Liang Zenghui, Gao Yingtang, Shi Wenxia, Zhai Daokuan, Li Shilei, Jing Li, Guo Hua, Liu Tong, Wang Yajie, Du Zhi
Third Central Clinical College of Tianjin Medical University, Tianjin 300170, China.
ScientificWorldJournal. 2013 Oct 10;2013:381874. doi: 10.1155/2013/381874. eCollection 2013.
In our previous study, we found that some miRNAs were deregulated in hepatocellular carcinoma (HCC), including miR-183. However, the expression of miR-183 in the progression of benign liver diseases to HCC and its correlation with clinicopathologic factors remain undefined.
MiR-183 expression was measured in normal controls (NC) (n = 21), chronic viral hepatitis B or C (CH) tissues (n = 10), liver cirrhosis (LC) tissues (n = 18), HCC tissues (n = 92), and adjacent nontumor tissues (NT) (n = 92) by quantitative real-time reverse-transcription polymerase chain reaction (qRT-PCR).
The expression levels of miR-183 were significantly higher in HCC than in NT, LC, CH, and NL (P = 0.001, P < 0.001, P = 0.011, P < 0.001, resp.). The upregulated miR-183 in HCC was correlated with TNM stage (P = 0.042) and cirrhosis (P = 0.025). The Kaplan-Meier survival analysis showed that miR-183 expression was not associated with the survival of HCC patients. However, miR-183 yielded an area under the curve (AUC) of 0.808 with 59.8% sensitivity and 91.8% specificity in discriminating HCC from benign liver diseases (CH and LC) or NC.
The upregulated miR-183 may associate with onset and progression of HCC, but not with the patient survival. A further research is needed to determine the potential of miR-183 as biomarker for HCC.
在我们之前的研究中,我们发现一些微小RNA(miRNA)在肝细胞癌(HCC)中表达失调,包括miR-183。然而,miR-183在良性肝病进展为HCC过程中的表达及其与临床病理因素的相关性仍不明确。
通过定量实时逆转录聚合酶链反应(qRT-PCR)检测正常对照(NC)(n = 21)、慢性乙型或丙型病毒性肝炎(CH)组织(n = 10)、肝硬化(LC)组织(n = 18)、HCC组织(n = 92)及癌旁非肿瘤组织(NT)(n = 92)中miR-183的表达。
HCC中miR-183的表达水平显著高于NT、LC、CH及NC(分别为P = 0.001、P < 0.001、P = 0.011、P < 0.001)。HCC中miR-183上调与TNM分期(P = 0.042)及肝硬化(P = 0.025)相关。Kaplan-Meier生存分析显示,miR-183表达与HCC患者的生存无关。然而,在区分HCC与良性肝病(CH和LC)或NC时,miR-183的曲线下面积(AUC)为0.808,敏感性为59.8%,特异性为91.8%。
miR-183上调可能与HCC的发生和进展相关,但与患者生存无关。需要进一步研究以确定miR-183作为HCC生物标志物的潜力。