Evidence map›Paper›PMID 41033792›Full record

ArticleNeuropathology and applied neurobiology2025

Use of DNA Methylation Profiling as a Molecular Classification Tool for Paediatric Central Nervous System Tumours: A Middle-Income Country Population-Based Study.

Mayara F Euzébio, Felipe L T Silva, Iva L Hoffmann, Juliana S Ruas, Larissa Akemi Kido, Dieila G de Lima, Luciano Queiroz, Izilda A Cardinalli, Ana Luiza Seidinger, Suelen Nascimento and 5 more

Abstract read
In one paragraph

Article in Neuropathology and applied neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

15 authors.

Mayara F EuzébioResearch Center, Boldrini Children's Center, Campinas, São Paulo, Brazil.ORCID 0000-0003-2627-2576
Felipe L T SilvaResearch Center, Boldrini Children's Center, Campinas, São Paulo, Brazil.ORCID 0000-0003-4292-0027
Iva L HoffmannBoldrini Children's Centre, Campinas, São Paulo, Brazil.
Juliana S RuasResearch Center, Boldrini Children's Center, Campinas, São Paulo, Brazil.ORCID 0000-0002-5967-5235
Larissa Akemi KidoResearch Center, Boldrini Children's Center, Campinas, São Paulo, Brazil.ORCID 0000-0002-3653-8035
Dieila G de LimaResearch Center, Boldrini Children's Center, Campinas, São Paulo, Brazil.ORCID 0000-0002-5163-6047
Luciano QueirozBoldrini Children's Centre, Campinas, São Paulo, Brazil.
Izilda A CardinalliBoldrini Children's Centre, Campinas, São Paulo, Brazil.
Ana Luiza SeidingerResearch Center, Boldrini Children's Center, Campinas, São Paulo, Brazil.ORCID 0000-0002-9023-4649
Suelen NascimentoBoldrini Children's Centre, Campinas, São Paulo, Brazil.
Helder TedeschiBoldrini Children's Centre, Campinas, São Paulo, Brazil.
Renato D PugaResearch Center, Boldrini Children's Center, Campinas, São Paulo, Brazil.ORCID 0000-0002-6366-0765
Priscila Pini Zenatti SalesResearch Center, Boldrini Children's Center, Campinas, São Paulo, Brazil.ORCID 0000-0002-8662-7458
Patricia Y JottaResearch Center, Boldrini Children's Center, Campinas, São Paulo, Brazil.ORCID 0000-0001-9820-8210
Mariana MaschiettoResearch Center, Boldrini Children's Center, Campinas, São Paulo, Brazil.ORCID 0000-0003-2589-3186

Funding

PRONON 25000.012259/2019-42PRONON 25.000.069610/2015-43PRONON 25000.211368/2019-41
6 · The paper itself

Abstract

Paediatric central nervous system (CNS) tumours are the second most common childhood malignancy and the leading cause of cancer-related mortality in this age group. Histopathological diagnosis can be challenging, particularly for rare or ambiguous tumours, and may result in misclassification. To evaluate the utility of DNA methylation profiling in a middle-income country, we performed the Infinium MethylationEPIC BeadChip (Illumina) on tumours from 182 paediatric patients treated at a reference centre for paediatric oncology in Campinas, state of São Paulo, Brazil. Data were analysed using the DKFZ/Heidelberg CNS tumour classifier (v12.8). After excluding control tissue, 163 samples (89.6%) were suitable for classification; 135 (74.2%) achieved a calibrated score ≥ 0.9 and were assigned to a methylation class family. Methylation profiling resulted in a tumour subtype for 88 cases (65.7%) and changed the diagnosis in 28 cases (20.9%), identifying several rare tumour subtypes that were identified solely through methylation analysis, confirming the value of this method in improving diagnostic accuracy. This study highlights the utility of DNA methylation profiling for paediatric CNS tumours in a resource-limited setting and provides a cohort from an underrepresented middle-income population to international molecular databases.

Indexed as

Central Nervous System NeoplasmsDeveloping CountriesDNA MethylationGliomaBrazilCancer Care FacilitiesChildChild, PreschoolFemaleHumansInfantMaleDNA methylation profilingmiddle‐income countriesmolecular classificationmolecular tumour subtypespaediatric CNS tumours

Identifiers

PMID41033792
PMCPMC12488389

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.