgery and 11/19 after surgery). Patients with CTC counts equal to 0 after surgery had a significantly longer recurrence-free survival (p=0.0370). This is the first investigation using the spiral microfluidics technology for the enrichment of CTCs from GBM patients and these results support the use of this technology to better understand the clinical value of CTCs in the management of GBM in future studies. Frontiers Media S.A. 2021-06-03 /pmc/articles/PMC8210776/ /pubmed/34150645 http://dx.doi.org/10.3389/fonc.2021.681130 Text en Copyright © 2021 Müller Bark, Kulasinghe, Hartel, Leo, Warkiani, Jeffree, Chua, Day and Punyadeera 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 Oncology
Müller Bark, Juliana
Kulasinghe, Arutha
Hartel, Gunter
Leo, Paul
Warkiani, Majid Ebrahimi
Jeffree, Rosalind L.
Chua, Benjamin
Day, Bryan W.
Punyadeera, Chamindie
Isolation of Circulating Tumour Cells in Patients With Glioblastoma Using Spiral Microfluidic Technology – A Pilot Study
title Isolation of Circulating Tumour Cells in Patients With Glioblastoma Using Spiral Microfluidic Technology – A Pilot Study
title_full Isolation of Circulating Tumour Cells in Patients With Glioblastoma Using Spiral Microfluidic Technology – A Pilot Study
title_fullStr Isolation of Circulating Tumour Cells in Patients With Glioblastoma Using Spiral Microfluidic Technology – A Pilot Study
title_full_unstemmed Isolation of Circulating Tumour Cells in Patients With Glioblastoma Using Spiral Microfluidic Technology – A Pilot Study
title_short Isolation of Circulating Tumour Cells in Patients With Glioblastoma Using Spiral Microfluidic Technology – A Pilot Study
title_sort isolation of circulating tumour cells in patients with glioblastoma using spiral microfluidic technology – a pilot study
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210776/
https://www.ncbi.nlm.nih.gov/pubmed/34150645
http://dx.doi.org/10.3389/fonc.2021.681130
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