He Rong-Quan, Huang Zhi-Guang, Li Tian-Yu, Wei Yan-Ping, Chen Gang, Lin Xing-Gu, Wang Qiu-Yan
Department of Biochemistry and Molecular Biology, Guangxi Medical University, Nanning,
Center for Genomic and Personalized Medicine, Nanning,
Cell Physiol Biochem. 2018;50(4):1474-1495. doi: 10.1159/000494647. Epub 2018 Oct 25.
BACKGROUND/AIMS: Current practical advances in high-throughput data technologies including RNA-sequencing have led to the identification of long non-coding RNAs (lncRNAs) for potential clinical application against bladder urothelial cancer (BLCA). However, most previous studies focused on the clinical value of individual lncRNAs, which has limited the potential for future clinical application.
In this study, RNA-sequencing data of lncRNAs was downloaded from The Cancer Genome Atlas database. Risk score was constructed based on survival-associated lncRNAs identified using differential expression analysis as well as univariate and multivariate Cox proportional hazards regression analysis. Receiver operating characteristic and Kaplan-Meier curve analyses were employed to evaluate the clinical and prognostic value of risk scores. Bioinformatics analyses were used to investigate the potential mechanisms of newly identified lncRNAs.
Among 2,127 differentially expressed lncRNAs (DELs), four new lncRNAs (AC145124.1, AC010168.2, MIR200CHG, and AC098613.1) showed valuable prognostic effects in BLCA patients. More importantly, the four-DEL-based risk score had the potential to become an independent marker for the survival status prediction of BLCA patients. Distinct co-expressed genes and signaling pathways were identified when BLCA was categorized into low- and high-risk groups. Furthermore, a protein-coding gene, HIST4H4 was found only 68 bp from the AC010168.2 DEL. HIST4H4 expression level was evidently up-regulated and positively correlated with AC010168.2 in BLCA patients.
This in silico investigation pioneers the future investigation of the utility of prognostic lncRNAs for BLCA.
背景/目的:包括RNA测序在内的高通量数据技术目前的实际进展已促使人们鉴定出长链非编码RNA(lncRNA),用于膀胱癌(BLCA)的潜在临床应用。然而,以往大多数研究都集中在单个lncRNA的临床价值上,这限制了其未来临床应用的潜力。
在本研究中,从癌症基因组图谱数据库下载lncRNA的RNA测序数据。基于使用差异表达分析以及单变量和多变量Cox比例风险回归分析鉴定出的与生存相关的lncRNA构建风险评分。采用受试者工作特征曲线和Kaplan-Meier曲线分析来评估风险评分的临床和预后价值。利用生物信息学分析来研究新鉴定出的lncRNA的潜在机制。
在2127个差异表达的lncRNA(DEL)中,四种新的lncRNA(AC145124.1、AC010168.2、MIR200CHG和AC098613.1)在BLCA患者中显示出有价值的预后作用。更重要的是基于这四种DEL的风险评分有可能成为预测BLCA患者生存状态的独立标志物。当将BLCA分为低风险和高风险组时,鉴定出了不同的共表达基因和信号通路。此外,发现一个蛋白质编码基因HIST4H4距离DEL AC010168.2仅68 bp。在BLCA患者中,HIST4H4的表达水平明显上调且与AC010168.2呈正相关关系。
这项计算机模拟研究开创了对BLCA预后lncRNA效用未来研究的先河。