Evidence map›Paper›PMID 40362201›Full record

ArticleInternational journal of molecular sciences2025

Breast Cancer Stem Cells and Immunogenicity Profile in High-Risk Early Triple-Negative Breast Cancer: A Pilot Study.

Ariadna Roqué-Lloveras, Ferran Pérez-Bueno, Xavier Pozo-Ariza, Emma Polonio-Alcalá, Sira Ausellé-Bosch, Glòria Oliveras, Gemma Viñas, Teresa Puig

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Ariadna Roqué-LloverasMedical Oncology Department, Catalan Institute of Oncology Girona, 17007 Girona, Spain.ORCID 0000-0003-0492-7463
Ferran Pérez-BuenoNew Therapeutic Targets Laboratory (TargetsLab)-Oncology Unit, Medical Science Department, Faculty of Medicine, University of Girona, 17003 Girona, Spain.
Xavier Pozo-ArizaPathological Anatomy Department, Dr. Josep Trueta University Hospital, 17007 Girona, Spain.
Emma Polonio-AlcaláPrecision Oncology Group (OncoGIR-Pro), Institut d'Investigació Biomèdica de Girona (IDIBGI), 17190 Salt, Spain.ORCID 0000-0003-1017-7216
Sira Ausellé-BoschNew Therapeutic Targets Laboratory (TargetsLab)-Oncology Unit, Medical Science Department, Faculty of Medicine, University of Girona, 17003 Girona, Spain.ORCID 0009-0005-8284-4657
Glòria OliverasNew Therapeutic Targets Laboratory (TargetsLab)-Oncology Unit, Medical Science Department, Faculty of Medicine, University of Girona, 17003 Girona, Spain.
Gemma ViñasMedical Oncology Department, Catalan Institute of Oncology Girona, 17007 Girona, Spain.ORCID 0000-0002-0459-573X
Teresa PuigNew Therapeutic Targets Laboratory (TargetsLab)-Oncology Unit, Medical Science Department, Faculty of Medicine, University of Girona, 17003 Girona, Spain.ORCID 0000-0003-2715-7043

Funding

Fundació Oncolliga Girona ONCOSWIMINSTITUTO DE SALUD CARLOS III PI19/00372
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is an aggressive subtype requiring further knowledge of biomarkers to improve targeted therapy. A major resistance mechanism involves breast cancer stem cells (BCSCs) evading the immune system. Neoadjuvant or adjuvant chemotherapy may alter BCSCs and the patients' immune response. We conducted a retrospective study including 29 early-stage TNBC patients resistant to chemotherapy diagnosed at the Catalan Institute of Oncology (Girona, Spain) in 2010-2019. We obtained 44 paired tumor samples (pre- and post-chemotherapy) from the Tumor Biobank, assessing BCSC biomarkers (CD44, CD24, and ALDH1), PD-L1, and percentages of stromal tumor-infiltrating lymphocytes (TILs). Clinicopathological characteristics were also collected. At baseline, 68% of tumors had high CD44 expression, 55% showed low CD24 expression, 9% had high ALDH1 expression, 91% were PD-L1-negative (<1%), and 64% had a low percentage of stromal TILs. PD-L1 expression significantly increased post-chemotherapy, with 50% of initially negative tumors becoming PD-L1 positive (≥1%) (

Indexed as

Neoplastic Stem CellsTriple Negative Breast NeoplasmsAdultAgedAldehyde Dehydrogenase 1 FamilyB7-H1 AntigenBiomarkers, TumorCD24 AntigenFemaleHumansHyaluronan ReceptorsLymphocytes, Tumor-InfiltratingMiddle AgedPilot ProjectsRetinal DehydrogenaseRetrospective StudiesAldehyde Dehydrogenase 1 FamilyALDH1A1 protein, humanB7-H1 AntigenBiomarkers, TumorCD24 AntigenCD274 protein, humanHyaluronan ReceptorsRetinal Dehydrogenaseadjuvant chemotherapybreast cancer stem cellsneoadjuvant chemotherapyPD-L1targeted therapytriple-negative breast cancer

Identifiers

PMID40362201
PMCPMC12071224

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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.