Evidence map›Paper›PMID 40547844›Full record

ArticleMolecular therapy. Nucleic acids2025

miRNA-642a-3p protects β cells from glucolipotoxicity.

Sandra Sofia Pinhanços, João Teixeira de Oliveira, C Henrique Alves, Cláudia M Deus, Twan J J de Winter, Sofia Viana, Flávio Reis, Jorge Santos, Mijke Buitinga, Françoise Carlotti and 4 more

Abstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Sandra Sofia PinhançosCNC - Center for Neuroscience and Cell Biology, University of Coimbra, 3060-197 Coimbra, Portugal.
João Teixeira de OliveiraUMIB (Unidade Multidisciplinar de Investigação Biomédica) ICBAS-UP, 4050-346 Porto, Portugal.
C Henrique AlvesClinical Academic Center of Coimbra (CACC), 3004-561 Coimbra, Portugal.
Cláudia M DeusMIA-Portugal, University of Coimbra, 3004-504 Coimbra, Portugal.
Twan J J de WinterDepartment of Internal Medicine, Leiden University Medical Center, 2333 ZA Leiden, the Netherlands.
Sofia VianaClinical Academic Center of Coimbra (CACC), 3004-561 Coimbra, Portugal.
Flávio ReisClinical Academic Center of Coimbra (CACC), 3004-561 Coimbra, Portugal.
Jorge SantosUMIB (Unidade Multidisciplinar de Investigação Biomédica) ICBAS-UP, 4050-346 Porto, Portugal.
Mijke BuitingaNutrition and Movement Sciences, Maastricht University, 6211 LK Maastricht, the Netherlands.
Françoise CarlottiDepartment of Internal Medicine, Leiden University Medical Center, 2333 ZA Leiden, the Netherlands.
Lino FerreiraCNC - Center for Neuroscience and Cell Biology, University of Coimbra, 3060-197 Coimbra, Portugal.
Martin GotthardtDepartment of Medical Imaging, Radboud University Medical Centre, 6525 GA Nijmegen, the Netherlands.
John JonesCNC - Center for Neuroscience and Cell Biology, University of Coimbra, 3060-197 Coimbra, Portugal.
Hugo FernandesCNC - Center for Neuroscience and Cell Biology, University of Coimbra, 3060-197 Coimbra, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The incidence of type 2 diabetes mellitus (T2DM) is tightly linked to obesity. High levels of circulating glucose and saturated free fatty acids (FFAs), known as glucolipotoxicity (GLT), is implicated in β cell dysfunction and/or death. This study aims to identify miRNAs capable of protecting β cells from GLT-induced cell death (GICD). A library of 2,080 human miRNA mimics was transfected in β cells followed by exposure to GLT. We identified 45 miRNAs capable of protecting β cells from GICD and selected miR-642a-3p for further studies. RNA-seq revealed that miR-642a-3p restored the expression of β cell identity genes and modulated pathways associated with cell survival and lipid metabolism. Moreover, we showed that transfection of β cells with miR-642a-3p protected them from GLT-induced changes in insulin secretion. Compared with the control, hypercaloric-fed mice showed a trend toward decreased expression of GLT-protective miRNAs. Notably, we demonstrated that miR-642a-3p expression was downregulated in human islets isolated from T2DM patients compared with non-diabetic controls. Importantly, in obese patients, the expression of GLT-protective miRNAs in plasma-derived extracellular vesicles was increased in non-diabetic patients. Overall, we have identified a potential dual role for miR-642a-3p as both a biomarker and a facilitator of β cell survival and function, offering a novel theranostic tool for the management of diabetes and/or obesity.

Indexed as

bariatric surgerydiabetesextracellular vesiclesglucolipotoxicitymicroRNAsMT: Non-coding RNAsobesityβ cells

Identifiers

PMID40547844
PMCPMC12181781

What Socratic holds

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LicenceCC BY-NC-ND
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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.