Evidence map›Paper›PMID 27390862›Full record

ArticlePloS one2016

Altered MicroRNA Expression Is Associated with Tumor Grade, Molecular Background and Outcome in Childhood Infratentorial Ependymoma.

Magdalena Zakrzewska, Wojciech Fendler, Krzysztof Zakrzewski, Beata Sikorska, Wiesława Grajkowska, Bożenna Dembowska-Bagińska, Iwona Filipek, Łukasz Stefańczyk, Paweł P Liberski

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.2field-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

18 citing papers in PubMed, 28 citations in OpenAlex.

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  8. mRNA and miRNA Expression Analyses of theInternational journal of molecular sciences · 2021
    Article
  9. MicroRNA Signature in Human Normal and Tumoral Neural Stem Cells.International journal of molecular sciences · 2019
    Review
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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

9 authors at 4 institutions in 1 country.

Magdalena ZakrzewskaDepartment of Molecular Pathology and Neuropathology, Medical University of Lodz, Lodz, Poland.
Wojciech FendlerDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Lodz, Poland.
Krzysztof ZakrzewskiDepartment of Neurosurgery, Polish Mother Memorial Hospital Research Institute, Lodz, Poland.
Beata SikorskaDepartment of Molecular Pathology and Neuropathology, Medical University of Lodz, Lodz, Poland.
Wiesława GrajkowskaDepartment of Pathology, Children's Memorial Health Institute, Warsaw, Poland.
Bożenna Dembowska-BagińskaDepartment of Pediatric Oncology, Children's Memorial Health Institute, Warsaw, Poland.
Iwona FilipekDepartment of Pediatric Oncology, Children's Memorial Health Institute, Warsaw, Poland.
Łukasz StefańczykThird Municipal Hospital in Lodz, Lodz, Poland.
Paweł P LiberskiDepartment of Molecular Pathology and Neuropathology, Medical University of Lodz, Lodz, Poland.
Medical University of Lodz · PLChildren's Memorial Health Institute · PLMossakowski Medical Research Institute, Polish Academy of Sciences · PLPolish Mother’s Memorial Hospital Research Institute · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEpendymal tumors are the third most common group of brain tumors in children, accounting for about 10% of all primary brain neoplasms. According to the current WHO classification, they comprise four entities with the most frequent ependymoma and anaplastic ependymoma. The most of pediatric tumors are located within the posterior fossa, with a tendency to infiltrate the vital brain structures. This limits surgical resection and poses a considerable clinical problem. Moreover, there are no appropriate outcome prognostic factors besides the extent of surgical resection. Despite definition of molecular subgroups, the majority of childhood ependymomas present a balanced genome, which makes it difficult to establish molecular prognostic factors.

methodsThe purpose of our study was to explore whether miRNA expression could be used as prognostic markers in pediatric infratentorial ependymomas. We also performed a mRNA expression pattern analysis of NELL2 and LAMA2 genes, with immunohistochemical illustrations of representative cases. The miRNA and mRNA expression was measured in 53 pediatric infratentorial ependymomas using a real-time quantitative PCR.

resultsThree miRNAs were shown to efficiently differentiate between grade II and III ependymomas: miR-17-5p, miR-19a-3p, and miR-106b-5p. Survival analysis showed that the probabilities of overall (p = 0.036) and event-free survival (p = 0.002) were reduced with higher than median miRNA expression levels of miR-17-5p. Using multivariate analysis adjusted for patient's age, sex, tumor grade and localization, we showed statistically significant associations with event-free survival (p = 0004) and borderline statistical significance with overall survival (p = 0.057) for miR-17-5p. Correlation analysis of miR-19a, miR-17-5p, miR-106b revealed that their expression levels were significantly correlated with EZH2 expression, suggested marker of PFA ependymomas. Furthermore, lower expression level of LAMA2 mRNA was shown to be associated with an increased risk of death in covariate-adjusted analyses.

conclusionsOur data provide a better understanding of pediatric ependymoma and suggests the presence of plausible molecular biomarkers connected with the outcome.

Indexed as

AdolescentBiomarkers, TumorBrain NeoplasmsChildChild, PreschoolDisease-Free SurvivalDNA, ComplementaryEpendymomaFemaleGene Expression Regulation, NeoplasticHumansImmunohistochemistryInfantInfratentorial NeoplasmsMaleMicroRNAsBiomarkers, TumorDNA, ComplementaryMicroRNAsMIRN106 microRNA, humanMIRN17 microRNA, humanMIRN19A microRNA, human

Identifiers

PMID27390862
PMCPMC4938415
OpenAlexW2462813763

What OpenQuestion holds

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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.