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Machine learning unveils an immune-related DNA methylation profile in germline DNA from breast cancer patients

Authors :
Ning Yuan Lee
Melissa Hum
Guek Peng Tan
Ai Choo Seah
Pei-Yi Ong
Patricia T. Kin
Chia Wei Lim
Jens Samol
Ngiap Chuan Tan
Hai-Yang Law
Min-Han Tan
Soo-Chin Lee
Peter Ang
Ann S. G. Lee
Source :
Clinical Epigenetics, Vol 16, Iss 1, Pp 1-11 (2024)
Publication Year :
2024
Publisher :
BMC, 2024.

Abstract

Abstract Background There is an unmet need for precise biomarkers for early non-invasive breast cancer detection. Here, we aimed to identify blood-based DNA methylation biomarkers that are associated with breast cancer. Methods DNA methylation profiling was performed for 524 Asian Chinese individuals, comprising 256 breast cancer patients and 268 age-matched healthy controls, using the Infinium MethylationEPIC array. Feature selection was applied to 649,688 CpG sites in the training set. Predictive models were built by training three machine learning models, with performance evaluated on an independent test set. Enrichment analysis to identify transcription factors binding to regions associated with the selected CpG sites and pathway analysis for genes located nearby were conducted. Results A methylation profile comprising 51 CpGs was identified that effectively distinguishes breast cancer patients from healthy controls achieving an AUC of 0.823 on an independent test set. Notably, it outperformed all four previously reported breast cancer-associated methylation profiles. Enrichment analysis revealed enrichment of genomic loci associated with the binding of immune modulating AP-1 transcription factors, while pathway analysis of nearby genes showed an overrepresentation of immune-related pathways. Conclusion This study has identified a breast cancer-associated methylation profile that is immune-related to potential for early cancer detection.

Details

Language :
English
ISSN :
18687083
Volume :
16
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Clinical Epigenetics
Publication Type :
Academic Journal
Accession number :
edsdoj.172b376676d4fff8bb751ff838dda6c
Document Type :
article
Full Text :
https://doi.org/10.1186/s13148-024-01674-2