Wang Xuanyi, Huang Yuxiang, Zhuang Haiwen, Qian Yayun, Zhao Qiu, Yang Lin, Gu Hao, Chen Jue, Guo Renhua, Liu Yanqing
Clin Lab. 2015;61(9):1331-6. doi: 10.7754/clin.lab.2015.150319.
The relationship between microRNA-1 (miR-1) expression and prognosis has not been reported in hepatocellular carcinoma (HCC). The present study aimed to explore the clinicopathological significance and the prognostic role of miR-1 in HCC.
The expression levels of miR-1 were quantified using real-time quantitative PCR (q-PCR) in 40 surgically resected HCC samples and matched adjacent non-cancerous tissues.
MiR-1 expression was significantly downregulated in HCC compared with matched non-cancerous tissues. Aberrant miR-1 expression was significantly correlated with gender, expression of hepatitis B virus surface antigen (HBsAg), tumor differentiation, vein invasion, and TNM stage. Patients with low expression of miR-1 had significantly reduced overall survival compared with patients with high expression of miR-1 (p = 0.04).The multivariate Cox regression analysis indicated that miR-1 expression (HR = 2.79; p = 0.005), gender (HR = 0.087; p = 0.005), vein invasion (HR = 0.172; p = 0.007), and TNM stage (HR = 3.421; p = 0.001) were independent prognostic factors for overall survival.
Low miR-1 expression is associated with shortened survival time. MiR-1 may act as a potential prognostic biomarker for HCC patients.
肝细胞癌(HCC)中微小RNA-1(miR-1)表达与预后的关系尚未见报道。本研究旨在探讨miR-1在HCC中的临床病理意义及预后作用。
采用实时定量聚合酶链反应(q-PCR)对40例手术切除的HCC样本及其配对的癌旁非癌组织中miR-1的表达水平进行定量分析。
与配对的非癌组织相比,HCC中miR-1表达显著下调。miR-1异常表达与性别、乙肝表面抗原(HBsAg)表达、肿瘤分化、静脉侵犯及TNM分期显著相关。miR-1低表达患者的总生存期显著低于miR-1高表达患者(p = 0.04)。多因素Cox回归分析表明,miR-1表达(HR = 2.79;p = 0.005)、性别(HR = 0.087;p = 0.005)、静脉侵犯(HR = 0.172;p = 0.007)及TNM分期(HR = 3.421;p = 0.001)是总生存期的独立预后因素。
miR-1低表达与生存时间缩短相关。miR-1可能作为HCC患者潜在的预后生物标志物。