Evidence map›Paper›PMID 42886463›Full record

ArticleBiometals : an international journal on the role of metal ions in biology, biochemistry, and medicine2026

Toxicogenetic profiling of an antifungal lawsone silver salt: in silico and in vitro analysis in 2D and 3D mammalian models.

Bárbara Verena Dias Galvão, Letícia Mota Candal de Matos, Alana da Cunha Goldstein, Luana P Borba-Santos, Nathália Pinheiro Dos Santos, Caroline Deckmann Nicoletti, Wanderley de Souza, Vitor Francisco Ferreira, Debora Omena Futuro, Sonia Rozental and 2 more

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Article in Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine, 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

12 authors.

Bárbara Verena Dias GalvãoLaboratório de Mutagênese Ambiental, Departamento de Biofísica e Biometria, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0003-3368-5168
Letícia Mota Candal de MatosLaboratório de Mutagênese Ambiental, Departamento de Biofísica e Biometria, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0001-9383-9232
Alana da Cunha GoldsteinLaboratório de Mutagênese Ambiental, Departamento de Biofísica e Biometria, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0003-3261-8799
Luana P Borba-SantosLaboratório de Biologia Celular de Fungos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0001-6576-6646
Nathália Pinheiro Dos SantosLaboratório de Biologia Celular de Fungos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Caroline Deckmann NicolettiDepartamento de Tecnologia Farmacêutica, Faculdade de Farmácia, Universidade Federal Fluminense, Niteroi, RJ, Brazil.ORCID http://orcid.org/0000-0003-4357-1092
Wanderley de SouzaLaboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0002-1895-1299
Vitor Francisco FerreiraDepartamento de Tecnologia Farmacêutica, Faculdade de Farmácia, Universidade Federal Fluminense, Niteroi, RJ, Brazil.ORCID http://orcid.org/0000-0002-2166-766X
Debora Omena FuturoDepartamento de Tecnologia Farmacêutica, Faculdade de Farmácia, Universidade Federal Fluminense, Niteroi, RJ, Brazil.ORCID http://orcid.org/0000-0002-9152-4330
Sonia RozentalLaboratório de Biologia Celular de Fungos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0002-3659-5945
Carlos Fernando Araujo-LimaLaboratório de Mutagênese Ambiental, Departamento de Biofísica e Biometria, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil. araujo.lima@unirio.br.ORCID http://orcid.org/0000-0002-9278-4441
Israel FelzenszwalbLaboratório de Mutagênese Ambiental, Departamento de Biofísica e Biometria, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0003-1677-197X

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 303994/2025-8Coordination for Superior Level Staff Improvement (CAPES) Code 0001Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/010.002119/2019Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/200.510/2025Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E- 26/202.759/2017Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro, Brazil E-26/200839/2021National Council for Scientific and Technological Development (CNPq) 140113/2022-3National Council for Scientific and Technological Development (CNPq) 305600/2021-4National Council for Scientific and Technological Development (CNPq) 408259/2023-0
6 · The paper itself

Abstract

The development of novel metal-based antifungals requires rigorous characterization of their toxicological mechanisms to ensure patient safety. This study investigated the toxicogenetic profile and cellular interactions of lawsone silver salt (LSS), a compound with established activity against Sporothrix spp. and emerging multidrug-resistant pathogens. Antifungal efficacy was confirmed against planktonic Aspergillus fumigatus, Candida albicans, and C. auris (MIC 1.45-23.2 µM), with significant anti-biofilm activity against C. albicans (185.9 µM) and A. fumigatus (92.9 µM). In silico ADMET modeling predicted high oral bioavailability and blood-brain barrier permeability, despite the genotoxicity alerts. Experimentally, LSS (0.005-50 µg/plate) was non-mutagenic in the Salmonella/microsome assay (TA1535, TA97a, TA98, TA100, and TA102), regardless of the metabolic activation. However, LSS (0.5-500 µM) induced significant genomic instability in HepG2 cells. The micronucleus assay revealed a dose-dependent increase in micronuclei, nucleoplasmic bridges, and nuclear buds, indicating clastogenic and aneugenic effects. Comparative cytotoxicity was evaluated in BALB/3T3 fibroblasts using 2D monolayers and scaffold-based 3D models (0.005-5000 µM). In 2D cultures, LSS exhibited potent cytotoxicity (CC

Indexed as

Alternative methodsAntifungal activityCytotoxicityGenotoxicityMutagenicityNaphthoquinones

Identifiers

PMID42886463

What OpenQuestion holds

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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.