Kamel Marwa M, Matboli Marwa, Sallam Maha, Montasser Iman F, Saad Amr S, El-Tawdi Ahmed H F
Oncology Diagnostic Unit, Medical Biochemistry and Molecular Biology Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Oncology Diagnostic Unit, Medical Biochemistry and Molecular Biology Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Transl Res. 2016 Feb;168:134-145. doi: 10.1016/j.trsl.2015.10.002. Epub 2015 Oct 24.
There is an increasing interest in using long noncoding RNAs (lncRNAs) as biomarkers in cancer. Predictive biomarkers in hepatocellular carcinoma (HCC) have great benefit in the choice of therapeutic modality for HCC. The aim of this study is to assess lncRNA-urothelial carcinoma associated-1 (lncRNA-UCA1) and WD repeat containing, antisense to TP53 (WRAP53) expression as novel noninvasive biomarkers for diagnosis of HCC in sera of HCC patients compared with chronic hepatitis C virus (HCV) patients and healthy volunteers and to analyze their relationship with respect to the clinicopathologic features. We retrieved HCC characteristic lncRNAs, lncRNA-UCA1 and lncRNA-WRAP53, based on the microarray signature profiling (released by LncRNADisease database). Quantitative reverse-transcriptase polymerase chain reaction assay (RT-qPCR) was then used to evaluate the expression of selected lncRNAs in the serum of 160 participants. Furthermore, in 20 of 82 HCC cases involved in the study, we examined the expression of lncRNA-UCA1 and lncRNA-WRAP53 in 20 HCC tissues and adjacent nontumor tissues and analyzed its correlation with the serum level of these lncRNAs. The prognostic significance of the investigated parameters in HCC patients was explored. We found that lncRNA-UCA1 and lncRNA-WRAP53 were significantly higher in sera of HCC than those with chronic HCV infection or healthy volunteers. Our data suggested that the increased expression of UCA1 and WRAP53 was associated with advanced clinical parameters in HCC. Of note, tissue levels of the chosen lncRNAs strongly correlate with their sera level. The combination of both lncRNAs with serum alpha fetoprotein resulted in improved sensitivity to 100%. The median follow-up period was 21.5 months. LncRNA-WRAP53 was significant independent prognostic markers in relapse-free survival. LncRNA-UCA1 and lncRNA-WRAP53 upregulation may serve as novel serum biomarkers for HCC diagnosis and prognosis.
将长链非编码RNA(lncRNA)用作癌症生物标志物的兴趣与日俱增。肝细胞癌(HCC)中的预测性生物标志物对HCC治疗方式的选择大有裨益。本研究旨在评估尿路上皮癌相关lncRNA-1(lncRNA-UCA1)和含WD重复序列且为TP53反义链的lncRNA(WRAP53)的表达,将其作为与慢性丙型肝炎病毒(HCV)患者及健康志愿者相比,用于诊断HCC患者血清中HCC的新型非侵入性生物标志物,并分析它们与临床病理特征的关系。我们基于微阵列特征谱分析(由LncRNADisease数据库发布)检索了HCC特征性lncRNA,即lncRNA-UCA1和lncRNA-WRAP53。然后使用定量逆转录聚合酶链反应分析(RT-qPCR)评估160名参与者血清中所选lncRNA的表达。此外,在本研究涉及的82例HCC病例中的20例中,我们检测了20例HCC组织及相邻非肿瘤组织中lncRNA-UCA1和lncRNA-WRAP53的表达,并分析了其与这些lncRNA血清水平的相关性。探讨了所研究参数在HCC患者中的预后意义。我们发现HCC患者血清中的lncRNA-UCA1和lncRNA-WRAP53显著高于慢性HCV感染患者或健康志愿者。我们的数据表明,UCA1和WRAP53表达增加与HCC的晚期临床参数相关。值得注意的是,所选lncRNA的组织水平与其血清水平密切相关。两种lncRNA与血清甲胎蛋白联合使用可使敏感性提高至100%。中位随访期为21.5个月。lncRNA-WRAP53是无复发生存的显著独立预后标志物。lncRNA-UCA1和lncRNA-WRAP53上调可能作为HCC诊断和预后的新型血清生物标志物。