Circulating Epstein-Barr virus microRNA profile reveals novel biomarker for nasopharyngeal carcinoma diagnosis

被引:18
|
作者
Wu, Lirong [1 ]
Wang, Jingyi [2 ]
Zhu, Danxia [3 ]
Zhang, Shiyu [4 ]
Zhou, Xin [4 ]
Zhu, Wei [4 ]
Zhu, Jun [1 ]
He, Xia [1 ]
机构
[1] Nanjing Med Univ, Jiangsu Canc Hosp, Jiangsu Inst Canc Res, Dept Radiat Oncol,Affiliated Canc Hosp, 42 Baiziting Rd, Nanjing 210009, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Dept Breast Surg, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
[3] Soochow Univ, Dept Oncol, Affiliated Hosp 3, Changzhou, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Dept Oncol, Affiliated Hosp 1, Nanjing 210000, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Nasopharyngeal carcinoma; Epstein-Barr virus; circulating microRNAs; biomarker; diagnosis; POTENTIAL BIOMARKERS; ENCODED MICRORNAS; EBV DNA; GENE; PLASMA; CANCER; RISK; ACTIVATION; EXPRESSION; PROMOTER;
D O I
10.3233/CBM-190160
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Nasopharyngeal carcinoma (NPC), a tumor quite prevalent in Asia, is closely associated with Epstein-Barr virus (EBV) infection status. Many NPC patients are not able to be treated in time when being diagnosed at an advanced stage. EBV-encoded microRNAs are reliable sources of biomarkers for NPC diagnosis. In this study, we conducted circulating EBV microRNAs profiling by quantitative reverse transcription polymerase chain reaction (qRT-PCR) among plasma samples of 159 NPC patients versus 145 normal controls (NCs) and serum samples of 60 NPC patients versus 60 NCs. Among the 44 mature EBV-encoded miRNAs, only miR-BART19-3p in plasma was proved to be significantly up-regulated in NPC patients (P < 0.05; fold change (FC) > 2.0). The area under the receiver operating characteristic curve (AUC) for the signature to discriminate NPC patients from NCs was 0.848 with the sensitivity and specificity being 71.7% and 72.3%, respectively. The identified biomarker was analyzed in tissue specimens (44 NPC VS. 32 NCs) and proved to be consistently up-regulated in NPC tumor tissues. Bioinformatics analysis was further conducted to predict the potential targets of miR-BART-19-3p, which provided some hints to its close relationship with NPC development. In conclusion, we identified a novel biomarker - plasma miR-BART19-3p for the detection of NPC.
引用
收藏
页码:365 / 375
页数:11
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