Wang Chunwei, Xiang Hua, Si Huiyuan, Guo Dandan, Sun Mei
Department of Surgery and Infections Diseases, Chinese PLA Air Force General Hospital Beijing 100142, China.
Int J Clin Exp Pathol. 2015 Nov 1;8(11):14818-23. eCollection 2015.
Myofibrillogenesis regulator (MR-1) is overexpressed in human cancer cells and plays an essential role in cancer cell growth. However, its role in hepatocellular carcinoma (HCC) has not yet been explored. The aim of this study was to investigate the association of MR-1 expression with clinicopathologic features and prognosis in patients with HCC. Quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) was used to detect MR-1 mRNA levels in tissues samples from 120 HCC patients. Results showed that MR-1 expression was significantly higher in HCC tissues when compared with matched adjacent normal tissues (P=0.004). In HCC cancerous tissues, it was also significantly associated with tumor size (P=0.024) and serum AFP level (P=0.003). Moreover, Kaplan-Meier analysis showed that HCC patients with high MR-1 expression had shorter overall survival time than those with low MR-1 expression (P=0.009). When analyzed with a multivariate Cox regression model, MR-1 was identified as an independent prognostic factor for overall survival. Furthermore, when combined with serum AFP level, the median survival time significantly differed between patients with baseline high serum AFP and high MR-1 expression levels and those with normal AFP and low MR-1 levels (P=0.007). Taken together, our results suggest that high expression of MR-1 is involved in HCC progression and could be a novel biomarker of poor prognosis in patients with HCC.
肌原纤维生成调节因子(MR-1)在人类癌细胞中过表达,并且在癌细胞生长中发挥重要作用。然而,其在肝细胞癌(HCC)中的作用尚未得到探索。本研究的目的是调查MR-1表达与HCC患者临床病理特征及预后的相关性。采用定量逆转录聚合酶链反应(qRT-PCR)检测120例HCC患者组织样本中MR-1 mRNA水平。结果显示,与配对的癌旁正常组织相比,HCC组织中MR-1表达显著更高(P = 0.004)。在HCC癌组织中,它还与肿瘤大小(P = 0.024)和血清甲胎蛋白水平(P = 0.003)显著相关。此外,Kaplan-Meier分析显示,MR-1高表达的HCC患者总生存时间短于MR-1低表达的患者(P = 0.009)。当用多因素Cox回归模型分析时,MR-1被确定为总生存的独立预后因素。此外,当与血清甲胎蛋白水平相结合时,基线血清甲胎蛋白高且MR-1表达水平高的患者与甲胎蛋白正常且MR-1水平低的患者之间的中位生存时间有显著差异(P = 0.007)。综上所述,我们的结果表明,MR-1的高表达参与HCC进展,并且可能是HCC患者预后不良的一种新生物标志物。