Wang Yajie, Gao Yingtang, Shi Wenxia, Zhai Daokuan, Rao Quan, Jia Xiaobo, Liu Jiao, Jiao Xiaolei, Du Zhi
Third Central Clinical College of Tianjin Medical University, Tianjin, China.
Key Laboratory of Artificial Cell, Institute for Hepatobiliary Disease, Third Central Hospital of Tianjin, Tianjin, China.
Cancer Biomark. 2015;15(2):171-80. doi: 10.3233/CBM-140451.
Abnormally expressed circulating microRNA (miRNA) may serve as a potential biomarker for the diagnosis of cancer patients.
We sought to determine the differentially expressed circulating microRNAs in patients with hepatitis B virus (HBV)-positive small hepatocellular carcinoma (HCC) compared to other HBV-positive benign liver diseases.
The miScript miRNA PCR Array was used to detect the levels of 84 miRNAs in plasma or serum samples of patients with HBV-related small HCC (23 cases), liver cirrhosis (LC) (20 cases), chronic hepatitis B (CHB) (20 cases) and healthy controls (16 cases). MiRNAs with fold-change values ⩾ 2 or ⩽ 0.5 compared to healthy controls were considered to be deregulated miRNAs.
The results of duplicate plasma experiments were not reliable. Comprehensive analysis of the two serum experiments showed that the quality controls all met the requirements. We found 18 differentially expressed miRNAs. Relative to healthy controls, nine, three, and 11 miRNAs were up-regulated in the CHB group, LC group and small HCC group, respectively. In contrast, one, three, and three miRNAs were down-regulated in the same patient groups, respectively. Interestingly, miR-195, miR-25 and miR-16 were up-regulated, and miR-205 was down-regulated, in all three experimental groups. Moreover, only in the HCC group, miR-18a, miR-100, miR-145 and miR-223 were up-regulated 3.48-, 2.95-, 2.12- and 3.91-fold, respectively, and miR-200a and miR-222 were down-regulated 2.56- and 2.00-fold, respectively.
Our study demonstrated the presence of six differentially expressed serum microRNAs in HBV-positive small HCC compared to other benign liver diseases associated with HBV.
循环微小RNA(miRNA)异常表达可能作为癌症患者诊断的潜在生物标志物。
我们试图确定与其他乙肝病毒(HBV)阳性良性肝病相比,HBV阳性小肝细胞癌(HCC)患者中差异表达的循环微小RNA。
采用miScript miRNA PCR芯片检测HBV相关小肝癌(23例)、肝硬化(LC,20例)、慢性乙型肝炎(CHB,20例)患者及健康对照(16例)血浆或血清样本中84种miRNA的水平。与健康对照相比,折叠变化值≥2或≤0.5的miRNA被认为是失调的miRNA。
重复血浆实验结果不可靠。对两次血清实验的综合分析表明,质量控制均符合要求。我们发现了18种差异表达的miRNA。与健康对照相比,CHB组、LC组和小肝癌组分别有9种、3种和11种miRNA上调。相反,同一患者组中分别有1种、3种和3种miRNA下调。有趣的是,在所有三个实验组中,miR-195、miR-25和miR-16均上调,而miR-205下调。此外,仅在肝癌组中,miR-18a、miR-100、miR-145和miR-223分别上调3.48倍、2.95倍、2.12倍和3.91倍,而miR-200a和miR-222分别下调2.56倍和2.00倍。
我们的研究表明,与其他HBV相关良性肝病相比,HBV阳性小肝癌患者血清中有6种差异表达的微小RNA。