Evidence map›Paper›PMID 36292985›Full record

ArticleInternational journal of molecular sciences2022

Phenotypical Flexibility of the EGFRvIII-Positive Glioblastoma Cell Line and the Multidirectional Influence of TGFβ and EGF on These Cells-EGFRvIII Appears as a Weak Oncogene.

Aneta Włodarczyk, Cezary Tręda, Adrianna Rutkowska, Dagmara Grot, Weronika Dobrewa, Amelia Kierasińska, Marta Węgierska, Tomasz Wasiak, Tadeusz Strózik, Piotr Rieske and 1 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
0.8field-weighted citation impact, top 27% 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, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. 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

11 authors at 1 institution in 1 country.

Aneta WłodarczykDepartment of Tumor Biology, Medical University of Lodz, Zeligowskiego 7/9 St., 90-752 Lodz, Poland.ORCID 0000-0002-9390-5639
Cezary TrędaDepartment of Tumor Biology, Medical University of Lodz, Zeligowskiego 7/9 St., 90-752 Lodz, Poland.
Adrianna RutkowskaDepartment of Tumor Biology, Medical University of Lodz, Zeligowskiego 7/9 St., 90-752 Lodz, Poland.ORCID 0000-0002-0973-6052
Dagmara GrotDepartment of Tumor Biology, Medical University of Lodz, Zeligowskiego 7/9 St., 90-752 Lodz, Poland.ORCID 0000-0002-3588-9140
Weronika DobrewaDepartment of Tumor Biology, Medical University of Lodz, Zeligowskiego 7/9 St., 90-752 Lodz, Poland.ORCID 0000-0001-8066-3303
Amelia KierasińskaDepartment of Tumor Biology, Medical University of Lodz, Zeligowskiego 7/9 St., 90-752 Lodz, Poland.
Marta WęgierskaDepartment of Tumor Biology, Medical University of Lodz, Zeligowskiego 7/9 St., 90-752 Lodz, Poland.
Tomasz WasiakDepartment of Molecular Biology, Medical University of Lodz, Zeligowskiego 7/9 St., 90-752 Lodz, Poland.
Tadeusz StrózikDepartment of Molecular Biology, Medical University of Lodz, Zeligowskiego 7/9 St., 90-752 Lodz, Poland.
Piotr RieskeDepartment of Tumor Biology, Medical University of Lodz, Zeligowskiego 7/9 St., 90-752 Lodz, Poland.ORCID 0000-0002-2970-0970
Ewelina Stoczyńska-FidelusDepartment of Tumor Biology, Medical University of Lodz, Zeligowskiego 7/9 St., 90-752 Lodz, Poland.
Medical University of Lodz · PL

Funding

National Science Center Grant 2019/35/B/NZ3/03577
6 · The paper itself

Abstract

backgroundThe biological role of EGFRvIII (epidermal growth factor receptor variant three) remains unclear.

methodsThree glioblastoma DK-MG sublines were tested with EGF (epidermal growth factor) and TGFβ (transforming growth factor β). Sublines were characterized by an increased percentage of EGFRvIII-positive cells and doubling time (DK-MG

resultsThe overexpression of exoEGFRvIII in DK-MG

conclusionsThe roles of TGFβ and EGF in the EGFRvIII context remain unclear. EGFRvIII appears as a weak oncogene and not a marker of GSC (glioma stem cells). Hence, it may not be a proper target for CAR-T (chimeric antigen receptor T cells).

Indexed as

GlioblastomaReceptors, Chimeric AntigenCell Line, TumorEpidermal Growth FactorErbB ReceptorsExtracellular Signal-Regulated MAP KinasesHumansOncogenesProto-Oncogene Proteins c-aktRNA, MessengerTranscription FactorsTransforming Growth Factor betaEpidermal Growth Factorepidermal growth factor receptor VIIIErbB ReceptorsExtracellular Signal-Regulated MAP KinasesProto-Oncogene Proteins c-aktReceptors, Chimeric AntigenRNA, MessengerTranscription FactorsTransforming Growth Factor betaapoptosisEGFRvIIIEMT-like phenomenonGBsenescenceTGFβ

Identifiers

PMID36292985
PMCPMC9603514
OpenAlexW4304689717

What Socratic 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 Socratic graph.