Department of Biomedical Sciences, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand.
Department of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand.
Cancer Biol Med. 2020 Aug 15;17(3):652-663. doi: 10.20892/j.issn.2095-3941.2020.0063.
: MicroRNA (miRNA), a short noncoding RNA, is claimed to be a potential blood-based biomarker. We aimed to identify and evaluate miRNAs as diagnostic biomarkers for non-small cell lung cancer (NSCLC). : Profiles of 745 miRNAs were screened in the serum of 8 patients with NSCLC and 8 age- and sex-matched controls using TaqMan low-density arrays (TLDAs) and validated in 25 patients with NSCLC and 30 with other lung diseases (OLs) as well as in 19 healthy persons (HPs). The diagnostic performance of the candidate miRNAs was assessed in 117 cases of NSCLC and 113 OLs using quantitative real-time polymerase chain reaction (qRT-PCR). Differences in miRNA expression between patients with NSCLC and controls were assessed using the Mann-Whitney U test. The area under receiver operating characteristic (ROC) curve (AUC) was obtained based on the logistic regression model. : Ten miRNAs were found to be differentially expressed between patients with NSCLC and controls, including miR-769, miR-339-3p, miR-339-5p, miR-519a, miR-1238, miR-99a#, miR-134, miR-604, miR-539, and miR-342. The expression of miR-339-3p was significantly higher in patients with NSCLC than in those with OLs ( < 0.001) and HPs ( = 0.020). ROC analysis revealed an miR-339-3p expression AUC of 0.616 [95% confidence interval (CI): 0.561-0.702]. The diagnostic prediction was increased (AUC = 0.706, 95% CI: 0.649-0.779) in the model combining miR-339-3p expression and other known risk factors (i.e., age, smoking status, and drinking status). : MiR-339-3p was significantly upregulated in patients with NSCLC compared with participants without cancer, suggesting a diagnostic prediction value for high-risk individuals. Therefore, miR-339-3p expression could be a potential blood-based biomarker for NSCLC.
: 微小 RNA(miRNA)是一种短的非编码 RNA,据称是一种有潜力的基于血液的生物标志物。我们旨在鉴定和评估 miRNA 作为非小细胞肺癌(NSCLC)的诊断生物标志物。: 使用 TaqMan 低密度阵列(TLDAs)在 8 例 NSCLC 患者和 8 例年龄和性别匹配的对照者的血清中筛选了 745 种 miRNA 表达谱,并在 25 例 NSCLC 患者、30 例其他肺部疾病(OLs)患者和 19 例健康者(HPs)中进行了验证。使用定量实时聚合酶链反应(qRT-PCR)在 117 例 NSCLC 病例和 113 例 OL 病例中评估候选 miRNA 的诊断性能。使用 Mann-Whitney U 检验评估 NSCLC 患者和对照组之间 miRNA 表达的差异。基于逻辑回归模型获得接收器工作特征(ROC)曲线下面积(AUC)。: 发现 10 种 miRNA 在 NSCLC 患者和对照组之间存在差异表达,包括 miR-769、miR-339-3p、miR-339-5p、miR-519a、miR-1238、miR-99a#、miR-134、miR-604、miR-539 和 miR-342。miR-339-3p 在 NSCLC 患者中的表达明显高于 OLs 患者(<0.001)和 HPs(=0.020)。ROC 分析显示 miR-339-3p 表达 AUC 为 0.616 [95%置信区间(CI):0.561-0.702]。在结合 miR-339-3p 表达和其他已知危险因素(即年龄、吸烟状况和饮酒状况)的模型中,诊断预测值增加(AUC=0.706,95%CI:0.649-0.779)。: 与无癌症参与者相比,miR-339-3p 在 NSCLC 患者中显著上调,表明其对高危个体具有诊断预测价值。因此,miR-339-3p 表达可能是 NSCLC 的一种潜在的基于血液的生物标志物。