Evidence map›Paper›PMID 41146060›Full record

ArticleBMC cancer2025

Study of plasma exosomal miRNAs as novel biomarkers for differentiating primary central nervous system lymphoma and glioblastoma.

Shan Lu, Lixia Xu, Yu Lan, Chen Wang, Lidong Mo, Hua Yan

Abstract read
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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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

5 citing papers in PubMed.

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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

6 authors.

Shan Lu *Huanhu Hospital Affiliated to Tianjin Medical University, Tianjin Medical University, Tianjin, 300070, China.
Lixia Xu *Huanhu Hospital Affiliated to Tianjin Medical University, Tianjin Medical University, Tianjin, 300070, China.
Yu Lan *Clinical College of Neurology, Neurosurgery, and Neurorehabilitation, Tianjin Medical University, Tianjin, 300070, China.
Chen WangHuanhu Hospital Affiliated to Tianjin Medical University, Tianjin Medical University, Tianjin, 300070, China.
Lidong MoHuanhu Hospital Affiliated to Tianjin Medical University, Tianjin Medical University, Tianjin, 300070, China.
Hua YanHuanhu Hospital Affiliated to Tianjin Medical University, Tianjin Medical University, Tianjin, 300070, China. yanhua20042007@sina.com.

Funding

Tianjin Health Research Project TJWJ2022QN059Tianjin Municipal Education Commission Scientific Research Project 2024KJ254
6 · The paper itself

Abstract

Preoperative diagnosis of the nature of PCNSL is crucial for distinguishing it from commonly confused intracranial gliomas, such as glioblastoma multiforme (GBM). The present research aims to sequence peripheral blood exosomal miRNAs from PCNSL and GBM patients, and to identify the discriminative miRNAs with high feasibility. Plasma exosomal RNAs were extracted, and miRNA sequencing was performed. The miRNAs with significant differences were validated by RT-qPCR. A total of 67 miRNAs were significantly different between the PCNSL and GBM groups. Twenty-seven PCNSL and 27 GBM patients were enrolled for the RT-qPCR validation of 10 selected differentially expressed miRNAs. The expression levels of plasma exosomal hsa-miR-148a-3p, hsa-let-7f-5p, hsa-miR-345-5p and hsa-miR-4433b-5p were upregulated in the PCNSL group compared with those in the GBM group (P = 0.019, P = 0.036, P = 0.009, and P = 0.001, respectively). The combined panel comprising hsa-miR-148a-3p, hsa-miR-345-5p, and hsa-miR-4433b-5p demonstrated significantly enhanced diagnostic performance, with an area under the ROC curve (AUC) of 0.791. Immunohistochemistry analysis revealed that the expression level of EGFR in PCNSL was significantly lower than that in GBM. Western blot and RT-qPCR analysis of EGFR expression levels in LN229 cells revealed that miR-148a-3p and miR-4433b-5p downregulated EGFR expression. The results of luciferase reporter assay showed that the relative luciferase activity of HEK293T cells transfected with EGFR-WT was notably suppressed by miR-4433b-5p (P < 0.001). In conclusion, the plasma exosomal hsa-miR-148a-3p, hsa-miR-345-5p, and hsa-miR-4433b-5p might be identified as novel biomarkers for differentiating PCNSL and GBM. The increased expression level of EGFR in GBM may be achieved by the negative regulatory effects of miR-4433b-5p. The diagnostic performance of the miRNA biomarkers still needs to be further verified in larger sample size cohorts.

Indexed as

Biomarkers, TumorBrain NeoplasmsCentral Nervous System NeoplasmsExosomesGlioblastomaLymphomaMicroRNAsAdultAgedDiagnosis, DifferentialFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleMiddle AgedBiomarkers, TumorMicroRNAsDifferential diagnosisExosomeGlioblastomaMiRNA sequencingPrimary central nervous system lymphoma

Identifiers

PMID41146060
PMCPMC12560364

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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.