Department of Thoracic Surgery, Chinese PLA General Hospital, Haidian, Beijing, China.
Eur Rev Med Pharmacol Sci. 2017 Oct;21(17):3866-3870.
Long non-coding RNA MIR31HG (MIR31HG) has been shown to affect numerous tumorigenesis. However, the function of MIR31HG in esophageal squamous cell carcinoma (ESCC) remains unclear. The aim of this study was to investigate whether the levels of MIR31HG could be served as a prognostic factor in patients with ESCC.
MIR31HG expression was detected in 185 samples of surgically resected ESCC and matched normal tumor-adjacent tissues by qRT-PCR. The association between MIR31HG expression levels in tissue and characteristics was examined. Overall survival (OS) curves were conducted to compare MIR31HG level and clinical characteristics. Cox regression analysis was conducted to determine the prognostic value of MIR31HG.
The levels of MIR31HG were decreased in the ESCC tissues from patients with ESCC compared with the control (p < 0.01). In malignant cases, lower expression MIR31HG levels were significantly associated with poor differentiation (p < 0.001), advanced lymph node metastasis (p = 0.006), positive distant metastasis (p = 0.005) and TNM stage (p = 0.004). Kaplan-Meier analysis indicated that patients presenting with reduced MIR31HG expression exhibited poorer OS (p = 0.0002). Univariate and multivariate analysis suggested that MIR31HG expression was an independent prognostic marker for survival in patients with ESCC.
We observed that down-regulated MIR31HG in ESCC patients was associated with malignant clinical characteristics. MIR31HG might be considered as a potential prognostic indicator and a potential target for therapeutic targets in ESCC.
长链非编码 RNA MIR31HG(MIR31HG)已被证明影响许多肿瘤发生。然而,MIR31HG 在食管鳞状细胞癌(ESCC)中的功能仍不清楚。本研究旨在探讨 MIR31HG 的水平是否可以作为 ESCC 患者的预后因素。
通过 qRT-PCR 检测 185 例手术切除的 ESCC 及匹配的正常肿瘤旁组织中 MIR31HG 的表达。检查组织中 MIR31HG 表达水平与特征之间的关联。进行总生存(OS)曲线比较 MIR31HG 水平与临床特征。Cox 回归分析确定 MIR31HG 的预后价值。
与对照相比,ESCC 患者的 ESCC 组织中 MIR31HG 的水平降低(p < 0.01)。在恶性病例中,MIR31HG 水平较低的表达与低分化(p < 0.001)、淋巴结转移(p = 0.006)、远处转移阳性(p = 0.005)和 TNM 分期(p = 0.004)显著相关。Kaplan-Meier 分析表明,MIR31HG 表达降低的患者 OS 较差(p = 0.0002)。单因素和多因素分析表明,MIR31HG 表达是 ESCC 患者生存的独立预后标志物。
我们观察到 ESCC 患者下调的 MIR31HG 与恶性临床特征相关。MIR31HG 可能被认为是 ESCC 的潜在预后指标和治疗靶点。