Evidence map›Paper›PMID 42816786›Full record

ArticleCancer reports (Hoboken, N.J.)2026

Deepening the Understanding of Platelet-Derived RNA as Biomarker for Glioblastoma Through GSEA, TDEA, and Elastic Net Regularization Analysis.

Anna Giczewska, Krzysztof Pastuszak, Leon van Hout, Edward Post, Jip Ramaker, Ken Zwaan, Anna Supernat, Bart A Westerman

Abstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Anna GiczewskaLaboratory of Translational Oncology, Intercollegiate Faculty of Biotechnology, University of Gdańsk and Medical University of Gdańsk, Gdańsk, Poland.ORCID https://orcid.org/0000-0003-0533-2453
Krzysztof PastuszakLaboratory of Translational Oncology, Intercollegiate Faculty of Biotechnology, University of Gdańsk and Medical University of Gdańsk, Gdańsk, Poland.ORCID https://orcid.org/0000-0002-5562-0114
Leon van HoutDepartment of Neurosurgery, Cancer Center Amsterdam, Amsterdam UMC Location VUMC, Amsterdam, the Netherlands.ORCID https://orcid.org/0009-0007-3040-6692
Edward PostDepartment of Neurosurgery, Cancer Center Amsterdam, Amsterdam UMC Location VUMC, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0002-4924-321X
Jip RamakerDepartment of Neurosurgery, Cancer Center Amsterdam, Amsterdam UMC Location VUMC, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0002-8090-1276
Ken ZwaanDepartment of Neurosurgery, Cancer Center Amsterdam, Amsterdam UMC Location VUMC, Amsterdam, the Netherlands.
Anna SupernatLaboratory of Translational Oncology, Intercollegiate Faculty of Biotechnology, University of Gdańsk and Medical University of Gdańsk, Gdańsk, Poland.ORCID https://orcid.org/0000-0002-3113-0540
Bart A WestermanDepartment of Neurosurgery, Cancer Center Amsterdam, Amsterdam UMC Location VUMC, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0002-9898-9616

Funding

Gdański Uniwersytet Medyczny MNISW 07/IDUB/2019/94Health~Holland Grants called AI-IMPACTToxicity-Atlas
6 · The paper itself

Abstract

backgroundGlioblastoma (GBM) is the most aggressive form of primary brain cancer. Blood platelets have emerged as biomarkers where their RNA expression pattern indicates a tumor's presence. Our study aimed to characterize these patterns to identify biological processes associated with GBM and to evaluate their potential as a non-invasive biomarker.

methodsWe analyzed platelet RNA-seq expression profiles from 84 GBM patients and 319 healthy individuals using two complementary analytical approaches of Gene Set Enrichment Analysis and Threshold-based Differential Expression Analysis with Elastic Net regularization. Together, these approaches may offer complementary perspectives on biological pathways associated with GBM and the descriptive functional annotation of a predictive platelet RNA gene signature, providing insight into platelet-tumor interactions.

resultsOur GSEA broad analysis highlighted platelet-related biological processes, including coagulation, wound healing, immune regulation, and cytoskeletal organization. The Elastic Net framework additionally suggested pathways related to immune activation, cell signaling, and protein folding. Overall, these findings may suggest that platelet-derived RNA not only has potential as a non-invasive biomarker but may also provide insight into the systemic biological processes associated with the GBM tumor microenvironment.

conclusionsOur data suggests that platelet-derived RNA may reflect biological processes associated with the GBM tumor microenvironment, where wound repair and immune-related processes may play important roles. Our findings provide a resource for further research into the mechanisms that may underlie the pathophysiology and progression of glioblastoma.

Indexed as

Biomarkers, TumorBlood PlateletsBrain NeoplasmsGlioblastomaRNACase-Control StudiesFemaleGene Expression Regulation, NeoplasticHumansTumor MicroenvironmentBiomarkers, TumorRNAbioinformaticsbiomarkersglioblastomapathway analysisplatelet RNA

Identifiers

PMID42816786
PMCPMC13627264

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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.