首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Circulating CUDR, LSINCT-5 and PTENP1 long noncoding RNAs in sera distinguish patients with gastric cancer from healthy controls
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Circulating CUDR, LSINCT-5 and PTENP1 long noncoding RNAs in sera distinguish patients with gastric cancer from healthy controls

机译:血清中循环的CUDR,LSINCT-5和PTENP1长非编码RNA将胃癌患者与健康对照区分开来

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摘要

The examination of circulating nucleic acids (CNAs) is an emerging noninvasive diagnostic technique. However, it is unclear if serum long noncoding RNAs (lncRNAs) represent a novel marker to detect gastric cancer (GC). In this study, we measured 39 candidate cancer-associated lncRNAs by reverse transcription and quantitative polymerase chain reaction (RT-qPCR) in sera from 110 patients with GC, 106 age- and sex-matched healthy subjects and 15 patients with gastric peptic ulcer, markers were validated and assessed by RT-qPCR. The correlation of the expression levels of the candidate serum lncRNAs with clinical parameters of GC patients was performed. A three-lncRNA signature, including CUDR, LSINCT-5 and PTENP1, was identified that may be potential diagnostic marker for GC. The areas under the receiver operating characteristic (ROC) curve for this serum three-lncRNA signature were 0.920 and 0.829 for the two sets of serum samples. Moreover, a risk model for the serum three-lncRNA signature demonstrated that healthy samples can be distinguished from early GC samples. Three-lncRNA signature in serum was identified as diagnostic marker for GC. This work may facilitate the detection of GC and serve as the basis for further studies of the clinical value of serum lncRNAs in maintaining surveillance and forecasting prognosis.
机译:循环核酸(CNA)的检查是一种新兴的无创诊断技术。但是,尚不清楚血清长非编码RNA(lncRNA)是否代表检测胃癌(GC)的新标记。在这项研究中,我们通过逆转录和定量聚合酶链反应(RT-qPCR)在110例GC患者,106例年龄和性别相匹配的健康受试者以及15例胃消化性溃疡患者的血清中测量了39种与癌症相关的lncRNA,通过RT-qPCR验证和评估标记。进行了候选血清lncRNAs表达水平与GC患者临床参数的相关性分析。确定了三个lncRNA签名,包括CUDR,LSINCT-5和PTENP1,它们可能是GC的潜在诊断标记。对于两组血清样品,该血清三-lncRNA信号的接收者工作特征(ROC)曲线下的面积分别为0.920和0.829。此外,血清三lncRNA签名的风险模型表明,健康样品可以与早期GC样品区分开。血清中的三lncRNA特征被鉴定为GC的诊断标记。这项工作可能有助于检测GC,并作为进一步研究血清lncRNA在维持监测和预测预后方面的临床价值的基础。

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