Evidence map›Paper›PMID 40836108›Full record

ArticlePediatric research2026

Circulating miRNAs as potential liquid biomarkers for pediatric gliomas.

Dikla Rogachevsky, Michal Yalon, Amos Toren, Ruty Mehrian-Shai

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Article in Pediatric research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Dikla RogachevskyFaculty of Medical and Health Sciences, Tel-Aviv University, Tel Aviv, Israel.
Michal YalonPediatric Hemato-Oncology, Sheba Medical Center, Tel Ha'shomer, Israel.
Amos TorenFaculty of Medical and Health Sciences, Tel-Aviv University, Tel Aviv, Israel. Amos.Toren@sheba.health.gov.il.
Ruty Mehrian-ShaiPediatric Hemato-Oncology, Sheba Medical Center, Tel Ha'shomer, Israel. Rutyshai@gmail.com.ORCID http://orcid.org/0000-0003-3961-0693

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCurrent diagnostic and monitoring of pediatric brain tumors rely on invasive tissue biopsies and imaging, highlighting the need for non-invasive alternatives. For that matter, liquid biopsy is a promising method. This pilot study investigated the potential of circulating miRNAs to serve as non-invasive biomarkers of pediatric glioma tumors.

methodsThe levels of mir-182-5p, mir-10b-5p, mir-106b-3p, mir-25-3p, and mir-21-5p were quantified in plasma samples from 68 pediatric gliomas patients and 12 Healthy controls using Real-time PCR. The results were assessed by differential and ROC curve analysis. Additionally, the involvement of mir-182-5p in pediatric high-grade gliomas aggressiveness was examined by functional studies using two cellular models.

resultsAll five circulating miRNAs demonstrated increased levels in pediatric glioma patients compared to HCs, significant correlation with Gliomas, and differential expression between various glioma subtypes. These miRNAs presented potential diagnostic discrimination between HCs and pediatric gliomas, as well as between different glioma subgroups. mir-182-5p showed the highest correlation to glioma and induction of migration as well as invasion ability of pediatric diffuse high-grade glioma 4 (pHGG-4) cells in vitro.

conclusionsOur findings present circulating miRNAs as promising biomarkers and treatment targets that, with further research, may be clinically utilized for monitoring pediatric glioma tumors. IMPACT: This study demonstrates the potential of circulating miRNAs as valuable biomarkers for pediatric glioma detection and monitoring. Five examined circulating miRNAs were differentially expressed in pediatric glioma patients compared to controls. These miRNAs were correlated with glioma and could distinguish healthy from gliomas patients. Statistical analysis suggested these miRNAs may also distinguish between various glioma subtypes. Inhibition of the most promising circulating miRNA, miR-182-5p, decreased migration ability and invasiveness of pediatric high-grade glioma IV cells. In the future, the miRNAs studied could have applications as biomarkers for clinical management and treatment targets.

Indexed as

Biomarkers, TumorBrain NeoplasmsCirculating MicroRNAGliomaMicroRNAsAdolescentCase-Control StudiesCell Line, TumorCell MovementChildChild, PreschoolFemaleGene Expression Regulation, NeoplasticHumansInfantLiquid BiopsyBiomarkers, TumorCirculating MicroRNAMicroRNAs

Identifiers

PMID40836108
PMCPMC13021524

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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.