Evidence map›Paper›PMID 40640506›Full record

ArticleScientific reports2025

Human umbilical vein endothelial cell miRNA secretome highlights endothelial origin of serum miRNAs.

Nora J Doleschall, Zoltán F Doleschall, Flóra Demeter, Márta L Debreczeni, Erika Kajdácsi, László Cervenak, Katalin Keltai

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

7 authors.

Nora J DoleschallInstitute of Genetics and Cancer, The University of Edinburgh, Western General Hospital Campus, Crewe Road, Edinburgh, EH4 2XU, UK.
Zoltán F DoleschallResearch Laboratory, Department of Internal Medicine and Haematology, Semmelweis University, Szentkirályi u. 46, Budapest, 1088, Hungary.
Flóra DemeterResearch Laboratory, Department of Internal Medicine and Haematology, Semmelweis University, Szentkirályi u. 46, Budapest, 1088, Hungary.
Márta L DebreczeniResearch Laboratory, Department of Internal Medicine and Haematology, Semmelweis University, Szentkirályi u. 46, Budapest, 1088, Hungary.
Erika KajdácsiResearch Laboratory, Department of Internal Medicine and Haematology, Semmelweis University, Szentkirályi u. 46, Budapest, 1088, Hungary.
László CervenakResearch Laboratory, Department of Internal Medicine and Haematology, Semmelweis University, Szentkirályi u. 46, Budapest, 1088, Hungary. cervenak.laszlo@semmelweis.hu.
Katalin KeltaiResearch Laboratory, Department of Internal Medicine and Haematology, Semmelweis University, Szentkirályi u. 46, Budapest, 1088, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs are key contributors to blood-based biomarker research, however their potential is hindered by the "noise" of their abundance even in healthy blood. Using HUVEC cultures and their conditioned media as a model for endothelium and blood, we were able to detect 574 different microRNAs. 166 of these were exclusively secreted, 155 only intracellular and 253 were found in both states suggesting a highly ordered role in endocrine and paracrine communication. The identified microRNA signatures exhibited higher degrees of variability based on culture conditions rather than genetic background of donors. We found that the endothelial secreted microRNA signature correlates greatly with those found in blood serum (ρ = 0.749 ± 0.044), more so, than leukocyte secretory microRNAs (ρ = 0.531 ± 0.044). These results demonstrate that the endothelium actively secretes microRNAs dominating the microRNA composition of the blood making the endothelial secretory microRNA signatures ideal representation of background "noise" of healthy serum samples. These microRNA signatures are readily adapted to environmental cues; making the standardisation of culture conditions a key concern. Our results also demonstrate that the microarray technology has great use in precision microRNA biomarker discovery using simple models, which should be utilised for further mapping of cell-type specific healthy signatures to further refine blood-based diagnostics.

Indexed as

Human Umbilical Vein Endothelial CellsMicroRNAsSecretomeBiomarkersCells, CulturedCulture Media, ConditionedGene Expression ProfilingHumansBiomarkersCulture Media, ConditionedMicroRNAs

Identifiers

PMID40640506
PMCPMC12246433

What Socratic holds

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LicenceCC BY
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Registered trials

None linked

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.