Li Tao, Yin Jikai, Yuan Lijuan, Wang Shouli, Yang Lin, Du Xilin, Lu Jianguo
Department of General Surgery, Tangdu Hospital of The Fourth Military Medical University, Xi'an, Shaanxi 710038, P.R. China.
Oncol Rep. 2014 Apr;31(4):1699-706. doi: 10.3892/or.2014.3032. Epub 2014 Feb 19.
MicroRNAs (miRNAs) have been frequently reported to be diagnostic biomarkers and prognostic factors for cancer. The aim of the present study was to evaluate the clinical significance of microRNA-139 (miRNA-139) in hepatocellular carcinoma (HCC). All 31 patients enrolled in the present study had received curative hepatectomy. The objective miRNA was determined using miRNA microarray. The miRNA-139 expression level in cancerous tissue specimens was measured by means of reverse transcription and quantitative polymerase chain reaction, and compared with that in 31 corresponding peritumoral non-cancerous tissues. Plasma miRNA-139 expression was also quantified. The diagnostic value of plasma miRNA-139 for differentiating patients with HCC from the ones with chronic HBV-hepatitis (CH) was analyzed. The miRNA microarray performed in 3 pairs of tissue specimens determined miRNA-139 was downregulated (p=0.017). Compared with plasma of chronic HBV-hepatitis, miRNA-139 was lowly expressed in plasma of HCC patients (p<0.010). ROC analysis of plasma miRNA-139 yielded an AUC of 0.764 (p<0.010) with sensitivity of 80.6% and specificity of 58.1% while differentiating HCC from chronic HBV-hepatitis. The diagnostic power of serum α-fetoprotein (AFP) was also evaluated. The combination of miRNA-139 and AFP improved the differentiating power. Subsequently, 31 HCC patients were divided into the low or high expression group based on plasma miRNA-139 level. Plasma miRNA‑139 expression was correlated with serum AFP (p=0.043), Edmondson-Steiner grading (p=0.038). In addition, there was a significant difference in the 1-year survival rates between the two groups (p=0.023). miRNA‑139 was downregulated in the cancerous tissue and plasma of HCC patients. Plasma miRNA‑139 is a diagnostic biomarker and prognostic factor for HCC.
微小RNA(miRNA)经常被报道为癌症的诊断生物标志物和预后因素。本研究的目的是评估微小RNA - 139(miRNA - 139)在肝细胞癌(HCC)中的临床意义。本研究纳入的31例患者均接受了根治性肝切除术。使用miRNA微阵列确定目标miRNA。通过逆转录和定量聚合酶链反应测量癌组织标本中miRNA - 139的表达水平,并与31例相应的癌旁非癌组织中的表达水平进行比较。还对血浆miRNA - 139表达进行了定量。分析了血浆miRNA - 139对区分HCC患者与慢性乙型肝炎(CH)患者的诊断价值。在3对组织标本中进行的miRNA微阵列检测确定miRNA - 139表达下调(p = 0.017)。与慢性乙型肝炎患者的血浆相比,HCC患者血浆中miRNA - 139表达较低(p < 0.010)。血浆miRNA - 139的ROC分析得出AUC为0.764(p < 0.010),在区分HCC与慢性乙型肝炎时敏感性为80.6%,特异性为58.1%。还评估了血清甲胎蛋白(AFP)的诊断效能。miRNA - 139和AFP联合使用提高了鉴别能力。随后,根据血浆miRNA - 139水平将3例HCC患者分为低表达组或高表达组。血浆miRNA - 139表达与血清AFP(p = 0.043)、Edmondson - Steiner分级(p = 0.038)相关。此外,两组之间的1年生存率存在显著差异(p = 0.023)。miRNA - 139在HCC患者的癌组织和血浆中表达下调。血浆miRNA - 139是HCC的诊断生物标志物和预后因素。