Evidence map›Paper›PMID 41562101›Full record

ArticleCancer informatics2026

Prospective Breast Cancer Biomarkers Identified Using miR-526b-Driven Metabolic Alterations.

Braydon Nault, Mousumi Majumder

Abstract read
In one paragraph

Article in Cancer informatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

2 authors.

Braydon NaultDepartment of Biology, Brandon University, MB, Canada.
Mousumi MajumderDepartment of Biology, Brandon University, MB, Canada.ORCID https://orcid.org/0000-0003-0485-5172

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Breast cancer is a heterogeneous disease driven by dysregulated cellular processes, including altered metabolic pathways. The oncogenic microRNA miR-526b influences several cancer hallmark phenotypes and holds promise as a plasma biomarker. Given miR-526b's role in metabolic regulation, we have decided Methods: We analyzed mRNA expression of these 4 metabolic markers in breast cancer tissue biopsies and plasma samples from patients and disease-free controls, using publicly available datasets and RT-qPCR validation. Diagnostic performance was evaluated using univariate and multivariate logistic regression and LASSO regression modeling. The potential of combining Results: Individually, none of the metabolic markers demonstrated sufficient sensitivity or specificity as plasma biomarkers. However, combining markers via logistic and LASSO regression improved classification performance. Conclusions: Our study validates the potential of miR-526b-regulated metabolic genes as complementary breast cancer biomarkers. While

Indexed as

ATP5A1biomarkerbreast cancermetabolismmiR-526b

Identifiers

PMID41562101
PMCPMC12813260

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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.