Evidence map›Paper›PMID 25146167›Full record

ArticleVirchows Archiv : an international journal of pathology2014

Complex interactions between the components of the PI3K/AKT/mTOR pathway, and with components of MAPK, JAK/STAT and Notch-1 pathways, indicate their involvement in meningioma development.

Elias A El-Habr, Georgia Levidou, Eleni-Andriana Trigka, Joanna Sakalidou, Christina Piperi, Ilenia Chatziandreou, Anastasia Spyropoulou, Rigas Soldatos, Georgia Tomara, Kalliopi Petraki and 8 more

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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Meningiomas in Rubinstein-Taybi syndrome: A case report and comprehensive review.Journal of neuropathology and experimental neurology · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. The Epigenetic Landscape of Meningiomas.Advances in experimental medicine and biology · 2023
    Article
  16. Cancers · 2022
    Article
  17. mTOR Signaling and Potential Therapeutic Targeting in Meningioma.International journal of molecular sciences · 2022
    Review
  18. Review
  19. Article
  20. Association of Single-Nucleotide Polymorphisms of Gab1 Gene with Susceptibility to Meningioma in a Northern Chinese Han Population.Medical science monitor : international medical journal of experimental and clinical research · 2021
    Article
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

18 authors at 5 institutions in 3 countries.

Elias A El-HabrFirst Department of Pathology, Laikon General Hospital, Athens University Medical School, 115 27, Athens, Greece, elhabere@yahoo.com.
Georgia Levidou
Eleni-Andriana Trigka
Joanna Sakalidou
Christina Piperi
Ilenia Chatziandreou
Anastasia Spyropoulou
Rigas Soldatos
Georgia Tomara
Kalliopi Petraki
Vassilis Samaras
Athanasios Zisakis
Vassilis Varsos
George Vrettakos
Efstathios Boviatsis
Efstratios Patsouris
Angelica A Saetta
Penelope Korkolopoulou
National and Kapodistrian University of Athens · GRHellenic Red Cross · GRMetropolitan Hospital · GRAthens State University · USRed Cross Hospital · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated the significance of PI3K/AKT/mTOR pathway and its interactions with MAPK, JAK/STAT and Notch pathways in meningioma progression. Paraffin-embedded tissue from 108 meningioma patients was analysed for the presence of mutations in PIK3CA and AKT1. These were correlated with the expression status of components of the PI3K/AKT/mTOR pathway, including p85α and p110γ subunits of PI3K, phosphorylated (p)-AKT, p-mTOR, p-p70S6K and p-4E-BP1, as well as of p-ERK1/2, p-STAT3 and Notch-1, clinicopathological data and patient survival. A mutation in PIK3CA or AKT1 was found in around 9 % of the cases. Higher grade meningiomas displayed higher nuclear expression of p-p70S6K; higher nuclear and cytoplasmic expression of p-4E-BP1 and of Notch-1; lower cytoplasmic expression of p85αPI3K, p-p70S6K and p-ERK1/2; and lower PTEN Histo-scores (H-scores). PTEN H-score was inversely correlated with recurrence probability. In univariate survival analysis, nuclear expression of p-4E-BP1 and absence of p-ERK1/2 expression portended adverse prognosis, whereas in multivariate survival analysis, p-ERK1/2 expression emerged as an independent favourable prognostic factor. Treatment of the human meningioma cell line HBL-52 with the PI3K inhibitor LY294002 resulted in reduction of p-AKT, p-p70S6K and p-ERK1/2 protein levels. The complex interactions established between components of the PI3K/AKT/mTOR pathway, or with components of the MAPK, JAK/STAT and Notch-1 pathways, appear to be essential for facilitating and fuelling meningioma progression.

Indexed as

Blotting, WesternBrain NeoplasmsCell Line, TumorDisease ProgressionFemaleHumansImmunohistochemistryJanus KinasesMaleMeningiomaMitogen-Activated Protein Kinase KinasesMutationPhosphatidylinositol 3-KinasesPrognosisProto-Oncogene Proteins c-aktReceptor, Notch1Janus KinasesMitogen-Activated Protein Kinase KinasesMTOR protein, humanNOTCH1 protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptor, Notch1STAT Transcription FactorsTOR Serine-Threonine Kinases

Identifiers

PMID25146167
OpenAlexW2010954587

What OpenQuestion holds

Textmetadata
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.