Evidence map›Paper›PMID 36361720›Full record

ArticleInternational journal of molecular sciences2022

Targeting Key Signaling Pathways in Glioblastoma Stem Cells for the Development of Efficient Chemo- and Immunotherapy.

Laureen P Helweg, Jonathan Storm, Kaya E Witte, Wiebke Schulten, Lennart Wrachtrup, Till Janotte, Angelika Kitke, Johannes F W Greiner, Cornelius Knabbe, Barbara Kaltschmidt and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 12 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

12 authors at 2 institutions in 1 country.

Laureen P HelwegDepartment of Cell Biology, University of Bielefeld, Universitätsstrasse 25, 33615 Bielefeld, Germany.ORCID 0000-0003-3520-0558
Jonathan StormDepartment of Cell Biology, University of Bielefeld, Universitätsstrasse 25, 33615 Bielefeld, Germany.
Kaya E WitteDepartment of Cell Biology, University of Bielefeld, Universitätsstrasse 25, 33615 Bielefeld, Germany.ORCID 0000-0001-9300-3355
Wiebke SchultenDepartment of Cell Biology, University of Bielefeld, Universitätsstrasse 25, 33615 Bielefeld, Germany.
Lennart WrachtrupDepartment of Cell Biology, University of Bielefeld, Universitätsstrasse 25, 33615 Bielefeld, Germany.
Till JanotteDepartment of Cell Biology, University of Bielefeld, Universitätsstrasse 25, 33615 Bielefeld, Germany.
Angelika KitkeDepartment of Cell Biology, University of Bielefeld, Universitätsstrasse 25, 33615 Bielefeld, Germany.
Johannes F W GreinerDepartment of Cell Biology, University of Bielefeld, Universitätsstrasse 25, 33615 Bielefeld, Germany.ORCID 0000-0002-0524-662X
Cornelius KnabbeForschungsverbund BioMedizin Bielefeld, OWL (FBMB e.V.), Maraweg 21, 33617 Bielefeld, Germany.
Barbara KaltschmidtDepartment of Cell Biology, University of Bielefeld, Universitätsstrasse 25, 33615 Bielefeld, Germany.
Matthias SimonForschungsverbund BioMedizin Bielefeld, OWL (FBMB e.V.), Maraweg 21, 33617 Bielefeld, Germany.
Christian KaltschmidtDepartment of Cell Biology, University of Bielefeld, Universitätsstrasse 25, 33615 Bielefeld, Germany.
Bielefeld University · DEHeart and Diabetes Center North Rhine-Westphalia · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the most aggressive and most common malignant brain tumor with poor patient survival despite therapeutic intervention. On the cellular level, GBM comprises a rare population of glioblastoma stem cells (GSCs), driving therapeutic resistance, invasion, and recurrence. GSCs have thus come into the focus of therapeutic strategies, although their targeting remains challenging. In the present study, we took advantage of three GSCs-populations recently established in our lab to investigate key signaling pathways and subsequent therapeutic strategies targeting GSCs. We observed that NF-κB, a crucial transcription factor in GBM progression, was expressed in all CD44

Indexed as

Brain NeoplasmsGlioblastomaCell Line, TumorHumansImmunotherapyNeoplastic Stem CellsNF-kappa BSignal TransductionNF-kappa Bcancer stem cellschemotherapyglioblastoma multiformeimmunotherapyMYCNF-κBNK-cells

Identifiers

PMID36361720
PMCPMC9659205
OpenAlexW4307281068

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.