Abrogation of radioresistance in glioblastoma stem-like cells by inhibition of ATM kinase
Carruthers, Ross and Ahmed, Shafiq U. and Strathdee, Karen and Gomez-Roman, Natividad and Amoah-Buahin, Evelyn and Watts, Colin and Chalmers, Anthony J. (2015) Abrogation of radioresistance in glioblastoma stem-like cells by inhibition of ATM kinase. Molecular Oncology, 9 (1). pp. 192-203. ISSN 1878-0261 (https://doi.org/10.1016/j.molonc.2014.08.003)
Preview |
Text.
Filename: Carruthers_etal_MO2015_Abrogation_radioresistance_glioblastoma_stem_like_cells_inhibition_ATM_kinase.pdf
Final Published Version License: Download (1MB)| Preview |
Abstract
Resistance to radiotherapy in glioblastoma (GBM) is an important clinical problem and several authors have attributed this to a subpopulation of GBM cancer stem cells (CSCs) which may be responsible for tumour recurrence following treatment. It is hypothesised that GBM CSCs exhibit upregulated DNA damage responses and are resistant to radiation but the current literature is conflicting. We investigated radioresistance of primary GBM cells grown in stem cell conditions (CSC) compared to paired differentiated tumour cell populations and explored the radiosensitising effects of the ATM inhibitor KU-55933.We report that GBM CSCs are radioresistant compared to paired differentiated tumour cells as measured by clonogenic assay. GBM CSC's display upregulated phosphorylated DNA damage response proteins and enhanced activation of the G2/M checkpoint following irradiation and repair DNA double strand breaks (DSBs) more efficiently than their differentiated tumour cell counterparts following radiation.Inhibition of ATM kinase by KU-55933 produced potent radiosensitisation of GBM CSCs (sensitiser enhancement ratios 2.6-3.5) and effectively abrogated the enhanced DSB repair proficiency observed in GBM CSCs at 24h post irradiation. G2/M checkpoint activation was reduced but not abolished by KU-55933 in GBM CSCs.ATM kinase inhibition overcomes radioresistance of GBM CSCs and, in combination with conventional therapy, has potential to improve outcomes for patients with GBM.
ORCID iDs
Carruthers, Ross, Ahmed, Shafiq U., Strathdee, Karen, Gomez-Roman, Natividad ORCID: https://orcid.org/0000-0002-2325-7517, Amoah-Buahin, Evelyn, Watts, Colin and Chalmers, Anthony J.;-
-
Item type: Article ID code: 74855 Dates: DateEvent1 January 2015Published15 August 2014AcceptedSubjects: Medicine Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 10 Dec 2020 09:45 Last modified: 11 Nov 2024 12:55 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/74855