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Diagnostic Value of Serum miR-182 miR-183 miR-210 and miR-126 Levels in Patients with Early-Stage Non-Small Cell Lung Cancer

机译:血清miR-182miR-183miR-210和miR-126水平对早期非小细胞肺癌的诊断价值

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摘要

Blood-circulating miRNAs could be useful as a biomarker to detect lung cancer early. We investigated the serum levels of four different miRNAs in patients with non-small cell lung cancer (NSCLC) and assessed their diagnostic value for NSCLC. Serum samples from 112 NSCLC patients and 104 controls (20 current smokers without lung cancer, 23 pneumonia patients, 21 gastric cancer patients, and 40 healthy controls) were subjected to Taqman probe-based quantitative reverse transcription–polymerase chain reaction (RT-PCR). The data showed that the serum levels of miR-182, miR-183, and miR-210 were significantly upregulated and that the miR-126 level was significantly downregulated in NSCLC patients, compared with the healthy controls. Further receiver operating characteristic (ROC) curve analysis revealed that the serum miR-182, miR-183, miR-210, or miR-126 level could serve as a diagnostic biomarker for NSCLC early detection, with a high sensitivity and specificity. The combination of these four miRNAs with carcinoembryonic antigen (CEA) further increased the diagnostic value, with an area under the curve (AUC) of 0.965 (sensitivity, 81.3%; specificity, 100.0%; and accuracy, 90.8%) using logistic regression model analysis. In addition, the relative levels of serum miR-182, miR-183, miR-210, and miR-126 could distinguish NSCLC or early-stage NSCLC from current tobacco smokers without lung cancer and pneumonia or gastric cancer patients with a high sensitivity and specificity. Data from the current study validated that the four serum miRNAs could serve as a tumor biomarker for NSCLC early diagnosis.
机译:血液循环的miRNA可用作早期检测肺癌的生物标志物。我们调查了非小细胞肺癌(NSCLC)患者的四种不同miRNA的血清水平,并评估了其对NSCLC的诊断价值。对来自112例NSCLC患者和104例对照(20名目前没有肺癌的吸烟者,23例肺炎患者,21例胃癌患者和40名健康对照)的血清样本进行了基于Taqman探针的定量逆转录聚合酶链反应(RT-PCR) 。数据显示,与健康对照组相比,NSCLC患者的miR-182,miR-183和miR-210的血清水平显着上调,而miR-126的水平显着下调。进一步的受试者工作特征(ROC)曲线分析表明,血清miR-182,miR-183,miR-210或miR-126水平可以作为NSCLC早期检测的诊断生物标志物,具有很高的灵敏度和特异性。这四种miRNA与癌胚抗原(CEA)的组合进一步提高了诊断价值,使用逻辑回归模型,曲线下面积(AUC)为0.965(灵敏度为81.3%;特异性为100.0%;准确性为90.8%)。分析。此外,血清miR-182,miR-183,miR-210和miR-126的相对水平可以将NSCLC或早期NSCLC与目前没有肺癌,肺炎或胃癌的吸烟者高度区分,并且特异性。来自当前研究的数据证实了这四种血清miRNA可以作为NSCLC早期诊断的肿瘤生物标志物。

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