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首页> 外文期刊>Thoracic cancer. >Integrative analysis of differential genes and identification of a “2‐gene score” associated with survival in esophageal squamous cell carcinoma
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Integrative analysis of differential genes and identification of a “2‐gene score” associated with survival in esophageal squamous cell carcinoma

机译:食管鳞状细胞癌差异基因的综合分析和与生存相关的“ 2基因评分”的鉴定

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Background Developments in high‐throughput genomic technologies have led to improved understanding of the molecular underpinnings of esophageal squamous cell carcinoma (ESCC). However, there is currently no model that combines the clinical features and gene expression signatures to predict outcomes. Methods We obtained data from the GSE53625 database of Chinese ESCC patients who had undergone surgical treatment. The R packages, Limma and WGCNA, were used to identify and construct a co‐expression network of differentially expressed genes, respectively. The Cox regression model was used, and a nomogram prediction model was constructed. Results A total of 3654 differentially expressed genes were identified. Bioinformatics enrichment analysis was conducted. Multivariate analysis of the clinical cohort revealed that age and adjuvant therapy were independent factors for survival, and these were entered into the clinical nomogram. After integrating the gene expression profiles, we identified a “2‐gene score” associated with overall survival. The combinational model is composed of clinical data and gene expression profiles. The C‐index of the combined nomogram for predicting survival was statistically higher than the clinical nomogram. The calibration curve revealed that the combined nomogram and actual observation showed better prediction accuracy than the clinical nomogram alone. Conclusions The integration of gene expression signatures and clinical variables produced a predictive model for ESCC that performed better than those based exclusively on clinical variables. This approach may provide a novel prediction model for ESCC patients after surgery.
机译:背景高通量基因组技术的发展导致人们对食管鳞状细胞癌(ESCC)的分子基础有了更深入的了解。但是,目前尚无模型可结合临床特征和基因表达特征来预测结果。方法我们从GSE53625数据库中获得了接受手术治疗的中国ESCC患者的数据。 R软件包Limma和WGCNA分别用于鉴定和构建差异表达基因的共表达网络。使用Cox回归模型,并构建了列线图预测模型。结果共鉴定出3654个差异表达基因。进行了生物信息学富集分析。临床队列的多变量分析显示,年龄和辅助治疗是生存的独立因素,这些因素已纳入临床列线图。整合基因表达谱后,我们确定了与总体存活率相关的“ 2-基因评分”。组合模型由临床数据和基因表达谱组成。组合诺模图用于预测生存的C指数在统计学上高于临床诺模图。校准曲线显示,组合的列线图和实际观察结果显示比单独的临床列线图更好的预测准确性。结论基因表达特征和临床变量的整合产生了ESCC的预测模型,该模型的效果优于仅基于临床变量的预测模型。该方法可以为ESCC患者术后提供新颖的预测模型。

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