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运用深度测序技术鉴定与鼻咽癌相关的潜在长链非编码RNA

Identification of potential long noncoding RNA associated with nasopharyngeal carcinoma using deep sequencing.

作者信息

Xu Yu-Zhong, Chen Fang-Fang, Zhang Yu, Liang Hui, Li Xiao-Jun, He Chen

机构信息

1 Department of Clinical Laboratory Science, Shenzhen Baoan Hospital, Southern Medical University, Shenzhen, China.

2 Department of Clinical Laboratory Science, Jinling Hospital, Southern Medical University, Nanjing, Jiangsu province, China.

出版信息

J Int Med Res. 2019 Jul;47(7):3271-3281. doi: 10.1177/0300060519845973. Epub 2019 May 24.

Abstract

OBJECTIVE

To identify differentially expressed long noncoding RNAs (lncRNAs) in nasopharyngeal carcinoma (NPC) compared with chronic nasopharyngitis (CNP) tissues.

METHODS

This prospective cohort study enrolled patients with NPC and CNP. The levels of lncRNAs in NPC and CNP tissues was detected by deep sequencing and quantitative polymerase chain reaction. Kyoto Encyclopedia of Genes and Genomes pathway analysis and antisense prediction were performed to reveal the function of differentially expressed lncRNAs (DELs). Receiver operating characteristic (ROC) curve and correlation analyses were used to evaluate the clinical and prognostic value of lncRNAs.

RESULTS

A total of 30 NPC and 27 CNP tissues were analysed. A total of 296 DELs were identified. LncRNAs ENSG00000227084 and ENSG00000230489 might play important roles in the development of NPC by interfering with the Rap1 signalling pathway and natural killer cell-mediated cytotoxicity, respectively. Antisense prediction showed that lncRNA ENSG00000230489 was paired with VAV3 mRNA. LncRNAs ENSG00000230489 (area under the ROC curve = 0.9138) and ENSG00000227084 (area under the ROC curve = 0.8037) may be diagnostic markers for NPC. Furthermore, low levels of ENSG00000230489 was positively associated with distant metastasis.

CONCLUSION

LncRNAs ENSG00000230489 and ENSG00000227084 may be potential diagnostic markers and therapeutic targets for NPC.

摘要

目的

鉴定与慢性鼻咽炎(CNP)组织相比,鼻咽癌(NPC)中差异表达的长链非编码RNA(lncRNA)。

方法

这项前瞻性队列研究纳入了NPC和CNP患者。通过深度测序和定量聚合酶链反应检测NPC和CNP组织中lncRNA的水平。进行京都基因与基因组百科全书通路分析和反义预测以揭示差异表达lncRNA(DEL)的功能。采用受试者工作特征(ROC)曲线和相关性分析来评估lncRNA的临床和预后价值。

结果

共分析了30例NPC组织和27例CNP组织。共鉴定出296个DEL。lncRNA ENSG00000227084和ENSG00000230489可能分别通过干扰Rap1信号通路和自然杀伤细胞介导的细胞毒性在NPC的发生发展中发挥重要作用。反义预测显示lncRNA ENSG00000230489与VAV3 mRNA配对。lncRNA ENSG00000230489(ROC曲线下面积=0.9138)和ENSG00000227084(ROC曲线下面积=0.8037)可能是NPC的诊断标志物。此外,ENSG00000230489低水平与远处转移呈正相关。

结论

lncRNA ENSG00000230489和ENSG00000227084可能是NPC潜在的诊断标志物和治疗靶点。

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