Evidence map›Paper›PMID 23108408›Full record

ArticleOncogene2013

miRNA-145 is downregulated in atypical and anaplastic meningiomas and negatively regulates motility and proliferation of meningioma cells.

N Kliese, P Gobrecht, D Pachow, N Andrae, A Wilisch-Neumann, E Kirches, M Riek-Burchardt, F Angenstein, G Reifenberger, M J Riemenschneider and 4 more

Open access · bronzeAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in Oncogene, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 2 pooled it
3.5field-weighted citation impact, top 8% 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, 2 syntheses or guidelines pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. The Epigenetic Landscape of Meningiomas.Advances in experimental medicine and biology · 2023
    Article
  13. Brain Invasion and Trends in Molecular Research on Meningioma.Brain tumor research and treatment · 2023
    Review
  14. Review
  15. Molecular neuropathology of brain-invasive meningiomas.Brain pathology (Zurich, Switzerland) · 2022
    Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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

14 authors at 7 institutions in 2 countries.

N KlieseInstitute of Neuropathology, Otto-von-Guericke University, Magdeburg, Germany.
P Gobrecht
D Pachow
N Andrae
A Wilisch-Neumann
E Kirches
M Riek-Burchardt
F Angenstein
G Reifenberger
M J Riemenschneider
E Meese
D Panayotova-Dimitrova
D H Gutmann
C Mawrin
Otto-von-Guericke University Magdeburg · DELeibniz Institute for Neurobiology · DEHeidelberg University · DEHeinrich Heine University Düsseldorf · DESaarland University · DEUniversity Hospital Regensburg · DEWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Meningiomas are frequent, mostly benign intracranial or spinal tumors. A small subset of meningiomas is characterized by histological features of atypia or anaplasia that are associated with more aggressive biological behavior resulting in increased morbidity and mortality. Infiltration into the adjacent brain tissue is a major factor linked to higher recurrence rates. The molecular mechanisms of progression, including brain invasion are still poorly understood. We have studied the role of micro-RNA 145 (miR-145) in meningiomas and detected significantly reduced miR-145 expression in atypical and anaplastic tumors as compared with benign meningiomas. Overexpression of miR-145 in IOMM-Lee meningioma cells resulted in reduced proliferation, increased sensitivity to apoptosis, reduced anchorage-independent growth and reduction of orthotopic tumor growth in nude mice as compared with control cells. Moreover, meningioma cells with high miR-145 levels had impaired migratory and invasive potential in vitro and in vivo. PCR-array studies of miR145-overexpressing cells suggested that collagen type V alpha (COL5A1) expression is downregulated by miR-145 overexpression. Accordingly, COL5A1 expression was significantly upregulated in atypical and anaplastic meningiomas. Collectively, our data indicate an important anti-migratory and anti-proliferative function of miR-145 in meningiomas.

Indexed as

AnimalsCell AdhesionCell DifferentiationCell DivisionCell MovementCollagen Type VDown-RegulationHumansMeningeal NeoplasmsMeningiomaMiceMice, NudeMicroRNAsNeoplasm GradingNeoplasm InvasivenessNeoplasm ProteinsCollagen Type VMicroRNAsMIRN145 microRNA, humanmirnlet7 microRNA, humanNeoplasm ProteinsRNA, Neoplasm

Identifiers

PMID23108408
OpenAlexW1976899677

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.