Evidence map›Paper›PMID 42353062›Full record

ArticleInternational journal of molecular sciences2026

Integrated Assessment of HIF-1α and SOD2 Expression and Their Prognostic Implications in Triple-Negative Breast Cancer.

Burcu Sanal Yılmaz, Sezer Seda Yılmaz, Zeliha Esin Çelik

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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5 · Who and what money

Authors and funding

3 authors.

Burcu Sanal YılmazDepartment of Pathology, Faculty of Medicine, Karamanoğlu Mehmetbey University, Karaman 70200, Turkey.
Sezer Seda YılmazVan Branch of the Council of Forensic Medicine, Van 65080, Turkey.
Zeliha Esin ÇelikDepartment of Pathology, Faculty of Medicine, Selcuk University, Konya 42130, Turkey.ORCID 0000-0002-3220-7845

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is characterized by aggressive clinical behavior and limited targeted therapeutic options. Hypoxia signaling mediated by hypoxia-inducible factor-1α (HIF-1α) and mitochondrial antioxidant defense driven by superoxide dismutase 2 (SOD2) represent biologically interconnected stress-adaptation pathways that may contribute to tumor progression. However, their combined prognostic impact in TNBC remains insufficiently defined. This retrospective study included 70 patients with surgically treated TNBC. Immunohistochemical expression of HIF-1α (nuclear) and SOD2 (cytoplasmic) was semi-quantitatively scored and analyzed individually and in combination. Patients were stratified as both-low, single-high, or both-high expression. Associations with clinicopathological parameters were evaluated, and overall survival (OS) and disease-free survival (DFS) were analyzed using Kaplan-Meier and Cox regression models. Stage-adjusted and stage-free multivariable analyses were performed, and sensitivity analyses using penalized Cox regression were conducted. High SOD2 expression was observed in 68.6% and high HIF-1α expression in 24.3% of cases. Neither marker was independently associated with survival outcomes in Kaplan-Meier or multivariable analyses. HIF-1α-high tumors showed a nominally lower Ki-67 proliferation index compared with HIF-1α-low tumors (median 30.0% vs. 60.0%,

Indexed as

Hypoxia-Inducible Factor 1, alpha SubunitSuperoxide DismutaseTriple Negative Breast NeoplasmsAdultAgedBiomarkers, TumorDisease-Free SurvivalFemaleGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateMiddle AgedPrognosisRetrospective StudiesSuperoxide Dismutase 2Biomarkers, TumorHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitSuperoxide DismutaseSuperoxide Dismutase 2HIF-1αhypoxiaoxidative stressprognosisSOD2triple-negative breast cancer

Identifiers

PMID42353062
PMCPMC13299291

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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.