Evidence map›Paper›PMID 40362382›Full record

ArticleInternational journal of molecular sciences2025

Identification of eccDNA in Extracellular Vesicles Derived from Human Dermal Fibroblasts Through Nanopore Sequencing.

Bianca Simonassi-Paiva, Julia Alves Luz, Julia Hellena Ribeiro, Juliano Coelho da Silveira, Camila Azzolin de Souza, Georgios Joannis Pappas, Juliana Lott de Carvalho, Mark Lynch, Robert Pogue, Neil J Rowan

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

10 authors.

Bianca Simonassi-PaivaFaculty of Science & Health, Technological University of the Shannon, Athlone Campus, N37HD68 Athlone, Ireland.ORCID 0000-0002-8486-1275
Julia Alves LuzDepartment of Cell Biology, University of Brasilia, Brasilia 70910-900, DF, Brazil.
Julia Hellena RibeiroGenomic Sciences and Biotechnology Program, Catholic University of Brasília, Brasilia 71966-700, DF, Brazil.
Juliano Coelho da SilveiraDepartment of Veterinary Medicine, School of Animal Sciences and Food Engineering, University of São Paulo, Pirassununga 13635-900, SP, Brazil.
Camila Azzolin de SouzaDepartment of Veterinary Medicine, School of Animal Sciences and Food Engineering, University of São Paulo, Pirassununga 13635-900, SP, Brazil.
Georgios Joannis PappasDepartment of Cell Biology, University of Brasilia, Brasilia 70910-900, DF, Brazil.ORCID 0000-0002-1100-976X
Juliana Lott de CarvalhoFaculty of Medicine, University of Brasilia, Brasilia 70910-900, DF, Brazil.ORCID 0000-0002-1423-0523
Mark LynchFaculty of Science & Health, Technological University of the Shannon, Athlone Campus, N37HD68 Athlone, Ireland.
Robert PogueGenomic Sciences and Biotechnology Program, Catholic University of Brasília, Brasilia 71966-700, DF, Brazil.
Neil J RowanFaculty of Science & Health, Technological University of the Shannon, Athlone Campus, N37HD68 Athlone, Ireland.ORCID 0000-0003-1228-3733

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extrachromosomal circular DNAs (eccDNAs) are heterogeneous circular DNA molecules derived from genomic DNA, and believed to be involved in intercellular communication and in natural biological processes. Extracellular vesicles (EVs) are membrane-bound particles released from all cells, and have been shown to contain various classes of nucleic acids. EVs can play a role in intercellular communication and may be used as biomarkers. This constitutes the first study to demonstrate that EVs derived from healthy human dermal fibroblasts carry eccDNA. eccDNA from EVs and their corresponding donor cells were isolated and sequenced on the Oxford Nanopore MinIon platform, followed by the identification of potential eccDNAs through four different bioinformatic pipelines, namely ecc_Finder, cyrcular-calling, CReSIL, and Flec. Our main findings demonstrate that EVs derived from human dermal fibroblasts carry eccDNA; there is variability in the number of eccDNAs identified in the same sample through different pipelines; and there is variability in the identified eccDNAs across biological replicates. Additionally, eccDNAs characterized in this research had (a) sequences as small as 306 base pairs and as large as 28,958 base pairs across all samples, (b) uneven chromosomal distribution, and (c) an average of 49.7% of the identified eccDNAs harboring gene fragments. Future implications for this novel research include using this framework method to elucidate factors and conditions that may influence the skin aging process and related biogenesis in human dermal cells.

Indexed as

DNA, CircularExtracellular VesiclesFibroblastsNanopore SequencingComputational BiologyDermisHumansSkinDNA, Circularbioinformatic pipelineseccDNAEVextracellular vesicleshuman dermal fibroblastslong-read sequencingnanopore sequencing

Identifiers

PMID40362382
PMCPMC12071958

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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.