Evidence map›Paper›PMID 20607354›Full record

ArticleJournal of neuro-oncology2011

Low-level copy number changes of MYC genes have a prognostic impact in medulloblastoma.

Karel Zitterbart, Hana Filkova, Lenka Tomasikova, Eva Necesalova, Iva Zambo, Dagmar Kantorova, Iva Slamova, Vladimira Vranova, Dita Zezulkova, Martina Pesakova and 4 more

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Article in Journal of neuro-oncology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. The Prognostic Value of Amplification of theDiseases (Basel, Switzerland) · 2025
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  12. A contemporary review of molecular candidates for the development and treatment of childhood medulloblastoma.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2013
    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

14 authors at 3 institutions in 1 country.

Karel ZitterbartDepartment of Pediatric Oncology, University Hospital Brno, Masaryk University, Cernopolni 9, 613 00 Brno, Czech Republic. kzitter@med.muni.cz
Hana Filkova
Lenka Tomasikova
Eva Necesalova
Iva Zambo
Dagmar Kantorova
Iva Slamova
Vladimira Vranova
Dita Zezulkova
Martina Pesakova
Zdenek Pavelka
Renata Veselska
Petr Kuglik
Jaroslav Sterba
University Hospital Brno · CZMasaryk University · CZSt. Anne's University Hospital Brno · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-level amplifications of MYC genes are associated with poor outcomes in childhood medulloblastoma (MB). However, the occurrence of MYCN and MYCC copy number increases below the intense amplification pattern is rarely reported, and its clinical impact has not yet been determined. Here, we describe this phenomenon and its prognostic significance in a cohort of 29 MB patients. Using interphase fluorescence in situ hybridization (I-FISH), low-level copy number alterations, i.e. gain of MYCN, were shown in 5/27 (19%) samples, whereas amplification was revealed in only 1/27 (4%) samples. MYCC gain was revealed in 6/29 (21%) MB, while amplification was disclosed in only 2/29 (7%). Hyperploidy and co-incidence of gains in both MYC loci were frequently observed in samples with copy number aberrations. Survival analysis has clearly shown that MYC copy number increases are associated with lowered event-free survival and overall survival in MB. In the case of MYCN, this negative correlation was statistically significant. We conclude that limited numerical alterations in loci 2p24 (MYCN) and 8q24 (MYCC), as assessed by I-FISH, are present in MB with a higher frequency than high-level amplifications. Poor prognoses were observed in patients with copy number increases in MYC genes. Our data illustrate the importance of further investigations in multicenter trials to better refine the emerging genomic-based prognostic stratification in MB.

Indexed as

Gene AmplificationGene DosageAdolescentCerebellar NeoplasmsChildChild, PreschoolCohort StudiesFemaleHumansIn Situ Hybridization, FluorescenceInterphaseMaleMedulloblastomaN-Myc Proto-Oncogene ProteinNuclear ProteinsOncogene ProteinsMYCN protein, humanMYC protein, humanN-Myc Proto-Oncogene ProteinNuclear ProteinsOncogene ProteinsProto-Oncogene Proteins c-myc

Identifiers

PMID20607354
OpenAlexW1995427420

What OpenQuestion holds

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Registered trials

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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.