Evidence map›Paper›PMID 23291781›Full record

ArticleActa neuropathologica2013

DNA methylation profiling of medulloblastoma allows robust subclassification and improved outcome prediction using formalin-fixed biopsies.

Edward C Schwalbe, Daniel Williamson, Janet C Lindsey, Dolores Hamilton, Sarra L Ryan, Hisham Megahed, Miklós Garami, Peter Hauser, Bożena Dembowska-Baginska, Danuta Perek and 6 more

Abstract read
In one paragraph

Article in Acta neuropathologica, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed, 1 pooled it
6.3field-weighted citation impact, top 3% 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

94 citing papers in PubMed, 1 synthesis or guideline pooled it, 172 citations in OpenAlex.

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  9. From developmental origins to relapse: molecular and therapeutic insights in medulloblastoma.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
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34 more citing papers are in PubMed but not listed here.

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

16 authors at 8 institutions in 5 countries.

Edward C SchwalbeNorthern Institute for Cancer Research, Newcastle University, Sir James Spence Institute Level 5, Royal Victoria Infirmary, Newcastle upon Tyne, NE1 4LP, UK.
Daniel Williamson
Janet C Lindsey
Dolores Hamilton
Sarra L Ryan
Hisham Megahed
Miklós Garami
Peter Hauser
Bożena Dembowska-Baginska
Danuta Perek
Paul A Northcott
Michael D Taylor
Roger E Taylor
David W Ellison
Simon Bailey
Steven C Clifford
Newcastle University · GBRoyal Victoria Infirmary · GBChildren's Memorial Health Institute · PLSemmelweis University · HUHospital for Sick Children · CASickKids Foundation · CASingleton Hospital · GBSt. Jude Children's Research Hospital · US

Funding

Cancer Research UK 13457Cancer Research UK A13457
6 · The paper itself

Abstract

Molecular subclassification is rapidly informing the clinical management of medulloblastoma. However, the disease remains associated with poor outcomes and therapy-associated late effects, and the majority of patients are not characterized by a validated prognostic biomarker. Here, we investigated the potential of epigenetic DNA methylation for disease subclassification, particularly in formalin-fixed biopsies, and to identify biomarkers for improved therapeutic individualization. Tumor DNA methylation profiles were assessed, alongside molecular and clinical disease features, in 230 patients primarily from the SIOP-UKCCSG PNET3 clinical trial. We demonstrate by cross-validation in frozen training and formalin-fixed test sets that medulloblastoma comprises four robust DNA methylation subgroups (termed WNT, SHH, G3 and G4), highly related to their transcriptomic counterparts, and which display distinct molecular, clinical and pathological disease characteristics. WNT patients displayed an expected favorable prognosis, while outcomes for SHH, G3 and G4 were equivalent in our cohort. MXI1 and IL8 methylation were identified as novel independent high-risk biomarkers in cross-validated survival models of non-WNT patients, and were validated using non-array methods. Incorporation of MXI1 and IL8 into current survival models significantly improved the assignment of disease risk; 46 % of patients could be classified as 'favorable risk' (>90 % survival) compared to 13 % using current models, while the high-risk group was reduced from 30 to 16 %. DNA methylation profiling enables the robust subclassification of four disease subgroups in frozen and routinely collected/archival formalin-fixed biopsy material, and the incorporation of DNA methylation biomarkers can significantly improve disease-risk stratification. These findings have important implications for future risk-adapted clinical disease management.

Indexed as

DNA MethylationFormaldehydeAdolescentAdultBasic Helix-Loop-Helix ProteinsBiomarkers, TumorBiopsyCerebellar NeoplasmsChildChild, PreschoolChromosomes, Human, Pair 17Cohort StudiesComputational BiologyDNA FingerprintingFemaleFrozen SectionsBasic Helix-Loop-Helix ProteinsBiomarkers, TumorCXCL8 protein, humanFormaldehydeHedgehog ProteinsInterleukin-8MXI1 protein, humanProto-Oncogene Proteins c-mycSHH protein, humanTumor Suppressor Proteins

Identifiers

PMID23291781
PMCPMC4313078
OpenAlexW2337433062

What OpenQuestion holds

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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.