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首页> 外文期刊>BMC Cancer >Serum miRNAs, a potential prognosis marker of loco-regionally advanced nasopharyngeal carcinoma patients treated with CCRT
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Serum miRNAs, a potential prognosis marker of loco-regionally advanced nasopharyngeal carcinoma patients treated with CCRT

机译:血清miRNA,潜在预后标志物的基因群教晚期鼻咽癌患者治疗CCRT

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BACKGROUND:Serum miRNA was once found as potential disease survival index,thus we investigated the role of miRNA in predicting prognosis in loco-regionally advanced NPC patients treated with CCRT.METHODS:This study included two phases: (i) We enrolled 3 NPC patients with recurrence or distant metastasis (experimental group, EG) and 3 NPC patients in clinical remission (control group, CG),who were treated with CCRT within 5?years. The paired serum was collected before and after treatment and biomarkers were discovered by LNA-TaqMan Human MicroRNA Arrays. (ii) we used the bioinformatic analysis, marker selection and an independent validation by qRT-PCR to analyse the serums of 29 NPC patients with recurrent disease or distant metastasis and 19 NPC patients in clinical remission treated with CCRT. Using the Kaplan-Meier method, log-rank test and Cox regression model to estimate the accuracy of the miRNAs to predict PFS and OS, and identified factors significantly associated with prognosis, respectively.RESULTS:Using fold change≥2.0 or?≤?0.5 and p?≤?0.05 as cutoff levels, we identified 1 up-regulated and 6 down-regulated miRNAs, 1 up-regulated and 9 down-regulated miRNAs in EG versus CG before and after CCRT, respectively. After these down-regulated miRNAs were dealed with bioinformatics analysis and normalization, only 5 different miRNAs were significantly reduced, which there were no significant difference in the expression of miRNA-26b, miRNA-29a and miRNA-125b before CCRT, and the expression of miRNA-143 and miRNA-29b after CCRT in the serum samples of 48 NPC patients. Based on this, we calculated a risk score with the expression of miRNA-26b、miRNA-29a、miRNA-125b、miRNA-29b、miRNA-143 and then classified patients as high or low risk group. Cox regression model suggested that combining miRNA-29a and miRNA-125b before CCRT with miRNA-26b after CCRT was independent prognostic factors for PFS (HR?=?3.149, 95%CI:1.018-9.115, p?=?0.034), whereas combining the former two is independent for OS (HR?=?5.146, 95%CI:1.674-15.817, p?=?0.04).CONCLUSIONS:For loco-regionally advanced NPC patients treated with CCRT, especially high-risk patients- serum miRNAs, such as miRNA-29a, miRNA-125b and miRNA-26b etc., play an important role in predicting prognosis factors of PFS and OS, which will contribute to the strategic direction for future research.
机译:背景:血清miRNA曾被发现作为潜在的疾病存活指数,因此我们研究了miRNA在预测CCRT中治疗的基因区域晚期NPC患者中预测预后的作用:本研究包括两种阶段:(i)我们注册了3名NPC患者随着临床缓解(对照组,CG)的复发或远处转移(实验组,例如)和3名NPC患者,他在5年内患有CCRT。在治疗之前和之后收集配对的血清,并通过LNA-Taqman人微小阵列发现生物标志物。 (ii)我们使用了QRT-PCR的生物信息分析,标记选择和独立验证,分析29个NPC患者的复发性疾病或远程转移和19个NPC患者,临床缓解患者用CCRT处理。使用Kaplan-Meier方法,日志秩测试和Cox回归模型来估计miRNA的准确性,以预测PFS和OS,分别确定与预后显着相关的因素。结果:使用折叠变化≥2.0或?≤≤0.5并且p?≤α.05作为截止水平,我们在CCRT之前和之后分别鉴定了1个上调和6个下调的miRNA,1个上调和9个下调的miRNA。在将这些下调的miRNA涉及生物信息学分析和归一化之后,只有5种不同的miRNA显着降低,其中MiRNA-26b,miRNA-29a和miRNA-125b的表达没有显着差异,并且在ccrt之前的表达和表达在48个NPC患者的血清样品中CCRT后MiRNA-143和miRNA-29b。基于此,我们计算了MiRNA-26b,miRNA-29a,miRNA-125b,miRNA-29b,miRNA-143,然后分类患者作为高或低风险组的风险评分。 Cox回归模型表明,CCRT后CCRNA-26b与miRNA-26b之前的miRNA-29a和miRNA-125b与PFS独立的预后因子组合(HR?= 3.149,95%CI:1.018-9.115,P?= 0.034),而且结合前两者是独立的OS(HR?= 5.146,95%CI:1.674-15.817,P?= 0.04)。结论:对于患有CCRT,特别是高危患者的基因区域晚期NPC患者 - 血清miRNA,如miRNA-29a,miRNA-125b和miRNA-26b等,在预测PFS和OS的预后因素方面发挥着重要作用,这将有助于未来研究的战略方向。

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