Evidence map›Paper›PMID 19908067›Full record

ArticleJournal of cancer research and clinical oncology2010

Genetic and protein changes of E-cadherin in meningiomas.

Nives Pećina-Slaus, Tamara Nikuseva Martić, Adam Jakov Deak, Martina Zeljko, Reno Hrasćan, Davor Tomas, Vesna Musani

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In one paragraph

Article in Journal of cancer research and clinical oncology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Mismatch Repair Pathway, Genome Stability and Cancer.Frontiers in molecular biosciences · 2020
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Immunohistochemical characterization of brain-invasive meningiomas.International journal of clinical and experimental pathology · 2014
    Article
  11. Merlin, the NF2 gene product.Pathology oncology research : POR · 2013
    Review
  12. Article
  13. Article
  14. Article
  15. 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

7 authors at 3 institutions in 1 country.

Nives Pećina-SlausCroatian Institute for Brain Research, School of Medicine, University of Zagreb, Croatia. nina@mef.hr
Tamara Nikuseva Martić
Adam Jakov Deak
Martina Zeljko
Reno Hrasćan
Davor Tomas
Vesna Musani
University of Zagreb · HRRudjer Boskovic Institute · HRSisters of Charity Hospital · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe molecular mechanisms and candidate genes involved in development of meningiomas still needs investigation and elucidation.

methodsIn the present study 60 meningiomas were analyzed regarding changes of tumor suppressor gene E-cadherin (CDH1), a component of adherens junction and an indirect modulator of the wnt signaling. Gene instability was tested by polymerase chain reaction/loss of heterozygosity (LOH) method. Protein expression was analyzed by immunohistochemistry.

resultsThe results of our analysis showed altogether 32% of samples with LOH of the CDH1 gene. Interestingly, another type of genomic instability was detected; replication error-positive samples (RER+). Three out of 28 heterozygous samples were RER+ (11%). The instability is the result of impaired cellular mismatch repair. Fibrous and angiomatous cases showed higher percent of genetic changes, 67 and 75%, respectively. Immunostaining showed that overall 73% of samples had downregulation of E-cadherin expression. Intense downregulation of E-cadherin was noticed in tumors with grades II and III. Five out of nine samples with LOH were accompanied with the downregulation of E-cadherin protein expression (56%). One RER+ sample had lower expression of E-cadherin. We noticed that 36.4% of samples with lower E-cadherin expression had beta-catenin located in the nucleus. Also, 75% of samples with genomic instabilities had beta-catenin in the nucleus. Our findings demonstrated that there is significant association between the genetic changes of CDH1 and the nuclear localization of beta-catenin protein (chi(2) = 5.25, df = 1, P < 0.022). Beta-catenin was progressively upregulated from meningothelial to atypical, while 60% of anaplastic showed upregulation and nuclear localization of the protein.

conclusionsOur results suggest that genetic instabilities of the E-cadherin gene have a role in meningioma development and progression. Detected microsatellite instability indicates that mismatch repair may also be targeted in meningioma.

Indexed as

Genomic InstabilityAdultAgedbeta CateninCadherinsFemaleHumansLoss of HeterozygosityMaleMeningeal NeoplasmsMeningiomaMiddle Agedbeta CateninCadherins

Identifiers

PMID19908067
PMCPMC11827954
OpenAlexW2030848083

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.