El-Abd Nevine E, Fawzy Nahla A, El-Sheikh Suzan M, Soliman Mohamed E
Kasr Al-Ainy School of Medicine, Cairo University, Cairo, Egypt,
Mol Diagn Ther. 2015 Aug;19(4):213-20. doi: 10.1007/s40291-015-0148-1.
Hepatocellular carcinoma (HCC) is the sixth most common cancer in the world. Having a very poor prognosis, it currently ranks as the third most common cause of cancer-related deaths. MiRNAs are a set of small, single-stranded, non-coding RNA molecules that negatively regulate gene expression at the post-transcriptional level. Several miRNAs were found to be frequently deregulated in HCC.
To investigate whether miRNA-122, miRNA-199a, and miRNA-16 are altered in sera of hepatitis C virus (HCV)-induced HCC patients compared with chronic HCV patients without HCC, and to assess their diagnostic value to differentiate between HCC and chronic HCV in order to develop a non-invasive diagnostic and prognostic tool for HCC.
We analysed the expression of mature miRNA-122, miRNA-199a, and miRNA-16 in serum by a singleplex TaqMan two-step stem loop quantitative real-time reverse-transcription PCR (qRT-PCR) in 40 newly diagnosed HCC patients and 40 chronic HCV liver cirrhosis patients, as well as 20 apparently healthy individuals as a control group, using RNU48 as a normalisation control.
Serum miR-16 was significantly lower in HCC than in HCV patients (P = 0.033). The serum level of miR-199a in chronic HCV patients was significantly lower than in healthy controls (P = 0.001). Receiver operating curve (ROC) analysis for serum miRNA-16 for discriminating HCC from HCV patients showed that at the cut-off value of 0.904, the sensitivity and specificity for this marker were 57.5 and 70 %, respectively. The combination of serum miR-16 with serum alpha fetoprotein (AFP) resulted in improved sensitivity to 85% and increased diagnostic accuracy to 87.5 %. Serum miR-199a and miR-16 were significantly associated with several parameters of HCC such as tumour size and number.
The combination of serum miR-16 and serum AFP is a significant improvement on the current best practice of serum AFP for HCC in HCVpositive patients. Serum miR-199a and miR-16 could be used as potential indicators of the progress of HCC.
肝细胞癌(HCC)是全球第六大常见癌症。其预后很差,目前是癌症相关死亡的第三大常见原因。微小RNA(miRNA)是一组小的单链非编码RNA分子,在转录后水平负向调节基因表达。已发现几种miRNA在HCC中经常失调。
研究与无HCC的慢性丙型肝炎病毒(HCV)患者相比,HCV诱导的HCC患者血清中miRNA-122、miRNA-199a和miRNA-16是否发生改变,并评估它们在区分HCC和慢性HCV方面的诊断价值,以便开发一种用于HCC的非侵入性诊断和预后工具。
我们采用单重TaqMan两步茎环定量实时逆转录PCR(qRT-PCR)分析了40例新诊断的HCC患者、40例慢性HCV肝硬化患者以及20名明显健康个体(作为对照组)血清中成熟miRNA-122、miRNA-199a和miRNA-16的表达,以RNU48作为标准化对照。
HCC患者血清miR-16显著低于HCV患者(P = 0.033)。慢性HCV患者血清miR-199a水平显著低于健康对照(P = 0.001)。血清miRNA-16区分HCC与HCV患者的受试者工作特征曲线(ROC)分析表明,在临界值为0.904时,该标志物的敏感性和特异性分别为57.5%和70%。血清miR-16与血清甲胎蛋白(AFP)联合使用可使敏感性提高到85%,诊断准确性提高到87.5%。血清miR-199a和miR-16与HCC的几个参数如肿瘤大小和数量显著相关。
血清miR-16与血清AFP联合使用对HCV阳性患者HCC的当前最佳血清AFP检测方法有显著改进。血清miR-199a和miR-16可作为HCC进展的潜在指标。