Evidence map›Paper›PMID 39242600›Full record

ArticleNPJ breast cancer2024

GATA3 and markers of epithelial-mesenchymal transition predict long-term benefit from tamoxifen in ER-positive breast cancer.

Josefine Sandström, Jens Bomanson, Gizeh Pérez-Tenorio, Carolin Jönsson, Bo Nordenskjöld, Tommy Fornander, Linda S Lindström, Olle Stål

Abstract read
In one paragraph

Article in NPJ breast cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Game of clones: decipher lineage plasticity in hormone-driven cancers.Cellular and molecular life sciences : CMLS · 2026
    Review
  4. Review
  5. Article
  6. Article
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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

8 authors.

Josefine SandströmDepartment of Biomedical and Clinical Sciences and Department of Oncology, 581 83 Linköping University, Linköping, Sweden.
Jens BomansonDepartment of Biomedical and Clinical Sciences and Department of Oncology, 581 83 Linköping University, Linköping, Sweden.
Gizeh Pérez-TenorioDepartment of Biomedical and Clinical Sciences and Department of Oncology, 581 83 Linköping University, Linköping, Sweden.
Carolin JönssonDepartment of Biomedical and Clinical Sciences and Department of Oncology, 581 83 Linköping University, Linköping, Sweden.
Bo NordenskjöldDepartment of Biomedical and Clinical Sciences and Department of Oncology, 581 83 Linköping University, Linköping, Sweden.
Tommy FornanderDepartment of Oncology and Pathology, Karolinska Institute and University Hospital, Stockholm, Sweden.
Linda S LindströmDepartment of Oncology and Pathology, Karolinska Institute and University Hospital, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-7722-7532
Olle StålDepartment of Biomedical and Clinical Sciences and Department of Oncology, 581 83 Linköping University, Linköping, Sweden. olle.stal@liu.se.ORCID http://orcid.org/0000-0002-8290-0592

Funding

Cancerfonden (Swedish Cancer Society) 222081 and 220552SIAVetenskapsrådet (Swedish Research Council) 2020-02466
6 · The paper itself

Abstract

GATA binding protein 3 (GATA3) is essential for normal development of the mammary gland and associated with ER-positive breast cancer. Loss of GATA3 has been associated with epithelial-mesenchymal transition (EMT) in experimental studies. We investigated tumoral GATA3 in a cohort of postmenopausal patients with lymph-node negative breast cancer, randomized to adjuvant tamoxifen or control. Nuclear GATA3 expression was assessed with immunohistochemistry and GATA3 gene expression with Agilent microarrays. High GATA3 nuclear expression was associated with a lower rate of distant recurrence in ER-positive breast cancer (HR = 0.60, 95% CI 0.39-0.93). Low gene expression of GATA3 was associated with limited long-term benefit from adjuvant tamoxifen (interaction: p = 0.033). GATA3 gene expression was associated with the epithelial markers CDH1 (E-cadherin) and FOXA1, whereas negatively associated with several mesenchymal markers. Low expression of CDH1 was associated with marginal tamoxifen benefit (HR = 0.80 (0.43-1.49)), whereas patients with higher expression showed a significant benefit (HR = 0.33 (0.20-0.55), interaction: p = 0.029). In ER-positive breast cancer, diminished expression of GATA3 is associated with markers of EMT and poor long-term benefit from tamoxifen.

Identifiers

PMID39242600
PMCPMC11379893

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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.