bioRxivBioinformaticsPreprint
Machine Learning Methods to Identify Genetic Correlates of Radiation-Associated Contralateral Breast Cancer in the WECARE Study
Sangkyu LeeiD, Xiaolin LiangiD, Meghan WoodsiD, Anne S. ReineriD, Duncan C. ThomasiD, PATRICK J. CONCANNONiD, Leslie BernsteiniD, Charles F. LynchiD, John D. BoiceiD, Joseph O. DeasyiD, Jonine L. BernsteiniD, Jung Hun OhiD
Abstract
The purpose of this study is to identify germline single nucleotide polymorphisms (SNPs) that optimally predict radiation-associated contralateral breast cancer (RCBC) and to provide new biological insights into the carcinogenic process. Fifty-two women with contralateral breast cancer and 153 women with unilateral breast cancer were identified within the Womens Environmental Cancer and Radiation Epidemiology (WECARE) Study who were at increased risk of RCBC because they were [≤] 40 years of age at first diagnosis of breast cancer and received a scatter radiation dose > 1 Gy to the contralateral breast. A previously reported algorithm, preconditioned random forest regression, was applied to predict the risk of developing RCBC. The resulting model produced an area under the curve of 0.62 (p=0.04) on hold-out validation data. The biological analysis identified the cyclic AMP-mediated signaling and Ephrin-A as significant biological correlates, which were previously shown to influence cell survival after radiation in an ATM-dependent manner. The key connected genes and proteins that are identified in this analysis were previously identified as relevant to breast cancer, radiation response, or both. In summary, machine learning/bioinformatics methods applied to genome-wide genotyping data have great potential to reveal plausible biological correlates associated with the risk of RCBC.
- organism: human
- assay: GWAS summary statistics
- research focus: differential expression
- research focus: gene regulatory network inference
- research focus: benchmarking
- approach: machine learning (classical)
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Gene-level germline contributions to clinical risk of recurrence scores in Black and White breast cancer patients
Achal Patel, Montserrat García‐Closas, … Arjun Bhattacharya·Cancer ResearchPeer-reviewed·Oct 28, 2021
- Germline Allelic Expression of Genes at 17q22 Locus Associates with Risk of Breast Cancer
Filipa Esteves, Joana M. Xavier, … Ana-Teresa Maia·European Journal of CancerPeer-reviewed·Jun 27, 2022
- Coffee consumption and risk of breast cancer: a Mendelian Randomization study
M. Ellingjord-Dale, N. P. Papadimitriou, … K. K. Tsilidis·bioRxiv·Jul 17, 2020
- Correlation between DNA double strand breaks and cell death in peripheral blood lymphocytes from breast cancer patients
Ángela Solana-Peña, Mònica Pujol-Canadell, … Joan Francesc Barquinero·International Journal of Radiation BiologyPeer-reviewed·Sep 2, 2025
- New single nucleotide polymorphisms (SNPs) in homologous recombination repair genes detected by microarray analysis in Polish breast cancer patients
Hanna Romanowicz, Dominik Strapagiel, … Beata Smolarz·Clinical and Experimental MedicinePeer-reviewed·Nov 30, 2016
- Pre-diagnosis blood DNA methylation profiling of twin pairs discordant for breast cancer points to the importance of environmental risk
Hannes Frederik Bode, Liang He, … Miina Ollikainen·Clinical EpigeneticsPeer-reviewed·Nov 18, 2024