Evidence map›Paper›PMID 42226580›Full record

ArticleCancer medicine2026

Identification of Key Microbial Signatures Associated With Breast Cancer: Machine Learning-Based Approaches Using Gut Microbiome Data.

Md Tanvir Ahmed, Samriddha Majumdar, Abdullah Al Noman, Md Jahangir Alam, Md Jahangir Alam

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

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Md Tanvir AhmedDepartment of Genetic Engineering and Biotechnology, Shahjalal University of Science and Technology, Sylhet, Bangladesh.ORCID https://orcid.org/0009-0002-4274-1272
Samriddha MajumdarDepartment of Genetic Engineering and Biotechnology, Shahjalal University of Science and Technology, Sylhet, Bangladesh.
Abdullah Al NomanDepartment of Computer Science Engineering, Shahjalal University of Science and Technology, Sylhet, Bangladesh.
Md Jahangir AlamDepartment of Genetic Engineering and Biotechnology, Shahjalal University of Science and Technology, Sylhet, Bangladesh.
Md Jahangir AlamDepartment of Genetic Engineering and Biotechnology, Shahjalal University of Science and Technology, Sylhet, Bangladesh.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer (BC) is one of the most common types of cancer incidence and mortality rates among women all over the world. Limitations in existing diagnostic methods, especially in low- and middle-income countries, require novel, noninvasive biomarkers. A complex and modifiable ecosystem, the gut microbiome has become a potential origin of such biomarkers because it has a systemic influence on host immunity, metabolism, and regulation of hormones. This study explores the gut microbiome alterations associated with BC and evaluates machine learning (ML) models to predict disease status based on 16S rRNA gene sequencing data of Ghanaian cohort (520 BC patients, 442 healthy controls).

resultsFollowing high-quality sequence processing with QIIME2 and DADA2, alpha and beta diversity analyses showed a lower microbial richness and different community structures in BC patients (PERMANOVA, p = 0.001). Random Forest-based feature selection was used to find the top 20 discriminative genera, which were used to train 10 supervised ML algorithms. Ensemble models, particularly Random Forest, achieved the highest performance in predictive models (mean across 100 folds: AUC = 0.78, accuracy = 0.70), indicating strong discriminative potential. The results of SHAP analysis provided clear pictures of how specific microbes influence BC risk. We identified several risk-associated genera, notably Bacteroides, Lachnoclostridium, Parasutterella, and Tannerellaceae, whereas Coprococcus, Romboutsia, Ruminococcus, and Prevotella were associated with lower BC risk.

conclusionThis study reveals a clear shift in the gut microbiome community structure among BC patients. We identified specific bacterial genera that act as either elevated or decreased disease risk. These findings not only highlight the power of machine learning models for noninvasive risk prediction but also provide a foundation for novel microbiome-based diagnostic strategies.

Indexed as

BacteriaBreast NeoplasmsGastrointestinal MicrobiomeMachine LearningCase-Control StudiesFemaleHumansMiddle AgedPredictive Learning ModelsRandom ForestRNA, Ribosomal, 16SRNA, Ribosomal, 16S16S rRNAbreast cancerdiversity analysisdysbiosisgut microbiomemachine learningSHAP

Identifiers

PMID42226580
PMCPMC13238518

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