| Literature DB >> 34359669 |
Vijayachitra Modhukur1,2, Shakshi Sharma3, Mainak Mondal1, Ankita Lawarde1,2, Keiu Kask1,2, Rajesh Sharma3, Andres Salumets1,2,4.
Abstract
Metastatic cancers account for up to 90% of cancer-related deaths. The clear differentiation of metastatic cancers from primary cancers is crucial for cancer type identification and developing targeted treatment for each cancer type. DNA methylation patterns are suggested to be an intriguing target for cancer prediction and are also considered to be an important mediator for the transition to metastatic cancer. In the present study, we used 24 cancer types and 9303 methylome samples downloaded from publicly available data repositories, including The Cancer Genome Atlas (TCGA) and the Gene Expression Omnibus (GEO). We constructed machine learning classifiers to discriminate metastatic, primary, and non-cancerous methylome samples. We applied support vector machines (SVM), Naive Bayes (NB), extreme gradient boosting (XGBoost), and random forest (RF) machine learning models to classify the cancer types based on their tissue of origin. RF outperformed the other classifiers, with an average accuracy of 99%. Moreover, we applied local interpretable model-agnostic explanations (LIME) to explain important methylation biomarkers to classify cancer types.Entities:
Keywords: DNA methylation; TCGA; artificial intelligence; biomarkers; clustering; differential methylation; epigenetics; explainable predictions; machine learning; metastasis
Year: 2021 PMID: 34359669 DOI: 10.3390/cancers13153768
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639