Evidence map›Paper›PMID 35163107›Full record

ReviewInternational journal of molecular sciences2022

Bilateral Meningioma: A Case Report and Review of the Literature.

Anja Bukovac, Hana Panić, Tomislava Mrgan, Nika Šlaus, Anja Kafka, Niko Njirić, Nives Pećina-Šlaus

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.7field-weighted citation impact, top 15% 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, 8 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 2 institutions in 1 country.

Anja BukovacLaboratory of Neuro-Oncology, Croatian Institute for Brain Research, School of Medicine, University of Zagreb, Šalata 12, 10000 Zagreb, Croatia.ORCID 0000-0001-6587-8314
Hana PanićSchool of Medicine, University of Zagreb, Šalata 3, 10000 Zagreb, Croatia.ORCID 0000-0001-8214-4953
Tomislava MrganSchool of Medicine, University of Zagreb, Šalata 3, 10000 Zagreb, Croatia.
Nika ŠlausSchool of Medicine, University of Zagreb, Šalata 3, 10000 Zagreb, Croatia.
Anja KafkaLaboratory of Neuro-Oncology, Croatian Institute for Brain Research, School of Medicine, University of Zagreb, Šalata 12, 10000 Zagreb, Croatia.
Niko NjirićDepartment of Neurosurgery, University Hospital Center "Zagreb", School of Medicine, University of Zagreb, Kišpatićeva 12, 10000 Zagreb, Croatia.
Nives Pećina-ŠlausLaboratory of Neuro-Oncology, Croatian Institute for Brain Research, School of Medicine, University of Zagreb, Šalata 12, 10000 Zagreb, Croatia.ORCID 0000-0002-3334-7671
University of Zagreb · HRUniversity Hospital Centre Zagreb · HR

Funding

European Union through the European Regional Development Fund GA KK01.1.1.01.0007
6 · The paper itself

Abstract

Here, we present a rarely seen example of bilateral meningiomas exhibiting different malignancy grades, I (meningothelial) and II (atypical), recorded in a 72-year-old patient. The presence of two separated lesions of different grades in a single patient can elucidate meningioma progression. To this end, the involvement of specific protein markers of epithelial to mesenchymal transition (EMT), the process responsible for progression, was tested in both tumors. Protein expression status of specific epithelial (E-cadherin) and mesenchymal markers (N-cadherin, SNAIL&SLUG and TWIST1) was investigated. Furthermore, markers that are connected to Wnt signaling pathway-beta-catenin, GSK3beta and DVL1-were also analyzed. For signs of neurofibromatosis and schwanomatosis genetic testing was performed. Immunohistochemistry evaluated by immunoreactivity score (IRS) was used to determine the signal strengths and proteins' location. Our results indicated that, in comparison to the grade I tumor, mesenchymal markers SNAIL and SLUG were upregulated in the atypical meningioma. TWIST1, beta-catenin and GSK3beta were upregulated in both grades, while E-cadherin was partially lost. A pronounced cadherin switch could not be established; however, N-cadherin showed widespread tissue presence. Genetic testing did not detect changes of

Indexed as

AgedBiomarkers, TumorFemaleGenetic TestingHumansMeningeal NeoplasmsMeningiomaBiomarkers, Tumorbeta-cateninbilateral meningiomaDVL1E-cadherinEMTGSK3betamultiple meningiomaN-cadherinSNAIL&SLUGTWIST1Wnt signaling

Identifiers

PMID35163107
PMCPMC8835044
OpenAlexW4206247179

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.