Evidence map›Paper›PMID 41547953›Full record

ArticleScientific reports2026

Low tumoral Trefoil Factor 1 expression relates to aggressive tumor features and poor survival in young women with breast cancer.

Amalie B Kvamme, Ulrikke Hugaas, Anna K M Sæle, Lise M Ingebriktsen, Amalie A Svanøe, Rasmus O C Humlevik, Ingeborg Winge, Turid Aas, Anette Heie, Lars A Akslen and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 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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0cells of the map it votes in
0citing papers in PubMed
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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.

Amalie B KvammeCentre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, N-5021, Bergen, Norway.
Ulrikke HugaasCentre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, N-5021, Bergen, Norway.
Anna K M SæleCentre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, N-5021, Bergen, Norway.
Lise M IngebriktsenCentre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, N-5021, Bergen, Norway.
Amalie A SvanøeCentre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, N-5021, Bergen, Norway.
Rasmus O C HumlevikCentre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, N-5021, Bergen, Norway.
Ingeborg WingeCentre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, N-5021, Bergen, Norway.
Turid AasDepartment of Surgery, Haukeland University Hospital, Bergen, Norway.
Anette HeieDepartment of Surgery, Haukeland University Hospital, Bergen, Norway.
Lars A AkslenCentre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, N-5021, Bergen, Norway.
Erling A Hoivik *Centre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, N-5021, Bergen, Norway.
Elisabeth Wik *Centre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, N-5021, Bergen, Norway. Elisabeth.Wik@uib.no.ORCID http://orcid.org/0000-0002-5069-5715

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In young breast cancer (BC) patients, there is a need for additional biomarkers beyond those currently available. Trefoil Factor 1 (TFF1) is an estrogen-regulated protein with proposed prognostic relevance in BC. We assessed TFF1 protein expression by immunohistochemistry (IHC) in biopsies from patients with primary breast cancer diagnosed before age 50 and their paired axillary lymph node (LN) metastases within our in-house Bergen Young BC Cohort (n = 319). In addition, TFF1 mRNA levels and associated gene expression patterns were analyzed using publicly available datasets, including the Molecular Taxonomy of Breast Cancer International Consortium (METABRIC, n = 939) and the Cancer Cell Line Encyclopedia (n = 47). Our aim was to investigate how TFF1 expression in primary tumors (PT) and paired LN metastases relates to age at diagnosis, clinico-pathological features, and disease-specific survival, and to explore TFF1-associated gene expression profiles. Low TFF1 protein and mRNA expression in PTs was associated with younger age, aggressive clinico-pathologic features, and poorer survival. Additionally, TFF1 mRNA expression was a strong predictor of the basal-like subtype, and TFF1-low tumors exhibited stem-like characteristics, upregulation of immune checkpoints, and higher proliferation scores. In LN metastases, low TFF1 protein expression was associated with aggressive tumor features. Notably, high TFF1 protein expression in LN metastases predicted poorer survival in patients under 40 years. Our results indicate that low BC TFF1 expression is associated with younger age and aggressive tumor features, on top of serving as a predictor of the basal-like subtype. High TFF1 protein expression in LN metastases may carry prognostic significance for younger patients.

Indexed as

Biomarkers, TumorBreast NeoplasmsTrefoil Factor-1AdultFemaleGene Expression Regulation, NeoplasticHumansImmunohistochemistryLymphatic MetastasisMiddle AgedPrognosisRNA, MessengerBiomarkers, TumorRNA, MessengerTFF1 protein, humanTrefoil Factor-1Breast cancerSurvivalTFF1Young age

Identifiers

PMID41547953
PMCPMC12891483

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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.