Hui Beina, Chen Xin, Hui Lingyun, Xi Ruxing, Zhang Xiaozhi
Department of Radiation Oncology, First Affiliated Hospital of Xi'an Jiaotong University School of Medicine, Xi'an, Shaanxi 710061, P.R. China.
Department of Clinical Laboratory, First Affiliated Hospital of Xi'an Jiaotong University School of Medicine, Xi'an, Shaanxi 710061, P.R. China.
Oncol Lett. 2015 Nov;10(5):3008-3012. doi: 10.3892/ol.2015.3642. Epub 2015 Aug 25.
The aim of the present study was to investigate the feasibility and value of serum microRNAs (miRNAs/miRs) as biological markers for the prediction of the behavior and prognosis of esophageal squamous cell cancer (ESCC). The differential expression of serum miRNA was detected by an miRNA microarray of 9 patients with ESCC and 9 healthy volunteers. The result of the miRNA microarray was validated in serum samples of 69 patients with ESCC and 14 healthy volunteers by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The association between serum miRNA expression and tumor-node-metastasis (TNM) stage was analyzed. A total of 10 serum-specific miRNAs were identified from the patients with ESCC. Through PCR verification, the expression levels of miR-129, miR-451 and miR-365 were consistent with the microarray results validated by RT-qPCR, and the difference was statistically significant compared with the healthy volunteers (P=0.007, P=0.007 and P<0.001, respectively). Multivariate logistic regression analysis showed that miR-365 could serve as potential diagnostic marker for ESCC; the area under the receiver operating characteristic curve was 0.831, with a sensitivity of 80.56% and a specificity of 86.7%, but its expression did not differ significantly among the different TNM stages (stage I-II vs. III, P=0.052; stage III vs. IV, P=0.069). The expression level of miRNA-129 differed significantly among the different stages (stage I-II vs. III, P=0.002; stage III vs. IV, P=0.042), while the expression level of miR-451 did not differ significantly between stage III and IV (P=0.308). In conclusion, serum microRNAs are novel biomarkers for ESCC, and miRNA-365 and miRNA-129 can be used for the early prediction of cancer and the prediction of clinical stage, respectively.
本研究的目的是探讨血清微小RNA(miRNA/miR)作为预测食管鳞状细胞癌(ESCC)行为和预后的生物标志物的可行性和价值。通过对9例ESCC患者和9名健康志愿者进行miRNA微阵列检测血清miRNA的差异表达。通过逆转录定量聚合酶链反应(RT-qPCR)在69例ESCC患者和14名健康志愿者的血清样本中验证了miRNA微阵列的结果。分析了血清miRNA表达与肿瘤-淋巴结-转移(TNM)分期之间的关联。从ESCC患者中总共鉴定出10种血清特异性miRNA。通过PCR验证,miR-129、miR-451和miR-365的表达水平与RT-qPCR验证的微阵列结果一致,与健康志愿者相比差异具有统计学意义(分别为P=0.007、P=0.007和P<0.001)。多因素逻辑回归分析表明,miR-365可作为ESCC的潜在诊断标志物;受试者工作特征曲线下面积为0.831,灵敏度为80.56%,特异性为86.7%,但其在不同TNM分期之间的表达差异无统计学意义(I-II期与III期,P=0.052;III期与IV期,P=0.069)。miRNA-129的表达水平在不同分期之间差异有统计学意义(I-II期与III期,P=0.002;III期与IV期,P=0.042),而miR-451在III期和IV期之间的表达水平差异无统计学意义(P=0.308)。总之,血清微小RNA是ESCC的新型生物标志物,miRNA-365和miRNA-129可分别用于癌症的早期预测和临床分期的预测。