Evidence map›Paper›PMID 41171011›Full record

ArticleAging cell2025

miR-140-5p Overexpression Contributes to Oxidative Stress and Mitochondrial Dysfunction in Hutchinson-Gilford Progeria Syndrome Fibroblasts Through NRF2 Pathway.

Léa Toury, Diane Frankel, Sara Nael, Mario Abaji, Léa Le Goff, Marie Basset, Coraline Airault, Bertrand Vernay, Elva María Novoa-Del-Toro, Catherine Bartoli and 4 more

Abstract read
In one paragraph

Article in Aging cell, 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

14 authors.

Léa TouryAix Marseille Université, INSERM, MMG, Marseille, France.ORCID 0000-0003-2148-9768
Diane FrankelAix Marseille Université, APHM, INSERM, MMG, Service de Biologie Cellulaire, Hôpital la Timone, Marseille, France.ORCID 0000-0003-3321-6951
Sara NaelAix Marseille Université, INSERM, MMG, Marseille, France.
Mario AbajiAix Marseille Université, APHM, INSERM, MMG, M2GM, Hôpital la Timone, Marseille, France.ORCID 0000-0003-1562-2024
Léa Le GoffAix Marseille Université, INSERM, MMG, Marseille, France.
Marie BassetAix Marseille Université, INSERM, MMG, Marseille, France.
Coraline AiraultAix Marseille Université, INSERM, MMG, Marseille, France.ORCID 0000-0001-6526-0135
Bertrand VernayAix Marseille Université, CNRS, INP UMR7051, Neuro-Cellular Imaging Service and Nikon Center for Neuro-NanoImaging, Marseille, France.ORCID 0000-0002-7843-3872
Elva María Novoa-Del-ToroAix Marseille Université, INSERM, MMG, Marseille, France.ORCID 0000-0002-6135-5839
Catherine BartoliAix Marseille Université, INSERM, MMG, Marseille, France.
Anaïs BaudotAix Marseille Université, INSERM, MMG, Marseille, France.ORCID 0000-0003-0885-7933
Frederique MagdinierAix Marseille Université, INSERM, MMG, Marseille, France.ORCID 0000-0002-0159-9559
Elise KaspiAix Marseille Université, APHM, INSERM, MMG, Service de Biologie Cellulaire, Hôpital la Timone, Marseille, France.ORCID 0000-0003-0458-5109
Patrice RollAix Marseille Université, APHM, INSERM, MMG, Service de Biologie Cellulaire, Hôpital la Timone, Marseille, France.ORCID 0000-0002-0045-5641

Funding

AFM-Téléthon MoThARD 2021-2025AFM-Téléthon TRIM-RD 2016-2020Institut National de la Santé et de la Recherche Médicale (INSERM)Marseille Maladies Rares (MarMaRa) InstituteMinistère de l'Enseignement Supérieur et de la Recherche (France)
6 · The paper itself

Abstract

Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare, fatal genetic disorder characterized by accelerated aging. The accumulation of an abnormal and toxic protein called progerin within HGPS nuclei disrupts cellular processes, including gene expression and DNA repair. Oxidative stress, resulting from an imbalance between reactive oxygen species (ROS) production and antioxidant defense, is one of the hallmarks of HGPS. To identify novel molecular mechanisms underlying HGPS pathogenesis, we performed miRNA expression profiling in HGPS compared to healthy control fibroblasts. We identified 10 differentially expressed (DE) miRNAs between HGPS and control cells. We focused on miR-140-5p and miR-140-3p, 2 miRNAs upregulated in HGPS fibroblasts. miR-140-5p is known to directly target the transcript of NRF2, a master regulator of the antioxidant response. Using in vitro mimic and antimiR transfections, we demonstrated that miR-140-5p overexpression in HGPS fibroblasts results in the downregulation of the NRF2/KEAP1/HO-1 antioxidant pathway, leading to increased oxidative stress. Furthermore, our results indicate that miR-140-5p overexpression induces mitochondrial dysfunction, characterized by a reduced oxidative phosphorylation capacity and affects other hallmarks of aging. By targeting regulation of oxidative stress and mitochondrial function through NRF2, miR-140-5p may play a pivotal role in the pathophysiology of HGPS and open new therapeutic avenues.

Indexed as

FibroblastsMicroRNAsMitochondriaNF-E2-Related Factor 2Oxidative StressProgeriaHumansReactive Oxygen SpeciesSignal TransductionMicroRNAsMirn140 microRNA, humanNFE2L2 protein, humanNF-E2-Related Factor 2Reactive Oxygen SpeciesHutchinson‐Gilford progeria syndromelaminsmicroRNAmiR‐140mitochondriaNRF2oxidative stress

Identifiers

PMID41171011
PMCPMC12686586

What OpenQuestion 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 OpenQuestion graph.