Evidence map›Paper›PMID 41028098›Full record

ArticleScientific reports2025

GLRX2 polymorphism and oxidative stress levels impact urothelial bladder cancer outcomes.

Isabely M Silva, Beatriz G L Vacario, Flora T Maraslis, Alexsandro Koike, Maria E P Simonato, Carolina Coradi, Alvaro J Fernandes, Andréa N C Simão, Marcell A B Lozovoy, Gustavo R M Barcelos and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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

14 authors.

Isabely M Silva *Laboratory of Mutagenesis and Oncogenetics, Department of General Biology, Center of Biological Sciences, State University of Londrina (UEL), Rodovia Celso Garcia Cid - PR 445 Km 380 Cx. Postal 10.011 - Campus Universitário, Londrina, PR, 86057-970, Brazil.
Beatriz G L Vacario *Laboratory of Mutagenesis and Oncogenetics, Department of General Biology, Center of Biological Sciences, State University of Londrina (UEL), Rodovia Celso Garcia Cid - PR 445 Km 380 Cx. Postal 10.011 - Campus Universitário, Londrina, PR, 86057-970, Brazil.
Flora T MaraslisDepartment of Biosciences, Institute for Health and Society, Federal University of São Paulo (UNIFESP), Santos, 11060-001, Brazil.
Alexsandro KoikeLondrina Cancer Hospital, Londrina, 86015-520, Brazil.
Maria E P SimonatoLaboratory of Tumor Biology, Health Sciences Center, State University of West Paraná (UNIOESTE), Francisco Beltrão, PR, 85605-010, Brazil.
Carolina CoradiLaboratory of Tumor Biology, Health Sciences Center, State University of West Paraná (UNIOESTE), Francisco Beltrão, PR, 85605-010, Brazil.
Alvaro J FernandesLaboratory of Research in Applied Immunology, Department of Pathology, Clinical Analysis and Toxicology, Health Sciences Center, University of Londrina, Londrina, Paraná, 86038-440, Brazil.
Andréa N C SimãoLaboratory of Research in Applied Immunology, Department of Pathology, Clinical Analysis and Toxicology, Health Sciences Center, University of Londrina, Londrina, Paraná, 86038-440, Brazil.
Marcell A B LozovoyLaboratory of Research in Applied Immunology, Department of Pathology, Clinical Analysis and Toxicology, Health Sciences Center, University of Londrina, Londrina, Paraná, 86038-440, Brazil.
Gustavo R M BarcelosDepartment of Biosciences, Institute for Health and Society, Federal University of São Paulo (UNIFESP), Santos, 11060-001, Brazil.
Mateus L FalcoDepartment of Pharmaceutical Sciences, Midwestern State University (Unicentro), Guarapuava, Paraná, 85015-430, Brazil.
Roberta Losi GuembarovskiLaboratory of Mutagenesis and Oncogenetics, Department of General Biology, Center of Biological Sciences, State University of Londrina (UEL), Rodovia Celso Garcia Cid - PR 445 Km 380 Cx. Postal 10.011 - Campus Universitário, Londrina, PR, 86057-970, Brazil.
Carolina PanisLaboratory of Tumor Biology, Health Sciences Center, State University of West Paraná (UNIOESTE), Francisco Beltrão, PR, 85605-010, Brazil.
Juliana Mara SerpeloniLaboratory of Mutagenesis and Oncogenetics, Department of General Biology, Center of Biological Sciences, State University of Londrina (UEL), Rodovia Celso Garcia Cid - PR 445 Km 380 Cx. Postal 10.011 - Campus Universitário, Londrina, PR, 86057-970, Brazil. julianaserpeloni@uel.br.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 404610/2021-8Conselho Nacional de Desenvolvimento Científico e Tecnológico , Brasil 30335/2021-9Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 01
6 · The paper itself

Abstract

The bladder is continuously exposed to oxidative and mutagenic agents. Such chemicals are metabolized, filtered by the kidneys, and excreted in the urine. Not surprisingly, urothelial bladder cancer (UBC) is the 9th most common cancer worldwide. This study investigates whether the C > T (rs912071) polymorphism in the Glutaredoxin 2 (GLRX2) gene, oxidative stress marker levels, and GLRX2 expression are associated with prognosis and recurrence in 341 patients with UBC. Gene expression data were compared to those available in TCGA. The TT genotype (OR = 2.475, p = 0.017) was positively associated with the risk of 1-year recurrence. Hypertensive patients carrying the CT genotype presented a reduced risk for recurrence (OR = 0.460, p = 0.047) and high-grade tumors (OR = 0.188, p = 0.001). Lipid peroxidation and nitric oxide metabolites (NOx) levels were higher in patients than in controls and in patients carrying the TT genotype. Tumor tissues and invasive tumors had higher GLRX2 expression, confirming the TCGA findings. DepMap analysis identifies GLRX2 as a valuable tool enabling personalized treatments for UBC patients. Our results showed that the TT genotype of rs912071 is associated with an increased risk of recurrence and high oxidative stress. In contrast, the CT genotype may protect against disease recurrence in patients with UBC cancer.

Indexed as

Oxidative StressPolymorphism, Single NucleotideUrinary Bladder NeoplasmsAgedFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedNeoplasm Recurrence, LocalNitric OxidePrognosisNitric OxideGRX2Oxidative stressRecurrenceUrothelial bladder cancer

Identifiers

PMID41028098
PMCPMC12484609

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LicenceCC BY-NC-ND
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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.