Du Hailei, Xie Shanshan, Guo Wei, Che Jiaming, Zhu Lianggang, Hang Junbiao, Li Hecheng
Department of Thoracic Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Ann Transl Med. 2021 Feb;9(4):317. doi: 10.21037/atm-20-4541.
Autophagy has a dual function in cancer, and its role in carcinogenesis of the esophagus remains poorly understood. In the present study, we explored the prognostic value of autophagy in esophageal cancer (ESCA), one of the leading causes of cancer-related deaths worldwide.
Using ESCA RNA-sequencing (RNA-Seq) data from 158 primary patients with ESCA, including esophageal adenocarcinoma and esophageal squamous cell carcinoma, were downloaded from The Cancer Genome Atlas (TCGA) for this study. We obtained differentially expressed autophagy-related genes (ARGs) by the "limma" package of R. The Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genome (KEGG) analyses unveiled several fundamental signaling pathways associated with the differentially expressed ARGs in ESCA. Univariate Cox regression analyses were used to estimate associations between ARGs and overall survival (OS) in the TCGA ESCA cohort. A Cox proportional hazards model (iteration =1,000) with a lasso penalty was used to create the optimal multiple-gene prognostic signature utilizing an R package called "glmnet".
A prognostic signature was constructed with four ARGs (, , and ) in the training set, which significantly divided ESCA patients into high- and low-risk groups in terms of OS [hazard ratio (HR) =1.508, 95% confidence interval (CI): 1.201-1.894, P<0.001]. In the testing set, the risk score remained an independent prognostic factor in the multivariate analyses (HR =1.572, 95% CI: 1.096-2.257, P=0.014). The area under the curve (AUC) of the receiver operating characteristic (ROC) predicting 1-year survival showed a better predictive power for the prediction model. The AUC in training and testing cohorts were 0.746 and 0.691, respectively. Therefore, the prognostic signature of the four ARGs was successfully validated in the independent cohort.
The prognostic signature may be an independent predictor of survival for ESCA patients. The prognostic nomogram may improve the prediction of individualized outcome. This study also highlights the importance of autophagy in the outcomes of patients with ESCA.
自噬在癌症中具有双重作用,其在食管癌发生中的作用仍知之甚少。在本研究中,我们探讨了自噬在食管癌(ESCA)中的预后价值,食管癌是全球癌症相关死亡的主要原因之一。
本研究从癌症基因组图谱(TCGA)下载了158例原发性ESCA患者(包括食管腺癌和食管鳞状细胞癌)的ESCA RNA测序(RNA-Seq)数据。我们通过R语言的“limma”包获得差异表达的自噬相关基因(ARG)。基因本体(GO)和京都基因与基因组百科全书(KEGG)分析揭示了与ESCA中差异表达的ARG相关的几个基本信号通路。单变量Cox回归分析用于估计TCGA ESCA队列中ARG与总生存期(OS)之间的关联。使用带有套索惩罚的Cox比例风险模型(迭代=1000),利用名为“glmnet”的R包创建最佳多基因预后特征。
在训练集中用四个ARG构建了一个预后特征,根据OS将ESCA患者显著分为高风险组和低风险组[风险比(HR)=1.508,95%置信区间(CI):1.201-1.894,P<0.001]。在测试集中,风险评分在多变量分析中仍然是一个独立的预后因素(HR =1.572,95%CI:1.096-2.257,P=0.014)。预测1年生存期的受试者工作特征(ROC)曲线下面积(AUC)显示预测模型具有更好的预测能力。训练集和测试集中的AUC分别为0.746和0.691。因此,四个ARG的预后特征在独立队列中得到成功验证。
该预后特征可能是ESCA患者生存的独立预测指标。预后列线图可能会改善个体预后的预测。本研究还强调了自噬在ESCA患者预后中的重要性。