Evidence mapPaperPMID 41644049Full record

ArticleMolecular & cellular proteomics : MCP2026

Distinct Proteomic and Glycosylation Signatures Differentiate A549 Tumor and BEAS-2B Nontumor Cell Line-Derived Small Extracellular Vesicles.

Mirjam Balbisi, Tamás Langó, Virág Nikolett Horváth, Domonkos Pál, Gitta Schlosser, Gábor Kecskeméti, Zoltán Szabó, Kinga Ilyés, Nikolett Nagy, Otília Tóth and 6 more

Abstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2026. 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
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

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. Review
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

16 authors.

Mirjam BalbisiMTA-HUN-REN TTK Lendület (Momentum) Glycan Biomarker Research Group, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary; Doctoral School, Semmelweis University, Budapest, Hungary.
Tamás LangóInstitute of Molecular Life Sciences, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.
Virág Nikolett HorváthMTA-HUN-REN TTK Lendület (Momentum) Glycan Biomarker Research Group, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.
Domonkos PálMTA-HUN-REN TTK Lendület (Momentum) Glycan Biomarker Research Group, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary; Doctoral School, Semmelweis University, Budapest, Hungary.
Gitta SchlosserMTA-ELTE Lendület (Momentum) Ion Mobility Mass Spectrometry Research Group, ELTE Eötvös Loránd University, Institute of Chemistry, Budapest, Hungary.
Gábor KecskemétiDepartment of Medical Chemistry, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Zoltán SzabóDepartment of Medical Chemistry, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Kinga IlyésBiological Nanochemistry Research Group, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary; Hevesy György PhD School of Chemistry, ELTE Eötvös Loránd University, Budapest, Hungary.
Nikolett NagyInstitute of Molecular Life Sciences, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.
Otília TóthInstitute of Molecular Life Sciences, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary; Department of Applied Biotechnology and Food Science, Faculty of Chemical Technology and Biotechnology, BME Budapest University of Technology and Economics, Budapest, Hungary.
Jing ZhengAnalytical Biochemistry, Groningen Research Institute of Pharmacy, University of Groningen, Groningen, The Netherlands.
Guinevere S M Lageveen-KammeijerAnalytical Biochemistry, Groningen Research Institute of Pharmacy, University of Groningen, Groningen, The Netherlands.
Tamás VisnovitzDepartment of Genetics, Cell and Immunobiology, Semmelweis University, Budapest, Hungary; Department of Plant Physiology and Molecular Plant Biology, ELTE Eötvös Loránd University, Budapest, Hungary.
Zoltán VargaBiological Nanochemistry Research Group, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary; Department of Physical Chemistry and Materials Science, BME Budapest University of Technology and Economics, Budapest, Hungary.
Beáta G VértessyInstitute of Molecular Life Sciences, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary; Department of Applied Biotechnology and Food Science, Faculty of Chemical Technology and Biotechnology, BME Budapest University of Technology and Economics, Budapest, Hungary.
Lilla TuriákMTA-HUN-REN TTK Lendület (Momentum) Glycan Biomarker Research Group, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary; Doctoral School, Semmelweis University, Budapest, Hungary. Electronic address: turiak.lilla@ttk.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicles (EVs) are central to intercellular communication and have gained attention as rich sources of molecular information in cancer research, but their molecular composition remains incompletely characterized. Protein glycosylation is a frequent post-translational modification; however, most EV studies focus on proteomics, whereas mapping glycosylation changes of proteins is still under-represented. To address this gap, we analyzed the proteomic, N-glycoproteomic, and chondroitin sulfate/dermatan sulfate (CS/DS) glycosaminoglycan (GAG) profiles of small EVs (sEVs) derived from A549 lung adenocarcinoma and BEAS-2B nontumorigenic epithelial cells. Principal component analysis and hierarchical clustering revealed that all three profiles strongly reflect sEV origin. Comparative proteomic analysis showed enrichment of proteins associated with cell cycle regulation, DNA repair, metabolism, and protein synthesis in A549 sEVs, whereas immune-related processes were enriched in BEAS-2B sEVs. Five differentially expressed CS proteoglycans were identified, highlighting the value of complementary GAG-level analysis. N-glycoproteomics revealed a shift from oligomannose to complex N-glycans in A549 sEVs. Prominent glycoproteins with multiple glycosylation sites included versican, galectin-3-binding protein, and laminins. CS/DS content increased 3.4-fold in A549 sEVs, whereas the ratio of the two monosulfated disaccharides changed twofold. These findings demonstrate the utility of N-glycoproteomics and GAG profiling for sensitively characterizing molecular differences between sEVs derived from different cell culture models, thereby providing a foundation for future EV biomarker studies.

Indexed as

Extracellular VesiclesLung NeoplasmsProteomeProteomicsA549 CellsCell LineCell Line, TumorChondroitin SulfatesDermatan SulfateEpithelial CellsGlycoproteinsGlycosylationHumansChondroitin SulfatesDermatan SulfateGlycoproteinsProteomechondroitin/dermatan sulfateextracellular vesiclemass spectrometryN-glycoproteomicsproteomics

Identifiers

PMID41644049
PMCPMC12992954

What Socratic 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 Socratic graph.