Shi Xiaoshun, Tan Haoming, Le Xiaobing, Xian Haibing, Li Xiaoxiang, Huang Kailing, Luo Viola Yingjun, Liu Yanhui, Wu Zhuolin, Mo Haiyun, Chen Allen M, Liang Ying, Zhang Jiexia
National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Department of Medicine, Guangzhou Institute of Respiratory Disease, Guangzhou Institute of Respiratory Health, Guangzhou 510120, China,
Department of Thoracic Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Cancer Manag Res. 2018 Sep 24;10:3717-3732. doi: 10.2147/CMAR.S159563. eCollection 2018.
The current TNM staging system plays a central role in lung adenocarcinoma (LUAD) prognosis. However, it may not adequately stratify the risk of tumor recurrence. With the aid of gene expression profiling, we identified 31 lncRNAs whose expressions in tumor tissues could be used as a risk indicator for the guidance of lung cancer therapy. This exploratory analysis may shed new light on identification of potential prognostic factors.
A survival prediction scoring model was developed from the data that are publicly available in The Cancer Genome Atlas (TCGA) LUAD RNA Sequencing dataset. Multivariate Cox regression analysis and Kaplan-Meier analysis were performed on a cohort of 254 stage I lung carcinoma patients with survival records.
Our model indicates that the panels comprising 31 lncRNAs are highly associated with overall survival (OS): 18.9% (95% CI: 10.4%-34.5%) and 89.5% (95% CI: 80.7%-99.2%) for the high- and low-risk group, respectively. The specificity and sensitivity of the model are verified, which show that the area under receiver operating characteristic curve yields 0.881, meaning our model has good accuracy and it is feasible for further applications.
The 31-lncRNA model might be able to predict OS in patients with LUAD with high accuracy. Its further applications in biomolecular experiments using clinical samples with independent cohorts of patients are needed to verify the results.
目前的TNM分期系统在肺腺癌(LUAD)预后评估中起着核心作用。然而,它可能无法充分分层肿瘤复发风险。借助基因表达谱分析,我们鉴定出31种lncRNA,其在肿瘤组织中的表达可作为肺癌治疗指导的风险指标。这项探索性分析可能为潜在预后因素的识别提供新线索。
基于癌症基因组图谱(TCGA)LUAD RNA测序数据集中公开可用的数据,开发了一种生存预测评分模型。对254例有生存记录的I期肺癌患者队列进行多变量Cox回归分析和Kaplan-Meier分析。
我们的模型表明,由31种lncRNA组成的面板与总生存期(OS)高度相关:高风险组和低风险组的OS分别为18.9%(95%CI:10.4%-34.5%)和89.5%(95%CI:80.7%-99.2%)。验证了模型的特异性和敏感性,结果显示受试者工作特征曲线下面积为0.881,这意味着我们的模型具有良好的准确性,并且进一步应用是可行的。
31-lncRNA模型可能能够高精度预测LUAD患者的OS。需要在使用独立患者队列的临床样本的生物分子实验中进一步应用该模型以验证结果。