Evidence map›Paper›PMID 40076764›Full record

ArticleInternational journal of molecular sciences2025

Characterization of the Temporal Dynamics of the Endothelial-Mesenchymal-like Transition Induced by Soluble Factors from Dengue Virus Infection in Microvascular Endothelial Cells.

Jenny Paola Alfaro-García, Carlos Alberto Orozco-Castaño, Julián Andrés Sánchez-Rendón, Herley Fernando Casanova-Yépes, Miguel Vicente-Manzanares, Juan Carlos Gallego-Gómez

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. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Role of c-ABL in DENV-2 Infection and Actin Remodeling in Vero Cells.International journal of molecular sciences · 2025
    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

6 authors.

Jenny Paola Alfaro-GarcíaGrupo Medicina de Translación-Facultad de Medicina, Universidad de Antioquia, Medellín 050010, Colombia.ORCID 0000-0002-7274-4469
Carlos Alberto Orozco-CastañoGrupo de Biología del Cáncer, Instituto Nacional de Cancerología, Bogotá 111511, Colombia.
Julián Andrés Sánchez-RendónGrupo de Coloides-Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia, Medellín 050010, Colombia.ORCID 0009-0000-4909-988X
Herley Fernando Casanova-YépesGrupo de Coloides-Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia, Medellín 050010, Colombia.
Miguel Vicente-ManzanaresMolecular Mechanisms Program, Centro de Investigación del Cáncer, Instituto de Biología Molecular y Celular del Cáncer, Consejo Superior de Investigaciones Científicas (CSIC)-University of Salamanca, 37007 Salamanca, Spain.ORCID 0000-0001-5943-3220
Juan Carlos Gallego-GómezGrupo Medicina de Translación-Facultad de Medicina, Universidad de Antioquia, Medellín 050010, Colombia.ORCID 0000-0001-7453-2569

Funding

Sci. Min. (Colombia) grant CTO 917-2019Universidad de Antioquia grant CODI-2020-34137 (JCG-G)Universidad de Antioquia grant PID2020-116232RB-I00
6 · The paper itself

Abstract

Dengue virus (DV) infection poses a severe life-threatening risk in certain cases. This is mainly due to endothelial dysregulation, which causes plasma leakage and hemorrhage. However, the etiology of DV-induced endothelial dysregulation remains incompletely understood. To identify the potential mechanisms of endothelial dysregulation caused by DV, the effects of conditioned media from Dengue virus (CMDV) on the mechanics and transcriptional profile of the endothelial cells were examined using permeability assays, atomic force microscopy, In-Cell Western blot and in silico transcriptomics. Exposure of HMEC-1 cells to the CMDV increased endothelial permeability and cellular stiffness. It also induced the expression of the key proteins associated with endothelial-to-mesenchymal transition (EndMT). These data support the notion that the DV promotes endothelial dysfunction by triggering transcriptional programs that compromise the endothelial barrier function. Understanding the molecular mechanisms underlying DV-induced endothelial dysregulation is crucial for developing targeted therapeutic strategies to mitigate the severe outcomes associated with dengue infection.

Indexed as

DengueDengue VirusEndothelial CellsEpithelial-Mesenchymal TransitionCell LineCulture Media, ConditionedHumansCulture Media, Conditionedconditioned culture mediumdengue virusendothelial permeabilityplasticitytrans-differentiation

Identifiers

PMID40076764
PMCPMC11900998

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.