Evidence map›Paper›PMID 41118384›Full record

SynthesisPloS one2025

Prognostic value of FOXA1 in estrogen receptor-negative breast cancer: A systematic review and meta-analysis.

Angela V Fonseca-Benitez, David Díaz-Báez, James Guevara-Pulido, Milena Rondón-Lagos, Andrés Felipe Aristizábal-Pachón, Nelson Rangel

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in PloS one, 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

6 authors.

Angela V Fonseca-BenitezDepartamento de Nutrición y Bioquímica, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá, Colombia.ORCID https://orcid.org/0000-0002-4471-4115
David Díaz-BáezUniversidad El Bosque, School of Dentistry, Unit of Basic Oral Investigation - UIBO, Bogotá, Colombia.
James Guevara-PulidoUniversidad El Bosque, Facultad de Ciencias, INQA-Química Farmacéutica, Bogotá, Colombia.ORCID https://orcid.org/0000-0001-9134-3719
Milena Rondón-LagosSchool of Biological Sciences, Universidad Pedagógica y Tecnológica de Colombia, Tunja, Colombia.
Andrés Felipe Aristizábal-PachónDepartamento de Nutrición y Bioquímica, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá, Colombia.
Nelson RangelDepartamento de Nutrición y Bioquímica, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá, Colombia.ORCID https://orcid.org/0000-0002-9709-2196

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer remains the most common cancer among women worldwide, and recurrence rates stay high despite current treatments, especially for those with negative estrogen receptor status, where therapies are less effective, and prognosis is worse. Identifying molecules with predictive value for therapy response and prognosis is therefore crucial. In this context, FOXA1 could serve as a potential biomarker to predict the progression of ER-negative tumors. A search was conducted to answer the question, "What is the prognostic value of FOXA1 expression in breast cancer, estrogen receptor negative?" using various databases. Controlled vocabulary and Boolean operators were employed. Only studies reporting overall survival and disease-free survival, defined as the time from evaluation to death or relapse, were included. We identified seven articles evaluating FOXA1 and its relationship with disease-free survival (DFS) or overall survival (OS) in patients with ER-negative breast cancer. Our data indicate that higher FOXA1 expression is associated with improved overall survival (HR = 0.61, CI = 0.45-0.83, p < 0.002) and better disease-free survival (HR = 0.69, CI = 0.51-0.93, p < 0.02). These findings suggest that FOXA1 is linked to a favorable prognosis in terms of overall survival and disease-free survival. Further studies are needed to assess the role of FOXA1 in response to chemotherapy. PROSPERO registration number: CRD42024453750.

Indexed as

Biomarkers, TumorBreast NeoplasmsHepatocyte Nuclear Factor 3-alphaReceptors, EstrogenDisease-Free SurvivalFemaleHumansPrognosisBiomarkers, TumorFOXA1 protein, humanHepatocyte Nuclear Factor 3-alphaReceptors, Estrogen

Identifiers

PMID41118384
PMCPMC12539746

What OpenQuestion holds

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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.