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Identification of Serum MicroRNAs as Novel Biomarkers in Esophageal Squamous Cell Carcinoma Using Feature Selection Algorithms

机译:使用特征选择算法识别食管鳞状细胞癌中作为新生物标记物的血清微小RNA

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摘要

>Introduction: Circulating microRNAs (miRNAs) are promising molecular biomarkers for the early detection of esophageal squamous cell carcinoma (ESCC). We investigated the serum miRNA expression profiles from microarray-based technologies and evaluated the diagnostic value of serum miRNAs as potential biomarkers for ESCC by using feature selection algorithms.>Methods: Serum miRNA expression profiles were obtained from 52 ESCC patients and 52 age- and sex-matched controls via performing a high-throughput microarray assay. Five representative feature selection algorithms including the false discovery rate procedure, family-wise error rate procedure, Lasso logistic regression, hybrid huberized support vector machine (SVM), and SVM using the squared-error loss with the elastic-net penalty were jointly carried out to select the significantly differentially expressed miRNAs based on the miRNA profiles.>Results: Three miRNAs including miR-16-5p, miR-451a, and miR-574-5p were identified as the powerful biomarkers for the diagnosis of ESCC. The diagnostic accuracy of the combination of these three miRNAs was evaluated by using logistic regression and the SVM. The averages of the area under the receiver operating curve and classification accuracies based on different classifiers were more than 0.80 and 0.79, respectively. The cross-validation results suggested that the three-miRNA-based classifiers could clearly distinguish ESCC patients from healthy controls. Moreover, the classifying performance of the miRNA panel persisted in discriminating the healthy group from patients with ESCC stage I-II (AUC > 0.76) and patients with ESCC stage III-IV (AUC > 0.80).>Conclusions: These results in this study have moved forward the identification of novel biomarkers for the diagnosis of ESCC.
机译:>简介:循环microRNA(miRNA)是用于早期发现食管鳞状细胞癌(ESCC)的有前途的分子生物标记。我们研究了基于微阵列技术的血清miRNA表达谱,并通过特征选择算法评估了血清miRNA作为ESCC潜在生物标志物的诊断价值。>方法:从52位ESCC患者中获得了血清miRNA表达谱。和52个年龄和性别匹配的对照通过执行高通量微阵列分析。联合执行了五种代表性特征选择算法,包括错误发现率过程,家庭式错误率过程,Lasso logistic回归,混合Huberized支持向量机(SVM)和使用平方误差损失和弹性网罚的SVM。根据miRNA图谱选择差异显着表达的miRNA。>结果:鉴定出miR-16-5p,miR-451a和miR-574-5p这三种miRNA是诊断的有力生物标记ESCC。这三种miRNA组合的诊断准确性通过逻辑回归和SVM进行了评估。接收器工作曲线下的面积平均值和基于不同分类器的分类精度分别大于0.80和0.79。交叉验证结果表明,基于三个miRNA的分类器可以清楚地区分ESCC患者和健康对照者。此外,miRNA小组的分类性能仍然可以将健康组与ESCC I-II期(AUC> 0.76)和ESCC III-IV期(AUC> 0.80)的患者区分开。>结论:这项研究中的这些结果推动了用于诊断ESCC的新型生物标志物的鉴定。

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