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Circulating long noncoding RNA act as potential novel biomarkers for diagnosis and prognosis of non‐small cell lung cancer

机译:循环长的非编码RNA作为非小细胞肺癌诊断和预后的潜在新生物标志物

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摘要

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.
机译:肺癌是全球癌症死亡的第一大主要原因。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,长的非编码RNA(lncRNA)能够调节肿瘤的发生,增殖和转移。在本研究中,我们旨在评估循环中的lncRNA是否可以用作诊断和预后NSCLC的生物标志物。通过定量实时PCR在20对组织中验证了从其他研究中选择的14个lncRNA的表达谱,并在两个独立队列以及三个肿瘤发生者(CEA,CYFRA21-1)的血清样品中进一步验证了由此鉴定出的失调的lncRNA。 ,以及SCCA)。接受者操作特征分析被用来估计候选lncRNA和肿瘤标志物的诊断效率。重要的是,我们观察到了lncRNA表达与NSCLC总体生存率之间的关联。与正常对照组相比,NSCLC组织和血清样品中SOX2重叠转录本(SOX2OT)和ANRIL的表达明显上调(P <0.01)。根据训练集中的数据,我们接下来使用逻辑回归模型构建由两个lncRNA和三个肿瘤标志物组成的NSCLC诊断面板。该面板曲线下的面积为0.853(95%置信区间= 0.804-0.894,灵敏度= 77.1%,特异性= 79.2%),这明显优于单独的任何生物标志物(均在P <0.05)。在验证集中观察到相似的结果。有趣的是,Kaplan-Meier分析表明SOX2OT和ANRIL的低表达均与较高的OS率相关(分别为P = 0.008和0.017),并且SOX2OT可以用作独立的预后因素(P = 0.036)。综上所述,我们的研究表明,由SOX2OT,ANRIL,CEA,CYFRA21-1和SCCA组成的新开发的诊断专家组在NSCLC诊断中可能有价值。 LncRNA SOX2OT和ANRIL可能是NSCLC预后的理想生物标志物。

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