Evidence map›Paper›PMID 37076894›Full record

ArticleStem cell research & therapy2023

Targeting G-quadruplex motifs interferes with differentiation of adipose-derived mesenchymal stem cells.

Maria Rosaria Ambrosio, Teresa Migliaccio, Fabiana Napolitano, Sarah Di Somma, Giovanni Maneli, Jussara Amato, Bruno Pagano, Antonio Randazzo, Giuseppe Portella, Pietro Formisano and 1 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2023. 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
0.5field-weighted citation impact, top 34% of its field
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, 3 citations in OpenAlex.

  1. Review
  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

11 authors at 2 institutions in 1 country.

Maria Rosaria AmbrosioDepartment of Translational Medical Sciences, University "Federico II", 80131, Naples, Italy.
Teresa MigliaccioDepartment of Translational Medical Sciences, University "Federico II", 80131, Naples, Italy.
Fabiana NapolitanoDepartment of Translational Medical Sciences, University "Federico II", 80131, Naples, Italy.
Sarah Di SommaDepartment of Translational Medical Sciences, University "Federico II", 80131, Naples, Italy.
Giovanni ManeliDepartment of Translational Medical Sciences, University "Federico II", 80131, Naples, Italy.
Jussara AmatoDepartment of Pharmacy, University of Naples Federico II, 80131, Naples, Italy.
Bruno PaganoDepartment of Pharmacy, University of Naples Federico II, 80131, Naples, Italy.
Antonio RandazzoDepartment of Pharmacy, University of Naples Federico II, 80131, Naples, Italy.
Giuseppe PortellaDepartment of Translational Medical Sciences, University "Federico II", 80131, Naples, Italy.
Pietro FormisanoDepartment of Translational Medical Sciences, University "Federico II", 80131, Naples, Italy. fpietro@unina.it.
Anna Maria MalfitanoDepartment of Translational Medical Sciences, University "Federico II", 80131, Naples, Italy. annamaria.malfitano@unina.it.ORCID 0000-0002-6193-2835
Federico II University Hospital · ITUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundG-quadruplex (G4) motifs are nucleic acid secondary structures observed in mammalian genomes and transcriptomes able to regulate various cellular processes. Several small molecules have been developed so far to modulate G4 stability, frequently associated with anticancer activity. However, how G4 structures are regulated over homeostatic conditions is mostly unexplored. Here, we used human adipose-derived mesenchymal stem cells (ASCs) to address the role of G4 motifs during adipogenic differentiation.

methodsAdipocyte differentiation of ASCs was investigated in the presence or absence of a well-known G4 ligand, Braco-19. Cell viability was determined by sulforhodamine B assay. Cell dimension and granularity, DNA G4 motifs and cell cycle were detected by flow cytometry. Lipid droplet accumulation was assessed by Oil Red O staining. Cell senescence was evaluated by β-galactosidase staining. Gene expression was measured by qPCR. Protein release in the extracellular medium was quantified by ELISA.

resultsBraco-19 used at non-cytotoxic concentrations induced morphological changes in mature adipocytes partially restoring an undifferentiated-like status. Braco-19 reduced lipid vacuolization and PPARG, AP2, LEP and TNFA mRNA levels in terminally differentiated cells. No effect was observed in cell senescence, fibrotic markers, IL-6 and IL-8 production, while the secretion of VEGF was dose-dependently reduced. Interestingly, G4 structures were increased in differentiated adipocytes compared to their precursors. Braco-19 treatment reduced G4 content in mature adipocytes.

conclusionsOur data highlight a new role of G4 motifs as genomic structural elements related to human ASC differentiation into mature adipocytes, with potential implications in physio-pathological processes.

Indexed as

AdipocytesMesenchymal Stem CellsAdipogenesisAnimalsCell DifferentiationCells, CulturedHumansMammalsProteinsProteinsAdipocytesDifferentiationG-quadruplexMesenchymal stem cells

Identifiers

PMID37076894
PMCPMC10116735
OpenAlexW4366580369

What Socratic holds

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LicenceCC BY
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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 Socratic graph.