Evidence map›Paper›PMID 40788903›Full record

ArticlePloS one2025

Down-regulation of MIR-378A-3P expression associated with inflammation: The effects of restoring its levels.

Marta Seco-Cervera, Laura Gisbert-Ferrándiz, Dulce C Macias-Ceja, Dolores Ortiz-Masiá, Jesús Cosín-Roger, Cristina Bauset, Begoña Heras-Moran, Francisco Navarro-Vicente, Maria Civera-Barrachina, José Santiago Ibáñez-Cabellos and 2 more

Abstract read
In one paragraph

Article in PloS one, 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

12 authors.

Marta Seco-CerveraHospital Universitario Dr. Peset, FISABIO, Valencia, Spain.ORCID https://orcid.org/0000-0002-4278-2835
Laura Gisbert-FerrándizDepartamento de Farmacología, Facultad de Medicina, Universidad de Valencia, Valencia, Spain.
Dulce C Macias-CejaDepartamento de Farmacología, Facultad de Medicina, Universidad de Valencia, Valencia, Spain.
Dolores Ortiz-MasiáDepartamento de Medicina, Facultad de Medicina, Universidad de Valencia, Valencia, Spain.
Jesús Cosín-RogerDepartamento de Farmacología, Facultad de Medicina, Universidad de Valencia, Valencia, Spain.ORCID https://orcid.org/0000-0002-2468-4908
Cristina BausetDepartamento de Farmacología, Facultad de Medicina, Universidad de Valencia, Valencia, Spain.
Begoña Heras-MoranDepartamento de Anatomía Patológica, Facultad de Medicina, Universidad de Valencia, Valencia, Spain.
Francisco Navarro-VicenteHospital de Manises, Valencia, Spain.ORCID https://orcid.org/0000-0002-9775-3169
Maria Civera-BarrachinaDepartamento de Farmacología, Facultad de Medicina, Universidad de Valencia, Valencia, Spain.
José Santiago Ibáñez-CabellosEpiDisease S.L., Scientific Park, University of Valencia, Departamento de Fisiología, Facultad de Medicina, Universidad de Valencia, Valencia, Spain.
Sara CalatayudDepartamento de Farmacología, Facultad de Medicina, Universidad de Valencia, Valencia, Spain.ORCID https://orcid.org/0000-0001-9675-2423
María D BarrachinaDepartamento de Farmacología, Facultad de Medicina, Universidad de Valencia, Valencia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epigenetics has emerged as a modulator of inflammation-related diseases and changes in miRNA expression have been associated with regional location, inflamed mucosa and disease activity in Crohn´s disease (CD). We analyse here the differential ileal miRNA expression in fibrotic tissue from patients with complicated CD and its relevance in inflammation and fibrosis. A miRNA sequencing analysis has been performed in ileal surgical resections from both patients with complicated CD and control subjects. The correlation analysis of data with an mRNA seq study performed in the same samples pointed to hsa-miR-378a-3p as an epigenetic regulator of inflammatory and fibrotic genes. Results demonstrate a significant diminution in the expression of miR-378a-3p in three different inflammatory conditions: ileum from complicated CD patients, intestine from DSS (Dextran Sulfate Sodium)-treated mice and macrophages polarized towards an M1 phenotype. Treatment with miR-378a-3p mimics failed to prevent inflammation and fibrosis in DSS-treated mice while it increased the expression of several cytokines and chemokines in both murine intestine and M1 macrophages. In conclusion, our study shows the downregulation of miR-378a-3p expression in human and murine intestinal inflammation and demonstrates that restoring the intestinal miR-378a-3p levels did not prevent inflammation and fibrosis in murine chronic colitis while intensified the expression of inflammatory and fibrotic markers.

Indexed as

Crohn DiseaseDown-RegulationInflammationMicroRNAsAnimalsColitisDextran SulfateFemaleFibrosisHumansIleumMacrophagesMaleMiceMice, Inbred C57BLDextran SulfateMicroRNAsMIRN378 microRNA, humanMIRN378 microRNA, mouse

Identifiers

PMID40788903
PMCPMC12338774

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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.