Department of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, China.
Department of Respiratory and Critical Care Medicine, Qilu Hospital of Shandong University, Jinan, China.
Mol Oncol. 2018 May;12(5):648-658. doi: 10.1002/1878-0261.12188. Epub 2018 Mar 25.
Lung cancer is the first leading cause of cancer deaths worldwide. Non-small cell lung cancer (NSCLC) is the most common type of lung cancer. Increasing evidence shows that long noncoding RNA (lncRNA) are capable of modulating tumor initiation, proliferation and metastasis. In the present study, we aimed to evaluate whether circulating lncRNA could be used as biomarkers for diagnosis and prognosis of NSCLC. Expression profiles of 14 lncRNA selected from other studies were validated in 20 pairs of tissues by quantitative real-time PCR, and the dysregulated lncRNA thus identified were further validated in serum samples from two independent cohorts along with three tumor makers (CEA, CYFRA21-1, and SCCA). Receiver-operating characteristic analysis was utilized to estimate the diagnostic efficiency of the candidate lncRNA and tumor markers. Importantly, we observed an association between lncRNA expression and overall survival (OS) rate of NSCLC. The expressions of SOX2 overlapping transcript (SOX2OT) and ANRIL were obviously upregulated in NSCLC tissues and serum samples compared with normal controls (P < 0.01). Based on the data from the training set, we next used a logistic regression model to construct an NSCLC diagnostic panel consisting of two lncRNA and three tumor markers. The area under the curve of this panel was 0.853 (95% confidence interval = 0.804-0.894, sensitivity = 77.1%, specificity = 79.2%), and this was distinctly superior to any biomarker alone (all at P < 0.05). Similar results were observed in the validation set. Intriguingly, Kaplan-Meier analysis demonstrated that low expressions of SOX2OT and ANRIL were both associated with higher OS rate (P = 0.008 and 0.017, respectively), and SOX2OT could be used as an independent prognostic factor (P = 0.036). Taken together, our study demonstrated that the newly developed diagnostic panel consisting of SOX2OT, ANRIL, CEA, CYFRA21-1, and SCCA could be valuable in NSCLC diagnosis. LncRNA SOX2OT and ANRIL might be ideal biomarkers for NSCLC prognosis.
肺癌是全球癌症死亡的首要原因。非小细胞肺癌(NSCLC)是最常见的肺癌类型。越来越多的证据表明,长链非编码 RNA(lncRNA)能够调节肿瘤的发生、增殖和转移。在本研究中,我们旨在评估循环 lncRNA 是否可作为 NSCLC 诊断和预后的生物标志物。通过定量实时 PCR 验证了从其他研究中选择的 14 种 lncRNA 的表达谱,在两个独立队列的血清样本中进一步验证了由此确定的失调 lncRNA,以及三个肿瘤标志物(CEA、CYFRA21-1 和 SCCA)。接收者操作特征分析用于估计候选 lncRNA 和肿瘤标志物的诊断效率。重要的是,我们观察到 lncRNA 表达与 NSCLC 总生存率(OS)之间存在关联。SOX2 重叠转录物(SOX2OT)和 ANRIL 在 NSCLC 组织和血清样本中的表达明显高于正常对照组(P<0.01)。基于训练集的数据,我们接下来使用逻辑回归模型构建了一个由两个 lncRNA 和三个肿瘤标志物组成的 NSCLC 诊断面板。该面板的曲线下面积为 0.853(95%置信区间= 0.804-0.894,灵敏度= 77.1%,特异性= 79.2%),明显优于任何单一标志物(均为 P<0.05)。在验证集中也观察到了类似的结果。有趣的是,Kaplan-Meier 分析表明,SOX2OT 和 ANRIL 的低表达均与更高的 OS 率相关(P=0.008 和 0.017),SOX2OT 可作为独立的预后因素(P=0.036)。总之,我们的研究表明,由 SOX2OT、ANRIL、CEA、CYFRA21-1 和 SCCA 组成的新诊断面板可用于 NSCLC 的诊断。lncRNA SOX2OT 和 ANRIL 可能是 NSCLC 预后的理想生物标志物。