Dai Meiyu, Li Limin, Qin Xue
Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530021, P.R. China.
Oncol Lett. 2019 Apr;17(4):3919-3929. doi: 10.3892/ol.2019.10024. Epub 2019 Feb 7.
The present study aimed to systematically analyze the value of microRNA-122 (miRNA-122) in the diagnosis and prognosis of hepatocellular carcinoma (HCC) and other types of cancer. First, the reverse transcription-quantitative polymerase chain reaction method was used to detect the expression levels of miRNA-122 in the serum samples of patients with HCC, benign lesions and healthy volunteers. Next, miRNA-seq data of miRNA-122 from The Cancer Genome Atlas database were used to analyze the differential expression and overall survival rate associated with a variety of types of cancer. Meanwhile, the target gene prediction of miRNA-122 was performed using four different software programs. Finally, 353 significant target genes were identified for Gene Ontology and Kyoto Encyclopedia of Genes and Genomes functional enrichment analysis. Finally, it was demonstrated that the expression levels of miRNA-122 in the HCC group were increased compared with the healthy group (P<0.001), but decreased with respect to the benign group (P<0.001). In addition, the combination of the miRNA-122 and a fetoprotein may further improve the diagnostic accuracy between the HCC and healthy groups (area under the curve, 0.980; 95% confidence interval, 0.958-1.000). It was also demonstrated that miRNA-122 exhibited significantly differential expression and the overall survival rate was predicted for various other types of cancer, including colorectal cancer, renal carcinoma, cholangiocarcinoma, prostate cancer and thyroid carcinoma. Functional enrichment analysis demonstrated that the target genes of miRNA-122 may contribute to the composition of the nucleus and cytoplasm, and regulate a variety of biological processes, including cardiac muscle cell differentiation and glucose metabolic processes via protein biosynthesis, estrogen and glucagon associated signaling pathways. These results revealed that miRNA-122 may be an indispensable biomarker for the diagnosis, prognostic evaluation and targeted therapy in pan-cancer.
本研究旨在系统分析微小RNA-122(miRNA-122)在肝细胞癌(HCC)及其他类型癌症诊断和预后中的价值。首先,采用逆转录-定量聚合酶链反应法检测HCC患者、良性病变患者及健康志愿者血清样本中miRNA-122的表达水平。其次,利用来自癌症基因组图谱数据库的miRNA-122的miRNA测序数据,分析与多种类型癌症相关的差异表达及总生存率。同时,使用四种不同软件程序对miRNA-122进行靶基因预测。最后,鉴定出353个显著靶基因用于基因本体论和京都基因与基因组百科全书功能富集分析。结果表明,HCC组中miRNA-122的表达水平高于健康组(P<0.001),但低于良性组(P<0.001)。此外,miRNA-122与甲胎蛋白联合使用可进一步提高HCC组与健康组之间的诊断准确性(曲线下面积,0.980;95%置信区间,0.958 - 1.000)。还表明miRNA-122在包括结直肠癌、肾癌、胆管癌、前列腺癌和甲状腺癌在内的多种其他类型癌症中表现出显著差异表达并可预测总生存率。功能富集分析表明,miRNA-122的靶基因可能参与细胞核和细胞质的组成,并通过蛋白质生物合成、雌激素和胰高血糖素相关信号通路调节多种生物学过程,包括心肌细胞分化和葡萄糖代谢过程。这些结果表明,miRNA-122可能是泛癌诊断、预后评估和靶向治疗中不可或缺的生物标志物。