Wang Cheng, Hu Jicheng, Lu Meiling, Gu Hongwei, Zhou Xiaojun, Chen Xi, Zen Ke, Zhang Chen-Yu, Zhang Tiehui, Ge Jingping, Wang Junjun, Zhang Chunni
1] Department of Clinical Laboratory, Jinling Hospital, School of Life Sciences, Nanjing University, Nanjing 210002, China [2] Jiangsu Engineering Research Center for microRNA Biology and Biotechnology, State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, China.
Department of Urology, The Fifth Affiliated Hospital of Harbin Medical University, Daqing, China.
Sci Rep. 2015 Jan 5;5:7610. doi: 10.1038/srep07610.
Circulating microRNAs (miRNAs) are emerging as clinically useful tools for cancer detection; however, little is known about their early diagnostic impact on RCC. The levels of 754 serum miRNAs were initially determined using a TaqMan Low Density Array in two pooled samples from 25 RCC and 25 noncancer controls. Markedly dysregulated miRNAs in RCC cases were subsequently validated individually by qRT-PCR in another 107 patients and 107 controls arranged in two sets. The serum levels of miR-193a-3p, miR-362 and miR-572 were significantly increased whereas the levels of miR-28-5p and miR-378 were markedly decreased in patients with RCC, even in those with stage I disease, compared with the noncancer controls (P < 0.01). The areas under the ROC curve (AUCs) for the 5 combined miRNAs were 0.807 (95% CI, 0.687-0.928) and 0.796 (95% CI, 0.724-0.867) for the training set and the validation set, respectively. Furthermore, the panel enabled the differentiation of stage I RCC from controls with AUC of 0.807 (95% CI, 0.731-0.871), a sensitivity of 80% and a specificity of 71%. This panel of 5 serum miRNA may have the potential to be used clinically as an auxiliary diagnostic tool for the early detection of RCC.
循环微RNA(miRNA)正逐渐成为癌症检测中具有临床应用价值的工具;然而,关于它们对肾细胞癌(RCC)的早期诊断作用却知之甚少。最初使用TaqMan低密度阵列在来自25例RCC患者和25例非癌症对照的两个混合样本中测定了754种血清miRNA的水平。随后,在另外107例患者和107例对照(分为两组)中通过qRT-PCR对RCC病例中明显失调的miRNA进行了单独验证。与非癌症对照相比,RCC患者中miR-193a-3p、miR-362和miR-572的血清水平显著升高,而miR-28-5p和miR-378的水平则显著降低,即使是I期疾病患者也是如此(P < 0.01)。5种组合miRNA的ROC曲线下面积(AUC)在训练集和验证集中分别为0.807(95%CI,0.687 - 0.928)和0.796(95%CI,0.724 - 0.867)。此外,该检测组合能够将I期RCC与对照区分开来,AUC为0.807(95%CI,0.731 - 0.871),灵敏度为80%,特异性为71%。这一包含5种血清miRNA的检测组合可能有潜力在临床上用作RCC早期检测的辅助诊断工具。