Evidence map›Paper›PMID 38662144›Full record

ArticleJournal of molecular neuroscience : MN2024

A Prognostic Methylation-Driven Two-Gene Signature in Medulloblastoma.

Gustavo Lovatto Michaelsen, Lívia Dos Reis Edinger da Silva, Douglas Silva de Lima, Mariane da Cunha Jaeger, André Tesainer Brunetto, Rodrigo Juliani Siqueira Dalmolin, Marialva Sinigaglia

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular neuroscience : MN, 2024. 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
0.4field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Genome-wide DNA methylation analysis of pediatric medulloblastomas from a Brazilian cohort: an exploratory study.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    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

7 authors at 4 institutions in 4 countries.

Gustavo Lovatto MichaelsenChildren's Cancer Institute, Porto Alegre, 90620-110, RS, Brazil.ORCID http://orcid.org/0000-0002-9433-0822
Lívia Dos Reis Edinger da SilvaChildren's Cancer Institute, Porto Alegre, 90620-110, RS, Brazil.
Douglas Silva de LimaChildren's Cancer Institute, Porto Alegre, 90620-110, RS, Brazil.
Mariane da Cunha JaegerChildren's Cancer Institute, Porto Alegre, 90620-110, RS, Brazil.ORCID http://orcid.org/0000-0002-3465-4083
André Tesainer BrunettoChildren's Cancer Institute, Porto Alegre, 90620-110, RS, Brazil.ORCID http://orcid.org/0000-0002-7958-1279
Rodrigo Juliani Siqueira DalmolinBioinformatics Multidisciplinary Environment-BioME, Digital Metropole Institute, Federal University of Rio Grande do Norte, Natal, 59076-550, RN, Brazil.ORCID http://orcid.org/0000-0002-1688-6155
Marialva SinigagliaChildren's Cancer Institute, Porto Alegre, 90620-110, RS, Brazil. msinigaglia@ici.ong.ORCID http://orcid.org/0000-0002-8324-6860
Cancer Research Institute of the Slovak Academy of Sciences · SKUniversidade Federal do Rio Grande do Norte · BRUniversidade Federal do Rio Grande do Sul · BRChildren's Oncology Group · CH

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 312305/2021-4National Council for Scientific and Technological Development (CNPq, MCTI, Brazil) 406484/2022-8 (INCT BioOncoPed)
6 · The paper itself

Abstract

Medulloblastoma (MB) is one of the most common pediatric brain tumors and it is estimated that one-third of patients will not achieve long-term survival. Conventional prognostic parameters have limited and unreliable correlations with MB outcome, presenting a major challenge for patients' clinical improvement. Acknowledging this issue, our aim was to build a gene signature and evaluate its potential as a new prognostic model for patients with the disease. In this study, we used six datasets totaling 1679 samples including RNA gene expression and DNA methylation data from primary MB as well as control samples from healthy cerebellum. We identified methylation-driven genes (MDGs) in MB, genes whose expression is correlated with their methylation. We employed LASSO regression, incorporating the MDGs as a parameter to develop the prognostic model. Through this approach, we derived a two-gene signature (GS-2) of candidate prognostic biomarkers for MB (CEMIP and NCBP3). Using a risk score model, we confirmed the GS-2 impact on overall survival (OS) with Kaplan-Meier analysis. We evaluated its robustness and accuracy with receiver operating characteristic curves predicting OS at 1, 3, and 5 years in multiple independent datasets. The GS-2 showed highly significant results as an independent prognostic biomarker compared to traditional MB markers. The methylation-regulated GS-2 risk score model can effectively classify patients with MB into high and low-risk, reinforcing the importance of this epigenetic modification in the disease. Such genes stand out as promising prognostic biomarkers with potential application for MB treatment.

Indexed as

Biomarkers, TumorCerebellar NeoplasmsDNA MethylationMedulloblastomaTranscriptomeChildChild, PreschoolFemaleHumansMalePrognosisBiomarkers, TumorDNA methylationMedulloblastomaPrecision medicinePrognostic biomarker

Identifiers

PMID38662144
OpenAlexW4395456017

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.