Evidence map›Paper›PMID 42050193›Full record

ArticleArchives of toxicology2026

Assessment of cytotoxicity and genomic instability induced by coal-derived nanoparticles in V79 and HaCaT Cells.

Alvaro Miranda-Guevara, Wilner Martínez-López, Grethel León-Mejía, Ornella Fiorillo Moreno, Leonardo Pacheco-Londoño, Julian Rodríguez Tapia, Fredy Jose Torres Cantillo, Maria Fernanda Palma, Paola Hernández, Pablo Liddle and 12 more

Abstract read
In one paragraph

Article in Archives of toxicology, 2026. 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

22 authors.

Alvaro Miranda-GuevaraFacultad de Ciencias Básicas, Centro de Investigaciones en Ciencias de La Vida (CICV), Universidad Simón Bolívar, 080002, Barranquilla, Colombia.
Wilner Martínez-LópezDepartamento de Genética, Instituto de Investigaciones Biológicas Clemente Estable, Ministerio de Educación y Cultura, Montevideo, Uruguay. wilnermartinezlopez@gmail.com.
Grethel León-MejíaFacultad de Ciencias Básicas, Centro de Investigaciones en Ciencias de La Vida (CICV), Universidad Simón Bolívar, 080002, Barranquilla, Colombia. grethel.leon@unisimon.edu.co.ORCID 0000-0002-8326-8592
Ornella Fiorillo MorenoFacultad de Ciencias Básicas, Centro de Investigaciones en Ciencias de La Vida (CICV), Universidad Simón Bolívar, 080002, Barranquilla, Colombia.
Leonardo Pacheco-LondoñoFacultad de Ciencias Básicas, Centro de Investigaciones en Ciencias de La Vida (CICV), Universidad Simón Bolívar, 080002, Barranquilla, Colombia.
Julian Rodríguez TapiaFacultad de Ciencias Básicas, Centro de Investigaciones en Ciencias de La Vida (CICV), Universidad Simón Bolívar, 080002, Barranquilla, Colombia.
Fredy Jose Torres CantilloFacultad de Ciencias Básicas, Centro de Investigaciones en Ciencias de La Vida (CICV), Universidad Simón Bolívar, 080002, Barranquilla, Colombia.
Maria Fernanda PalmaFacultad de Ciencias Básicas, Centro de Investigaciones en Ciencias de La Vida (CICV), Universidad Simón Bolívar, 080002, Barranquilla, Colombia.
Paola HernándezDepartamento de Genética, Instituto de Investigaciones Biológicas Clemente Estable, Ministerio de Educación y Cultura, Montevideo, Uruguay.
Pablo LiddleDepartamento de Genética, Instituto de Investigaciones Biológicas Clemente Estable, Ministerio de Educación y Cultura, Montevideo, Uruguay.
Burix MechosoDepartamento de Genética, Instituto de Investigaciones Biológicas Clemente Estable, Ministerio de Educación y Cultura, Montevideo, Uruguay.
Miriam LópezDepartamento de Genética, Instituto de Investigaciones Biológicas Clemente Estable, Ministerio de Educación y Cultura, Montevideo, Uruguay.
Laura Lafon-HughesDepartamento de Genética, Instituto de Investigaciones Biológicas Clemente Estable, Ministerio de Educación y Cultura, Montevideo, Uruguay.
Lihuén VillarrealLaboratorio de Señalización Celular y Nanobiología, Instituto de Investigaciones Biológicas Clemente Estable, Ministerio de Educación y Cultura, Montevideo, Uruguay.
Juan C BenechLaboratorio de Señalización Celular y Nanobiología, Instituto de Investigaciones Biológicas Clemente Estable, Ministerio de Educación y Cultura, Montevideo, Uruguay.
Renato PugaHospital Israelita Albert Einstein, São Paulo, SP, Brazil.
Jose Eduardo VargasDepartamento de Biologia Celular, Universidade Federal do Paraná, Curitiba, Brazil.
Pedro Fragoso-CastillaGrupo de Investigación Parasitología Agroecología Milenio, Programa de Microbiología - Universidad Popular del Cesar, Valledupar, Colombia.
Milton Quintana-SosaFacultad de Ciencias Básicas, Centro de Investigaciones en Ciencias de La Vida (CICV), Universidad Simón Bolívar, 080002, Barranquilla, Colombia.
Juliana da SilvaPrograma de Pós-Graduação Em Genética E Biologia Molecular (PPGBM), Universidade Federal Do Rio Grande Do Sul (UFRGS), Porto Alegre, RS, Brazil.
João Antonio Pêgas HenriquesPrograma de Pós-Graduação Em Genética E Biologia Molecular (PPGBM), Universidade Federal Do Rio Grande Do Sul (UFRGS), Porto Alegre, RS, Brazil.
Antonio Acosta-HoyosFacultad de Ciencias Básicas, Centro de Investigaciones en Ciencias de La Vida (CICV), Universidad Simón Bolívar, 080002, Barranquilla, Colombia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coal is a major global energy resource, but its extraction raises significant environmental and health concerns. Mining activities release large amounts of particulate matter, including nanoparticles (NPs), into the environment. These NPs are hazardous due to their content of polycyclic aromatic hydrocarbons (PAHs), metals, oxides, and other compounds capable of disrupting cellular and molecular processes. This study evaluated the cytotoxic and genotoxic effects of coal-derived NPs on V79 and HaCaT cell lines, focusing on their impact on DNA stability and the mechanisms responsible for cellular damage. NPs were isolated using an acid-based separation method and applied to cells at concentrations of 50, 150, and 300 μg/mL. Atomic force microscopy (AFM) provided topographical characterization, while dynamic light scattering (DLS) confirmed their tendency to agglomerate. Scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM-EDS) confirmed NP morphology and elemental composition, including carbon, oxygen, iron, calcium, silicon, aluminum, and copper. Cytotoxicity was assessed using resazurin and sulforhodamine B assays, and genotoxicity was evaluated using the comet assay, micronucleus test, and γH2AX immunostaining. Results showed a clear dose-dependent effect, with coal NPs inducing genomic instability and increased cell mortality, mainly through apoptosis. These findings highlight the importance of characterizing coal-derived NPs to better assess their environmental and health risks, particularly regarding respiratory diseases.

Indexed as

CoalGenomic InstabilityNanoparticlesAnimalsCell LineCell SurvivalComet AssayDNA DamageDose-Response Relationship, DrugHaCaT CellsHumansMicronucleus TestsMicroscopy, Atomic ForceParticle SizeCoalCell deathCoal NanoparticlesCytotoxicityGenotoxicityOxidative damage

Identifiers

PMID42050193
PMCPMC13379404

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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.