Evidence map›Paper›PMID 41366803›Full record

ArticleBreast cancer research : BCR2025

APOBEC3B protein expression associates with poor prognosis for breast cancer patients with ER-positive disease.

Maartje A C Schreurs, A Mieke Timmermans, Michael A Carpenter, Marcel Smid, Michael A den Bakker, Carolien H M van Deurzen, Reuben S Harris, John W M Martens

Abstract read
In one paragraph

Article in Breast cancer research : BCR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Maartje A C Schreurs *Department of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.
A Mieke Timmermans *Department of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.
Michael A CarpenterDepartment of Biochemistry and Structural Biology, University of Texas Health San Antonio, San Antonio, Texas, 78229, USA.
Marcel SmidDepartment of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.
Michael A den BakkerDepartment of Pathology, Maasstad Hospital, Rotterdam, The Netherlands.
Carolien H M van DeurzenDepartment of Pathology, Erasmus MC Cancer Institute, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Reuben S HarrisDepartment of Biochemistry and Structural Biology, University of Texas Health San Antonio, San Antonio, Texas, 78229, USA.
John W M MartensDepartment of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands. j.martens@erasmusmc.nl.

Funding

Targeting Polθ to Overcome PARP Inhibitor Resistance in Homologous Recombination Deficient Breast CancerP50CA247749 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Sarat Chandarlapaty, Simon N. Powell · 2020 to 2026
$16.3M
PROJECT 3 – BIOLOGY OF DNA DEAMINASES IN CANCERP01CA234228 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Michael Allen Carpenter · 2019 to 2026
$14.5M
NCI NIH HHS P01 CA234228NCI NIH HHS P50 CA247749
6 · The paper itself

Abstract

APOBEC enzymes, including APOBEC3B (A3B), have been linked to recurrent mutational patterns in breast cancers (BC). Currently, there is considerable level of evidence that A3B mRNA expression is associated with poor prognosis in ER-positive BC. Since the clinical relevance of A3B at the protein level has not been well studied, we evaluated A3B protein expression by immunohistochemistry on tumor tissue microarrays. Samples from 646 invasive, non-metastatic primary ER-positive BC patients who did not receive any systemic endocrine therapy as standard of care treatment, allowed us to study the pure prognostic impact of A3B protein expression on disease-free survival (DFS), metastatic disease-free survival (MFS), breast cancer specific-survival (BCSS), and overall survival (OS). Furthermore, 220 tumor specimens from BC patients who relapsed and did receive tamoxifen as first-line palliative treatment were included to study the association of A3B protein expression and progression free survival (PFS). Cox regression models were used to determine the impact of A3B protein expression on prognosis and PFS. We found that A3B expression associates with larger and higher grade tumors. Furthermore, univariable analyses showed that high A3B expression was associates with a shorter DFS (HR = 1.68; 95%CI = 1.31–2.14), MFS (HR = 1.93; 95%CI = 1.45–2.56), BCSS (HR = 2.72; 95%CI = 1.89–3.90), and OS (HR = 1.89; 95%CI = 1.40–2.56). Also, a shorter PFS (HR = 1.41; 95%CI = 1.03–1.92) was found. After adjustment for confounders, the observed associations remained significant. To conclude, in ER-positive BC, A3B protein expression is a marker for poor disease outcome and for rapid progression during endocrine treatment.

Indexed as

Biomarkers, TumorBreast NeoplasmsCytidine DeaminaseMinor Histocompatibility AntigensReceptors, EstrogenAdultAgedDisease-Free SurvivalFemaleHumansImmunohistochemistryMiddle AgedPrognosisTamoxifenAPOBEC3B protein, humanBiomarkers, TumorCytidine DeaminaseMinor Histocompatibility AntigensReceptors, EstrogenTamoxifen

Identifiers

PMID41366803
PMCPMC12802011

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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.