Machine learning on genome-wide association studies to predict the risk of radiation-associated contralateral breast cancer in the WECARE Study.
Sangkyu LeeXiaolin LiangMeghan WoodsAnne S ReinerPatrick ConcannonLeslie BernsteinCharles F LynchJohn D BoiceJoseph O DeasyJonine L BernsteinJung Hun OhPublished in: PloS one (2020)
The purpose of this study was 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 Women's 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 (AUC) 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.
Keyphrases
- genome wide
- machine learning
- dna methylation
- big data
- artificial intelligence
- genome wide association
- single cell
- breast cancer risk
- electronic health record
- pregnant women
- radiation therapy
- radiation induced
- risk factors
- stem cells
- deep learning
- type diabetes
- copy number
- bone marrow
- insulin resistance
- skeletal muscle
- gene expression
- dna damage response
- lymph node metastasis
- bioinformatics analysis