Machine Learning-Based Genome-Wide Salivary DNA Methylation Analysis for Identification of Noninvasive Biomarkers in Oral Cancer Diagnosis

被引:11
|
作者
Adeoye, John [1 ]
Wan, Chi Ching Joan [1 ]
Zheng, Li-Wu [1 ]
Thomson, Peter [2 ]
Choi, Siu-Wai [1 ]
Su, Yu-Xiong [1 ]
机构
[1] Univ Hong Kong, Fac Dent, Div Oral & Maxillofacial Surg, Hong Kong 999077, Peoples R China
[2] James Cook Univ, Coll Med & Dent, Cairns, Qld 4870, Australia
关键词
biomarkers; diagnosis; DNA methylation; epigenomics; oral cancer; oral potentially malignant disorders; PROGNOSIS; MODEL;
D O I
10.3390/cancers14194935
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Because tissue biopsy is the gold standard for diagnosing oral cancer, it is often performed to confirm disease during screening, management, and monitoring. However, many reports are negative. Salivary biomarkers can provide the preliminary stratification of suspicious lesions to encourage patient selection in clinical practice. However, the discovery and implementation of salivary biomarkers still need to be refined. Therefore, in this study, we successfully utilized machine learning techniques to select optimal methylome biomarkers that may be applied for oral cancer diagnoses. This study aims to examine the feasibility of ML-assisted salivary-liquid-biopsy platforms using genome-wide methylation analysis at the base-pair and regional resolution for delineating oral squamous cell carcinoma (OSCC) and oral potentially malignant disorders (OPMDs). A nested cohort of patients with OSCC and OPMDs was randomly selected from among patients with oral mucosal diseases. Saliva samples were collected, and DNA extracted from cell pellets was processed for reduced-representation bisulfite sequencing. Reads with a minimum of 10x coverage were used to identify differentially methylated CpG sites (DMCs) and 100 bp regions (DMRs). The performance of eight ML models and three feature-selection methods (ANOVA, MRMR, and LASSO) were then compared to determine the optimal biomarker models based on DMCs and DMRs. A total of 1745 DMCs and 105 DMRs were identified for detecting OSCC. The proportion of hypomethylated and hypermethylated DMCs was similar (51% vs. 49%), while most DMRs were hypermethylated (62.9%). Furthermore, more DMRs than DMCs were annotated to promoter regions (36% vs. 16%) and more DMCs than DMRs were annotated to intergenic regions (50% vs. 36%). Of all the ML models compared, the linear SVM model based on 11 optimal DMRs selected by LASSO had a perfect AUC, recall, specificity, and calibration (1.00) for OSCC detection. Overall, genome-wide DNA methylation techniques can be applied directly to saliva samples for biomarker discovery and ML-based platforms may be useful in stratifying OSCC during disease screening and monitoring.
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页数:15
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