Leng Qixin, Lin Yanli, Jiang Fangran, Lee Cheng-Ju, Zhan Min, Fang HongBin, Wang Yue, Jiang Feng
Department of Pathology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Departments of Biological Sciences, University of Maryland, Baltimore County, Baltimore, MD 21250, USA.
Oncotarget. 2017 Dec 5;8(67):111902-111911. doi: 10.18632/oncotarget.22950. eCollection 2017 Dec 19.
The early detection of lung cancer continues to be a major clinical challenge. Using whole-transcriptome next-generation sequencing to analyze lung tumor and the matched noncancerous tissues, we previously identified 54 lung cancer-associated microRNAs (miRNAs). The objective of this study was to investigate whether the miRNAs could be used as plasma biomarkers for lung cancer. We determined expressions of the lung tumor-miRNAs in plasma of a development cohort of 180 subjects by using reverse transcription PCR to develop biomarkers. The development cohort included 92 lung cancer patients and 88 cancer-free smokers. We validated the biomarkers in a validation cohort of 64 individuals comprising 34 lung cancer patients and 30 cancer-free smokers. Of the 54 miRNAs, 30 displayed a significant different expression level in plasma of the lung cancer patients cancer-free controls (all P < 0.05). A plasma miRNA signature (miRs-126, 145, 210, and 205-5p) with the best prediction was developed, producing 91.5% sensitivity and 96.2% specificity for lung cancer detection. Diagnostic performance of the plasma miRNA signature had no association with stage and histological type of lung tumor, and patients' age, sex, and ethnicity (all p > 0.05). The plasma miRNA signature was reproducibly confirmed in the validation cohort. The plasma miRNA signature may provide a blood-based assay for diagnosing lung cancer at the early stage, and thereby reduce the associated mortality and cost.
肺癌的早期检测仍然是一项重大的临床挑战。我们之前利用全转录组下一代测序技术分析肺癌组织及其匹配的非癌组织,鉴定出了54种与肺癌相关的微小RNA(miRNA)。本研究的目的是调查这些miRNA是否可用作肺癌的血浆生物标志物。我们通过逆转录PCR检测了180名受试者组成的发展队列血浆中肺肿瘤miRNA的表达,以开发生物标志物。该发展队列包括92名肺癌患者和88名无癌吸烟者。我们在一个由34名肺癌患者和30名无癌吸烟者组成的64人验证队列中对这些生物标志物进行了验证。在这54种miRNA中,有30种在肺癌患者与无癌对照者的血浆中表现出显著不同的表达水平(所有P<0.05)。我们开发了一种预测效果最佳的血浆miRNA特征(miR-126、145、210和205-5p),对肺癌检测的灵敏度为91.5%,特异性为96.2%。血浆miRNA特征的诊断性能与肺肿瘤的分期、组织学类型以及患者的年龄、性别和种族均无关联(所有p>0.05)。血浆miRNA特征在验证队列中得到了可重复性确认。血浆miRNA特征可能为早期诊断肺癌提供一种基于血液的检测方法,从而降低相关死亡率和成本。