Evidence map›Paper›PMID 41420301›Full record

ArticleCancer reports (Hoboken, N.J.)2025

Fuelling Neuroblastoma: Genomic Analysis of Ketolytic and Glycolytic Gene Expression in Relation to MYCN Oncogene Amplification, Stage and Prognosis.

Joseph W Molloy, Karl Keogh, Mary-Kate McLoughlin, Lauren Devitt, David Lee, Eric Downer, David Robert Grimes, Denis Barry

Abstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Joseph W MolloyDiscipline of Anatomy, School of Medicine, Trinity College Dublin, Dublin, Ireland.ORCID 0009-0005-3467-9554
Karl KeoghDiscipline of Anatomy, School of Medicine, Trinity College Dublin, Dublin, Ireland.ORCID 0009-0005-9898-4996
Mary-Kate McLoughlinDiscipline of Anatomy, School of Medicine, Trinity College Dublin, Dublin, Ireland.
Lauren DevittDiscipline of Anatomy, School of Medicine, Trinity College Dublin, Dublin, Ireland.
David LeeDiscipline of Anatomy, School of Medicine, Trinity College Dublin, Dublin, Ireland.
Eric DownerDiscipline of Physiology, School of Medicine, Trinity College Dublin, Dublin, Ireland.ORCID 0000-0002-6012-2291
David Robert GrimesDiscipline of Public Health and Primary Care, School of Medicine, Trinity College Dublin, Dublin, Ireland.
Denis BarryDiscipline of Anatomy, School of Medicine, Trinity College Dublin, Dublin, Ireland.ORCID 0000-0002-6716-4275

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeuroblastoma (NB) is a childhood cancer of the sympathetic nervous system, and its prognosis is poor. NB cells undergo transcriptional changes to utilise aerobic glycolysis as their primary metabolic pathway, which provides an immediate source of ATP to meet high biosynthetic demands. Alternative metabolic fuel inputs, including ketone bodies which require oxidative phosphorylation, may impact the proliferative capacity of NB.

aimsIn this exploratory study, the expression of glycolytic and ketolytic genes in the context of MYCN oncogene amplification, tumour staging 1-4 and Kaplan-Meier survivability was investigated using the R2: Genomics analysis and visualisation platform (http://r2.amc.nl), database. METHODS AND

resultsThree NB genomics datasets were assessed in the R2 platform and further analysed in GraphPad Prism to investigate the relationships between glycolytic and ketolytic gene expression and prognosis. Glycolytic gene expression is increased in MYCN amplified, metastatic tumours and is associated with worse event free survival. Ketolytic gene expression is lower in metastatic tumours and is associated with better event free survivability. The glycolytic gene expression profile of NB suggests that elevated levels correlate with a low probability of survival. Ketolytic gene expression patterns suggest a decreased reliance for ketolytic energy, which may be exploited to slow tumourigenic growth.

conclusionsThis study validates glycolytic and ketolytic gene expression profiles in metastatic and MYCN amplified NB tumours and through conditional analysis suggests the potential use of these genes in prognosis prediction. Furthermore, the study highlights the reliability and utility of genomic databases as oncogenomic tools for NB research.

Indexed as

Biomarkers, TumorGlycolysisNeuroblastomaN-Myc Proto-Oncogene ProteinGene AmplificationGene Expression ProfilingGene Expression Regulation, NeoplasticGenomicsHumansKaplan-Meier EstimateNeoplasm StagingPrognosisBiomarkers, TumorMYCN protein, humanN-Myc Proto-Oncogene Proteingenomicsglycolysisketolysismetabolismneuroblastoma

Identifiers

PMID41420301
PMCPMC12717149

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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.