γH2AX foci assay in glioblastoma: Surgical specimen versus corresponding stem cell culture.


Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
06 2021
Historique:
received: 29 07 2020
revised: 02 12 2020
accepted: 17 03 2021
pubmed: 30 3 2021
medline: 29 6 2021
entrez: 29 3 2021
Statut: ppublish

Résumé

To assess radiation response using γH2AX assay in surgical specimens from glioblastoma (GB) patients and their corresponding primary gliosphere culture. To test the hypothesis that gliospheres (stem cell enriched) are more resistant than specimens (bulky cell dominated) but that the interpatient heterogeneity is similar. Ten pairs of specimens and corresponding gliospheres derived from patients with IDH-wildtype GB were studied. Specimens and gliospheres were irradiated with graded doses and after 24 h the number of residual γH2AX foci was counted. Gliospheres showed a higher Nestin expression than specimens and exhibited two different phenotypes: free floating (n = 7) and attached (n = 3). Slope analysis revealed an interpatient heterogeneity with values between 0.15 and 1.30 residual γH2AX foci/Gy. Free-floating spheres were more resistant than their parental specimens (median slope 0.13 foci/Gy versus 0.53) as well as than the attached spheres (2.14). The slopes of free floating spheres did not correlate with their corresponding specimens while a trend for a positive correlation was found for the attached spheres and the respective specimens. Association with MGMT did not reach statistical significance. Consistent with the clinical phenotype and our previous experiments, GB specimens show low radiation sensitivity. Stem-cell enriched free-floating gliospheres were more resistant than specimens supporting the concept of radioresistance in stem cell-like cells. The lack of correlation between specimens and their respective gliosphere cultures needs validation and may have a profound impact on future translational studies using γH2AX as a potential biomarker for personalized radiation therapy.

Identifiants

pubmed: 33775712
pii: S0167-8140(21)06160-0
doi: 10.1016/j.radonc.2021.03.023
pii:
doi:

Substances chimiques

Histones 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

119-125

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Andreas Riedel (A)

Radiation Oncology, Medical Faculty and University Hospital Tübingen, Germany.

Lukas Klumpp (L)

Radiation Oncology, Medical Faculty and University Hospital Tübingen, Germany.

Apostolos Menegakis (A)

Netherlands Cancer Institute, Division of Cell Biology, Amsterdam, The Netherlands.

Chiara De-Colle (C)

Radiation Oncology, Medical Faculty and University Hospital Tübingen, Germany.

Stephan M Huber (SM)

Radiation Oncology, Medical Faculty and University Hospital Tübingen, Germany.

Jens Schittenhelm (J)

Division of Neuropathology, Medical Faculty and University Hospital Tübingen, Germany.

Manuela Neumann (M)

Division of Neuropathology, Medical Faculty and University Hospital Tübingen, Germany.

Susan Noell (S)

Department of Neurosurgery, Medical Faculty and University Hospital Tübingen, Germany.

Marcos Tatagiba (M)

Department of Neurosurgery, Medical Faculty and University Hospital Tübingen, Germany.

Daniel Zips (D)

Radiation Oncology, Medical Faculty and University Hospital Tübingen, Germany; German Cancer Consortium (DKTK), Partner Site Tübingen, Germany; German Cancer Research Center (DKFZ), Heidelberg, Germany. Electronic address: daniel.zips@med.uni-tuebingen.de.

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