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A novel microRNA signature for pathological grading in?lung adenocarcinoma based on TCGA and GEO data

机译:基于TCGA和GEO数据的病理分级的一种新型MicroRNA签名

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Lung adenocarcinoma (LUAD) is one of the most common types of lung cancer and its poor prognosis largely depends on the tumor pathological stage. Critical roles of microRNAs (miRNAs) have been reported in the tumorigenesis and progression of lung cancer. However, whether the differential expression pattern of miRNAs could be used to distinguish early?stage (stage?I) from mid?late?stage (stages?II?IV) LUAD tumors is still unclear. In this study, clinical information and miRNA expression profiles of patients with LUAD were downloaded from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus databases. TCGA?LUAD (n=470) dataset was used for model training and validation, and the GSE62182 (n=94) and GSE83527 (n=36) datasets were used as external independent test datasets. The diagnostic model was created through miRNA feature selection followed by SVM classifier and was confirmed by 5?fold cross?validation. A receiver operating characteristic curve was calculated to evaluate the accuracy and robustness of the model. Using the DX score and LIBSVM tool, a 16?miRNA signature that could distinguish LUAD pathological stages was identified. The area under the curve rates were 0.62 [95% confidence interval (CI): 0.56?0.67], 0.66 (95% CI: 0.54?0.76) and 0.63 (95% CI: 0.43?0.82) in TCGA?LUAD internal validation dataset, the GSE62182 external validation dataset, and the GSE83527 external validation dataset, respectively. Kyoto Encyclopedia of Genes and Genomes and Gene Ontology enrichment analyses suggested that the target genes of the 16?miRNA signature were mainly involved in metabolic pathways. The present findings demonstrate that a 16?miRNA signature could serve as a promising diagnostic biomarker for pathological staging in LUAD.
机译:肺腺癌(路加)是最常见的肺癌类型之一,其预后的差主要取决于肿瘤病理阶段。 MicroRNAS(miRNA)的临界作用已在肿瘤癌症和肺癌进展中报道。然而,MIRNA的差异表达模式是否可用于区分早期?阶段(阶段?I)从中间?阶段(阶段?II?IV)管道肿瘤仍然不清楚。在该研究中,从癌症基因组地图集(​​TCGA)和基因表达综合数据库中下载了鲁拉患者的临床信息和miRNA表达谱。 TCGA?LUAD(n = 470)数据集用于模型训练和验证,而GSE62182(n = 94)和GSE83527(n = 36)数据集用作外部独立测试数据集。通过MiRNA特征选择,然后由SVM分类器进行诊断模型,并通过5?折叠十字架验证。计算接收器操作特性曲线以评估模型的精度和鲁棒性。使用DX得分和LIBSVM工具,确定了可以区分路障病理阶段的16?miRNA签名。曲线率下的面积为0.62 [95%置信区间(CI):0.56≤0.67],0.66(95%CI:0.54≤0.76)和0.63(95%CI:0.43?0.82)在TCGA中的内部验证数据集,GSE62182外部验证数据集和GSE83527外部验证数据集。基因和基因组的京都百科全书和基因本体浓缩分析表明,16?miRNA签名的靶基因主要参与代谢途径。本研究结果表明,16?miRNA签名可以作为管道的病理分期的有希望的诊断生物标志物。

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