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Identification of circulating microRNA signatures as potential noninvasive biomarkers for prediction and prognosis of lymph node metastasis in gastric cancer

机译:鉴定循环微RNA标记物作为潜在无创生物标志物用于预测和预测胃癌淋巴结转移

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摘要

Circulating microRNAs (miRNAs) are emerging as novel noninvasive biomarkers for prediction of lymph node metastasis (LNM) in cancer. The aim of this study was to identify serum miRNA signatures for prediction and prognosis of LNM in gastric cancer (GC). MiSeq sequencing was performed for an initial screening of serum miRNAs in 10 GC patients with LNM, 10 patients without LNM and 10 healthy controls. Reverse transcription quantitative real-time PCR was applied to confirm concentration of candidate miRNAs using a training cohort (n = 279) and a validation cohort (n = 180). We identified a four-miRNA panel (miR-501-3p, miR-143-3p, miR-451a, miR-146a) by multivariate logistic regression model that provided high predictive accuracy for LNM with an area under the receiver operating characteristic curve (AUC) of 0.891 (95% CI, 0.840 to 0.930) in training set. Prospective evaluation of this panel revealed an AUC of 0.822 (95% CI, 0.758 to 0.875, specificity = 87.78%, sensitivity = 63.33%) in validation set. Moreover, Kaplan–Meier analysis showed that LNM patients with low miR-451a and miR-146a levels had worse overall survival (OS) (p < 0.05). In Cox regression analysis, miR-451a was independently associated with OS of LNM (p = 0.028). Our results suggested that use of serum miRNAs seems promising in estimating the probability GC patients harbor LNM and providing prognostic information for LNM.
机译:循环微RNA(miRNA)逐渐成为预测癌症中淋巴结转移(LNM)的新型非侵入性生物标记。这项研究的目的是确定血清miRNA的特征,以预测和预测胃癌(GC)中LNM。进行MiSeq测序以初步筛查10名患有LNM的GC患者,10名没有LNM的患者和10名健康对照的血清miRNA。使用训练队列(n = 279)和验证队列(n = 180),应用逆转录定量实时PCR来确认候选miRNA的浓度。我们通过多元logistic回归模型确定了四个miRNA面板(miR-501-3p,miR-143-3p,miR-451a,miR-146a),该模型为LNM提供了较高的预测精度,且接收器工作特征曲线下的面积为(训练集中的AUC)为0.891(95%CI,0.840至0.930)。该小组的前瞻性评估显示,验证集中的AUC为0.822(95%CI,0.758至0.875,特异性= 87.78%,灵敏度= 63.33%)。此外,Kaplan–Meier分析显示,miR-451a和miR-146a水平较低的LNM患者的总生存期(OS)较差(p <0.05)。在Cox回归分析中,miR-451a与LNM的OS独立相关(p = 0.028)。我们的结果表明,使用血清miRNA似乎有望估计GC患者携带LNM的可能性并提供LNM的预后信息。

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