Evidence map›Paper›PMID 39859358›Full record

ArticleInternational journal of molecular sciences2025

Implications of Mineralization Biomarkers in Breast Cancer Outcomes Beyond Calcifications.

Erica Giacobbi, Rita Bonfiglio, Gabriele Rotondaro, Francesca Servadei, Artem Smirnov, Valeria Palumbo, Maria Paola Scioli, Elena Bonanno, Claudio Oreste Buonomo, Gianluca Vanni and 3 more

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. PAX Family, Master Regulator in Cancer.Diagnostics (Basel, Switzerland) · 2025
    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

13 authors.

Erica GiacobbiDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", 00133 Rome, Italy.ORCID 0000-0002-2582-3527
Rita BonfiglioDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", 00133 Rome, Italy.
Gabriele RotondaroDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", 00133 Rome, Italy.ORCID 0009-0006-8555-3596
Francesca ServadeiDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", 00133 Rome, Italy.ORCID 0000-0003-2619-9153
Artem SmirnovDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", 00133 Rome, Italy.
Valeria PalumboDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", 00133 Rome, Italy.
Maria Paola ScioliDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", 00133 Rome, Italy.
Elena BonannoDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", 00133 Rome, Italy.
Claudio Oreste BuonomoBreast Unit, Department of Surgical Science, University of Rome "Tor Vergata", 00133 Rome, Italy.
Gianluca VanniBreast Unit, Department of Surgical Science, University of Rome "Tor Vergata", 00133 Rome, Italy.
Eleonora CandiDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", 00133 Rome, Italy.
Alessandro MaurielloDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", 00133 Rome, Italy.ORCID 0000-0002-7351-5676
Manuel ScimecaDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", 00133 Rome, Italy.ORCID 0000-0003-0585-1309

Funding

Ministero dell'Università e della Ricerca PRIN2022 2022TXHFSA
6 · The paper itself

Abstract

The aim of this work was to explore the biomarkers associated with epithelial to mesenchymal transition (EMT) and mineralization processes as new prognostic factors across different breast cancer phenotypes. To this end, 133 breast biopsies, including benign and malignant lesions, with or without microcalcifications, were retrospectively collected. Immunohistochemical analysis was performed to evaluate the expression of vimentin, BMP-2, BMP-4, RANKL, Runx2, OPN, PTX3, and SDF-1, while Kaplan-Meier plots were used to assess their prognostic impact on overall survival in a dataset of 2976 breast cancer patients. The expression of vimentin, BMP-2, BMP-4, and SDF-1 was significantly higher in malignant lesions compared to benign ones, regardless of the presence of microcalcifications. Notably, these markers showed no correlation with traditional prognostic factors, such as tumor grade or hormone receptor status. The bioinformatics analysis provided valuable insights into the possible prognostic and therapeutic significance of BMP-2, BMP-4, SDF-1, and vimentin in breast cancer. In fact, all these biomarkers impact on the overall survival in specific molecular breast cancer types. In addition, high expression of SDF-1 and vimentin is able to predict the response to chemotherapy. The findings here reported suggest that vimentin, BMP-2, BMP-4, and SDF-1 could be independent prognostic biomarkers in breast cancer, providing insights beyond traditional clinical factors.

Indexed as

Biomarkers, TumorBreast NeoplasmsCalcinosisAdultAgedBone Morphogenetic Protein 2Bone Morphogenetic Protein 4Chemokine CXCL12Epithelial-Mesenchymal TransitionFemaleHumansKaplan-Meier EstimateMiddle AgedPrognosisRetrospective StudiesVimentinBiomarkers, TumorBMP2 protein, humanBMP4 protein, humanBone Morphogenetic Protein 2Bone Morphogenetic Protein 4Chemokine CXCL12CXCL12 protein, humanVimentinbiomarkersBMP-2BMP-4breast cancerEMTmicrocalcificationsSDF-1vimentin

Identifiers

PMID39859358
PMCPMC11765781

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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.