Evidence map›Paper›PMID 40332030›Full record

ArticleInternational journal of molecular sciences2025

Extracellular Competing Endogenous RNA Networks Reveal Key Regulators of Early Amyloid Pathology Propagation in Alzheimer's Disease.

Misael Leonardo López-Cepeda, Andrea Angarita-Rodríguez, Alexis Felipe Rojas-Cruz, Julián Pérez Mejia, Robin Khatri, Michael Brehler, Eduardo Martínez-Martínez, Andrés Pinzón, Andrés Felipe Aristizabal-Pachon, Janneth González

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.

Misael Leonardo López-CepedaDepartamento de Nutrición y Bioquímica, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.ORCID 0000-0003-2676-2292
Andrea Angarita-RodríguezDepartamento de Nutrición y Bioquímica, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.
Alexis Felipe Rojas-CruzDepartamento de Nutrición y Bioquímica, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.ORCID 0000-0003-4467-0914
Julián Pérez MejiaDepartamento de Nutrición y Bioquímica, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.ORCID 0009-0000-8164-0330
Robin KhatriInstitute of Medical Systems Bioinformatics, University Medical Center Hamburg-Eppendorf, 20251 Hamburg, Germany.
Michael BrehlerInstitute of Medical Systems Bioinformatics, University Medical Center Hamburg-Eppendorf, 20251 Hamburg, Germany.
Eduardo Martínez-MartínezLaboratory of Cell Communication & Extracellular Vesicles, Instituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.ORCID 0000-0002-9020-559X
Andrés PinzónLaboratorio de Bioinformática y Biología de Sistemas, Universidad Nacional de Colombia, Bogotá 111321, Colombia.
Andrés Felipe Aristizabal-PachonDepartamento de Nutrición y Bioquímica, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.ORCID 0000-0003-3004-4867
Janneth GonzálezDepartamento de Nutrición y Bioquímica, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.ORCID 0000-0003-2009-3374

Funding

Minciencias 94314, contract 014-2023Pontificia Universidad Javeriana 20644
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are small capsular bodies released by cells, mediating responses in intercellular communication. The role of EVs in Aβ pathology spreading in the Alzheimer's disease (AD) brain has been evidenced, although whether this occurs due to the co-transportation of Aβ peptides or contribution of other factors, such as EV-associated transcripts, remains uncertain. In vitro studies of miRNA cargo in neuron-derived extracellular vesicles (NDEVs) show that Aβ hyperexpression alters the transcriptomic profile; however, it is not clear to what extent this causes changes at the organ level. By utilizing datasets from published studies, we generated competing endogenous RNA (ceRNA) networks for miRNAs co-expressed in NDEVs and the brain in different stages of pathology, using both an APP overexpressing neuronal model (in vitro) and brain cortices from 6- and 9-month-old APP/PSEN1 mice (in vivo). Networks integrating information from mRNAs, lncRNAs, and circRNAs showed two candidate lncRNAs (Kcnq1ot1 and Gm42969) and a circRNA (Pum1), while enrichment analyses detected that NDEVs miRNAs signal to other CNS cells and that this signal can be disrupted by Aβ pathology, contributing to the loss of long-term potentiation seen in early AD.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesExtracellular VesiclesGene Regulatory NetworksAmyloid beta-Protein PrecursorAnimalsBrainDisease Models, AnimalHumansMiceMice, TransgenicMicroRNAsNeuronsRNA, CircularRNA, Competitive EndogenousRNA, Long NoncodingAmyloid beta-PeptidesAmyloid beta-Protein PrecursorMicroRNAsRNA, CircularRNA, Competitive EndogenousRNA, Long NoncodingRNA, Messengeramyloidogenic pathwayAβ pathologycompetitive endogenous RNA network (ceNET)exosomemiRNA

Identifiers

PMID40332030
PMCPMC12027385

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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.