Evidence map›Paper›PMID 33478100›Full record

ArticleCancers2021

Identification of a Dexamethasone Mediated Radioprotection Mechanism Reveals New Therapeutic Vulnerabilities in Glioblastoma.

Paula Aldaz, Jaione Auzmendi-Iriarte, Maika Durántez, Irene Lasheras-Otero, Estefania Carrasco-Garcia, M Victoria Zelaya, Laura Bragado, Ana Olías-Arjona, Larraitz Egaña, Nicolás Samprón and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 6 institutions in 2 countries.

Paula AldazCancer Signalling Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), 31008 Pamplona, Spain.
Jaione Auzmendi-IriarteCellular Oncology Group, Biodonostia Health Research Institute, 20014 San Sebastian, Spain.
Maika DurántezCancer Signalling Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), 31008 Pamplona, Spain.
Irene Lasheras-OteroCancer Signalling Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), 31008 Pamplona, Spain.
Estefania Carrasco-GarciaCellular Oncology Group, Biodonostia Health Research Institute, 20014 San Sebastian, Spain.
M Victoria ZelayaHealth Research Institute of Navarre (IdiSNA), 31008 Pamplona, Spain.
Laura BragadoHealth Research Institute of Navarre (IdiSNA), 31008 Pamplona, Spain.
Ana Olías-ArjonaCancer Signalling Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), 31008 Pamplona, Spain.
Larraitz EgañaCellular Oncology Group, Biodonostia Health Research Institute, 20014 San Sebastian, Spain.
Nicolás SamprónCellular Oncology Group, Biodonostia Health Research Institute, 20014 San Sebastian, Spain.
Idoia MorillaCancer Signalling Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), 31008 Pamplona, Spain.
Marta Redondo-MuñozCancer Signalling Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), 31008 Pamplona, Spain.
Mikel RicoHealth Research Institute of Navarre (IdiSNA), 31008 Pamplona, Spain.
Massimo SquatritoSeve-Ballesteros Foundation Brain Tumor Group, Cancer Cell Biology Program, Spanish National Cancer Research Centre (CNIO), 28029 Madrid, Spain.
Marta Maria-AlonsoHealth Research Institute of Navarre (IdiSNA), 31008 Pamplona, Spain.ORCID 0000-0002-7520-7351
Joaquín Fernández-IrigoyenHealth Research Institute of Navarre (IdiSNA), 31008 Pamplona, Spain.
Enrique SantamariaHealth Research Institute of Navarre (IdiSNA), 31008 Pamplona, Spain.
Iñaki M LarráyozCenter for Biomedical Research of La Rioja (CIBIR), Neurodegeneration Area, Biomarkers and Molecular Signaling Group, 26006 Logroño, Spain.
Claudia WellbrockCancer Signalling Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), 31008 Pamplona, Spain.
Ander MatheuCellular Oncology Group, Biodonostia Health Research Institute, 20014 San Sebastian, Spain.
Imanol ArozarenaCancer Signalling Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), 31008 Pamplona, Spain.ORCID 0000-0001-6349-2442
Universidad Publica de Navarra · ESNavarre Institute of Health Research · ESBiogipuzkoa Health Research Institute · ESCenter for Biomedical Research of La Rioja · ESIkerbasque · ESSpanish National Cancer Research Centre · ES

Funding

Department of Education, University and Research of the Basque Government PRE_2016_1_0375Health Department of the Basque Country DTS18/00181Industry Department of the Government of Navarra PI1054Industry Department of the Government of Navarra PI1059Instituto de Salud Carlos III-FEDER PI15/00176Instituto de Salud Carlos III-FEDER PI16/0158Instituto de Salud Carlos III-FEDER PT17/0019/009Miguel Servet Carlos III CP15/00176
6 · The paper itself

Abstract

(1) Background: Despite the indisputable effectiveness of dexamethasone (DEXA) to reduce inflammation in glioblastoma (GBM) patients, its influence on tumour progression and radiotherapy response remains controversial. (2) Methods: We analysed patient data and used expression and cell biological analyses to assess effects of DEXA on GBM cells. We tested the efficacy of tyrosine kinase inhibitors in vitro and in vivo. (3) Results: We confirm in our patient cohort that administration of DEXA correlates with worse overall survival and shorter time to relapse. In GBM cells and glioma stem-like cells (GSCs) DEXA down-regulates genes controlling G2/M and mitotic-spindle checkpoints, and it enables cells to override the spindle assembly checkpoint (SAC). Concurrently, DEXA up-regulates Platelet Derived Growth Factor Receptor (PDGFR) signalling, which stimulates expression of anti-apoptotic regulators BCL2L1 and MCL1, required for survival during extended mitosis. Importantly, the protective potential of DEXA is dependent on intact tyrosine kinase signalling and ponatinib, sunitinib and dasatinib, all effectively overcome the radio-protective and pro-proliferative activity of DEXA. Moreover, we discovered that DEXA-induced signalling creates a therapeutic vulnerability for sunitinib in GSCs and GBM cells in vitro and in vivo. (4) Conclusions: Our results reveal a novel DEXA-induced mechanism in GBM cells and provide a rationale for revisiting the use of tyrosine kinase inhibitors for the treatment of GBM.

Indexed as

dexamethasoneglioblastomamitosis checkpointPDGFRsunitinib

Identifiers

PMID33478100
PMCPMC7836009
OpenAlexW3125225606

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.