Evidence map›Paper›PMID 37907716›Full record

ArticleJournal of neuro-oncology2023

Decreased eukaryotic initiation factors expression upon temozolomide treatment-potential novel implications for eIFs in glioma therapy.

Stefanie Krassnig, Stefan L Leber, Andrea Orthmann, Nicole Golob-Schwarzl, Heinrich Johann Huber, Christina Wohlrab, Christina Skofler, Mirjam Pennauer, Andrea Raicht, Anna Maria Birkl-Toeglhofer and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuro-oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
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

20 authors at 6 institutions in 4 countries.

Stefanie Krassnig *Diagnostic & Research Center for Molecular BioMedicine, Department of Neuropathology, Institute of Pathology, Medical University of Graz, Graz, Austria.
Stefan L Leber *Diagnostic & Research Center for Molecular BioMedicine, Department of Neuropathology, Institute of Pathology, Medical University of Graz, Graz, Austria.
Andrea OrthmannEPO Berlin Buch GmbH, Berlin, Germany.
Nicole Golob-SchwarzlDiagnostic & Research Center for Molecular BioMedicine, Department of Neuropathology, Institute of Pathology, Medical University of Graz, Graz, Austria.
Heinrich Johann HuberDrug Discovery Sciences, Dr. Boehringer Gasse 5-11 A-1121, Boehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Christina WohlrabDiagnostic & Research Center for Molecular BioMedicine, Department of Neuropathology, Institute of Pathology, Medical University of Graz, Graz, Austria.
Christina SkoflerDiagnostic & Research Center for Molecular BioMedicine, Department of Neuropathology, Institute of Pathology, Medical University of Graz, Graz, Austria.
Mirjam PennauerDiagnostic & Research Center for Molecular BioMedicine, Department of Neuropathology, Institute of Pathology, Medical University of Graz, Graz, Austria.
Andrea RaichtDivision of Paediatric Haematology and Oncology, Department of Paediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
Anna Maria Birkl-ToeglhoferDiagnostic & Research Center for Molecular BioMedicine, Department of Neuropathology, Institute of Pathology, Medical University of Graz, Graz, Austria.
Michael NaumannInstitute of Experimental Internal Medicine, Otto Von Guericke University, Magdeburg, Germany.
Kariem Mahdy-AliDepartment of Neurosurgery, Medical University of Graz, Graz, Austria.
Gord von CampeDepartment of Neurosurgery, Medical University of Graz, Graz, Austria.
Marlene LeoniDiagnostic & Research Center for Molecular BioMedicine, Department of Neuropathology, Institute of Pathology, Medical University of Graz, Graz, Austria.
Joshua AlcanizEPO Berlin Buch GmbH, Berlin, Germany.
Jens HoffmannEPO Berlin Buch GmbH, Berlin, Germany.
Thomas WälchliGroup of CNS Angiogenesis and Neurovascular Link, Neuroscience Center Zurich, Division of Neurosurgery, University and University Hospital Zurich, Zurich, Switzerland.
Serge WeisDivision of Neuropathology, Kepler University Hospital, Johannes Kepler University, Neuromed Campus, Linz, Austria.
Martin Benesch *Division of Paediatric Haematology and Oncology, Department of Paediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
Johannes Haybaeck *Diagnostic & Research Center for Molecular BioMedicine, Department of Neuropathology, Institute of Pathology, Medical University of Graz, Graz, Austria. johannes.Haybaeck@tyrolpath.at.
Medical University of Graz · ATBoehringer Ingelheim (Austria) · ATCenter For Biomarker Research In Medicine · ATOntario Brain Institute · CAOtto-von-Guericke University Magdeburg · DEUniversität Innsbruck · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSince glioma therapy is currently still limited until today, new treatment options for this heterogeneous group of tumours are of great interest. Eukaryotic initiation factors (eIFs) are altered in various cancer entities, including gliomas. The purpose of our study was to evaluate the potential of eIFs as novel targets in glioma treatment.

methodsWe evaluated eIF protein expression and regulation in 22 glioblastoma patient-derived xenografts (GBM PDX) after treatment with established cytostatics and with regards to mutation profile analyses of GBM PDX.

resultsWe observed decreased expression of several eIFs upon temozolomide (TMZ) treatment independent from the phosphatidylinositol 3-kinase (PI3K)/ AKT/ mammalian target of the rapamycin (mTOR) signalling pathway. These effects of TMZ treatment were not present in TMZ-resistant PDX. Combination therapy of regorafenib and TMZ re- established the eIF/AKT/mTOR axis.

conclusionOur study provides novel insights into chemotherapeutic effects on eIF regulation in gliomas and suggests that eIFs are interesting candidates for future research to improve glioma therapy.

Indexed as

Brain NeoplasmsGlioblastomaGliomaCell Line, TumorDacarbazineHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTemozolomideTOR Serine-Threonine KinasesDacarbazinePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTemozolomideTOR Serine-Threonine KinasesAstrocytomaEukaryotic initiation factorsGliomaGlioma therapyTemozolomide

Identifiers

PMID37907716
PMCPMC10638187
OpenAlexW4388038425

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.