ArticleCell reports. Medicine2026
Combined multi-omics and multi-spectral profiling of plasma extracellular vesicles reveals liquid biopsy biomarkers for glioma diagnosis.
Article in Cell reports. Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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.
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.
Who cites it
2 citing papers in PubMed.
- Decoding Glioblastoma Complexity Through Extracellular Vesicles, Organ-on-Chip Models, and Deep Learning.Cells · 2026Review
- Extracellular Vesicles in the Biology and Liquid Biopsy Diagnostics of Pediatric High-Grade Glioma - Emerging Findings and Opportunities.Journal of extracellular biology · 2026Review
Corrections and comments
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Authors and funding
35 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Plasma small extracellular vesicles (sEVs) are a promising liquid biopsy tool. This study aims to delineate and validate a multimodal plasma sEV biomarker signature for glioma. We use size exclusion chromatography to separate sEVs from plasma (1 mL) and a combination of multi-spectral (Fourier transform infrared/Raman) and orthogonal multi-omics (proteomic/microRNA) approaches on 206 plasma samples (159 individuals) across three independent cohorts. We identify distinct glioma sEV biomolecular profiles, including differences in sEV protein/nucleic acid composition, and consistent alterations in 45 proteins and 20 microRNAs. Machine learning models derived from training cohort data achieve high diagnostic performance (areas under the curve [AUCs] 0.931-0.971), while external validation across independent cohorts confirms the signature's diagnostic potential, with 100% accuracy for the proteomic and multimodal signatures in the longitudinal cohort. Our findings, generated through a rigorous multi-cohort and multi-algorithmic framework, establish the potential of plasma sEV signatures as a clinically relevant diagnostic liquid biopsy approach for glioma.
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Registered trials
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 Socratic graph.