He Baoyu, Zeng Jianchao, Chao Wei, Chen Xiaoli, Huang Yujie, Deng Kaifeng, Huang Zhizhuo, Li Jinwan, Dai Meiyu, Chen Shaojun, Huang Haixin, Dai Shengming
Medical Science Laboratory, The Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi 545005, China.
Department of Oncology, The Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi 545005, China.
Oncotarget. 2017 Jun 20;8(25):41166-41177. doi: 10.18632/oncotarget.17083.
Circulating RNAs in serum, plasma or other body liquid have emerged as useful and highly promising biomarkers for noninvasive diagnostic application. Herein, we aimed to establish a serum long non-coding RNAs (lncRNAs) signature for diagnosing nasopharyngeal carcinoma (NPC). In this study, we recruited a cohort of 101 NPC patients, 20 patients with chronic nasopharyngitis (CN), 20 EBV carriers (EC) and 101 healthy controls. qRT-PCR was performed with NPC cells and serum samples to screen a pool of 38 NPC-related lncRNAs obtained from the LncRNADisease database. A profile of three circulating lncRNAs (MALAT1, AFAP1-AS1 and AL359062) was established for NPC diagnosis. By Receiver Operating Characteristic (ROC) curve analysis, this three-lncRNA signature showed high accuracy in discriminating NPC from healthy controls (AUC = 0.918), CN (AUC = 0.893) or EC (AUC = 0.877). Furthermore, high levels of these three lncRNAs were closely related to advanced NPC tumor node metastasis stages and EBV infection. Serum levels of these three lncRNAs declined significantly in patients after therapy. Our present study indicates that circulating MALAT1, AFAP1-AS1 and AL359062 may represent novel serum biomarkers for NPC diagnosis and prognostic prediction after treatment.
血清、血浆或其他体液中的循环RNA已成为用于无创诊断的有用且极具前景的生物标志物。在此,我们旨在建立一种用于诊断鼻咽癌(NPC)的血清长链非编码RNA(lncRNA)特征。在本研究中,我们招募了101例NPC患者、20例慢性鼻咽炎(CN)患者、20例EB病毒携带者(EC)和101例健康对照。对NPC细胞和血清样本进行qRT-PCR,以筛选从LncRNADisease数据库获得的38种与NPC相关的lncRNA。建立了用于NPC诊断的三种循环lncRNA(MALAT1、AFAP1-AS1和AL359062)特征。通过受试者工作特征(ROC)曲线分析,这种三lncRNA特征在区分NPC与健康对照(AUC = 0.918)、CN(AUC = 0.893)或EC(AUC = 0.877)方面显示出高准确性。此外,这三种lncRNA的高水平与晚期NPC肿瘤淋巴结转移分期和EB病毒感染密切相关。治疗后患者血清中这三种lncRNA的水平显著下降。我们目前的研究表明,循环中的MALAT1、AFAP1-AS1和AL359062可能代表用于NPC诊断和治疗后预后预测的新型血清生物标志物。