Department of Pediatrics, Yidu Central Hospital of Weifang, Weifang, Shandong, China.
Eur Rev Med Pharmacol Sci. 2018 Sep;22(18):5914-5919. doi: 10.26355/eurrev_201809_15920.
MiRNAs have been considered to participate in many processes of various cancers, including gastric cancer (GC). However, the significance of miRNAs in the progression prognosis of GC is largely unknown. The goal of this study was to determine the expression level of miR-1236-3p in GC and its clinical association.
Clinical specimens from GC patients were obtained to quantify the expression level of miR-1236-3p using quantitative Real-time PCR. The correlation between the miR-1236-3p levels and the clinicopathological factors of the GC patients was analyzed. The association between miR-1236-3p expression and overall survival was estimated by the Kaplan-Meier method. The significance of different variables with respect to survival was analyzed using the univariate and multivariate Cox proportional hazards model.
We found that miR-1236-3p was significantly downregulated in GC tissues compared to non-tumor gastric tissues (p < 0.01). The levels of miR-1236-3p expression were associated significantly with clinical stage (p = 0.002), lymph node metastasis (p = 0.000) and distant metastasis (p = 0.017). Kaplan-Meier survival analysis showed that patients in the high miR-1236-3p expression group had better overall survival than those in the low miR-1236-3p expression group (p = 0.0039). Moreover, we confirmed that miR-1236-3p was an independent poor prognostic factor for GC patients through univariate and multivariate analysis.
Our findings provide evidence that miR-1236-3p expression is frequently decreased in GC tissues, and its low expression may be a significant prognostic factor for poor survival in GC patients.
miRNAs 被认为参与了多种癌症的多个过程,包括胃癌(GC)。然而,miRNAs 在 GC 进展预后中的意义在很大程度上尚不清楚。本研究旨在确定 miR-1236-3p 在 GC 中的表达水平及其临床相关性。
从 GC 患者获得临床标本,使用定量实时 PCR 定量 miR-1236-3p 的表达水平。分析 miR-1236-3p 水平与 GC 患者临床病理因素的相关性。通过 Kaplan-Meier 法估计 miR-1236-3p 表达与总生存期的关系。使用单变量和多变量 Cox 比例风险模型分析不同变量与生存的关系。
我们发现 miR-1236-3p 在 GC 组织中明显下调,与非肿瘤胃组织相比(p < 0.01)。miR-1236-3p 表达水平与临床分期显著相关(p = 0.002),与淋巴结转移(p = 0.000)和远处转移(p = 0.017)显著相关。Kaplan-Meier 生存分析显示,高 miR-1236-3p 表达组患者的总生存期优于低 miR-1236-3p 表达组(p = 0.0039)。此外,我们通过单变量和多变量分析证实,miR-1236-3p 是 GC 患者的独立预后不良因素。
我们的研究结果表明,miR-1236-3p 在 GC 组织中表达频率降低,其低表达可能是 GC 患者生存不良的重要预后因素。