Evidence map›Paper›PMID 27395057›Full record

ArticlePathology oncology research : POR2017

Region Specific Differences of Claudin-5 Expression in Pediatric Intracranial Ependymomas: Potential Prognostic Role in Supratentorial Cases.

József Virág, Christine Haberler, Gábor Baksa, Violetta Piurkó, Zita Hegedüs, Lilla Reiniger, Katalin Bálint, Monika Chocholous, András Kiss, Gábor Lotz and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Pathology oncology research : POR, 2017. 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
0.5field-weighted citation impact, top 26% 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. 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

14 authors at 3 institutions in 2 countries.

József Virág2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Christine HaberlerInstitute of Neuropathology, Medical University of Vienna, Vienna, Austria.
Gábor Baksa1st Department of Anatomy, Semmelweis University, Budapest, Hungary.
Violetta Piurkó2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
Zita Hegedüs2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
Lilla Reiniger1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Katalin Bálint1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Monika ChocholousDepartment of Pediatrics, Medical University of Vienna, Vienna, Austria.
András Kiss2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
Gábor Lotz2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
Tibor Glasz2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
Zsuzsa Schaff2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
Miklós Garami2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Balázs Hegedűs2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary. balazs.hegedus@meduniwien.ac.at.
Semmelweis University · HUMedical University of Vienna · ATHungarian Academy of Sciences · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ependymomas are common pediatric brain tumors that originate from the ependyma and characterized by poor prognosis due to frequent recurrence. However, the current WHO grading system fails to accurately predict outcome. In a retrospective study, we analyzed 54 intracranial pediatric ependymomas and found a significantly higher overall survival in supratentorial cases when compared to infratentorial tumors. Next we performed region-specific immunohistochemical analysis of the ependyma in neonatal and adult ependyma from the central canal of spinal cord to the choroid plexus of lateral ventricles for components of cell-cell junctions including cadherins, claudins and occludin. We found robust claudin-5 expression in the choroid plexus epithelia but not in other compartments of the ependyma. Ultrastructural studies demonstrated distinct regional differences in cell-cell junction organization. Surprisingly, we found that 9 out of 20 supratentorial but not infratentorial ependymomas expressed high levels of the brain endothelial tight junction component claudin-5 in tumor cells. Importantly, we observed an increased overall survival in claudin-5 expressing supratentorial ependymoma. Our data indicates that claudin-5 expressing ependymomas may follow a distinct course of disease. The assessment of claudin-5 expression in ependymoma has the potential to become a useful prognostic marker in this pediatric malignancy.

Indexed as

AdolescentBrain NeoplasmsChildChild, PreschoolClaudin-5EpendymomaFemaleHumansInfantInfratentorial NeoplasmsMaleNeoplasm Recurrence, LocalPrognosisRetrospective StudiesClaudin-5Choroid plexus epitheliumClaudin-5EpendymomaPrognosisSupratentorialTight junction

Identifiers

PMID27395057
PMCPMC5371650
OpenAlexW2470829610

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.