Yu Liang, Zhang Mei, Ma Zhenhua, Wu Shengli
Department of Hepatobiliary Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China.
Oncol Lett. 2023 Dec 12;27(2):55. doi: 10.3892/ol.2023.14188. eCollection 2024 Feb.
Small nucleolar RNA H/ACA Box 51 (SNORA51) is involved in progression of multiple cancers. However, its role in hepatocellular carcinoma (HCC) is still unclear. The aim of the present study was to analyze the expression of SNORA51 in HCC and its clinical significance. A total of 136 patients with HCC who underwent surgery from January 1, 2016 to December 31, 2018 were included. The expression of SNORA51 in cancer tissues and adjacent tissues was compared using reverse transcription-quantitative PCR and bioinformatics methods. Methylation of the SNORA51 promoter in cancer and adjacent tissues was compared using bioinformatics. The relationship between SNORA51 expression levels and clinicopathological characteristics of patients with HCC, in addition to prognosis, was analyzed. The expression of SNORA51 in HCC was significantly higher compared with that in adjacent tissues (P<0.05). starBase demonstrated that higher expression levels of SNORA51 were associated with a significantly worse prognosis of patients with HCC compared with those who had lower expression levels of SNORA51 (P<0.05). Bioinformatics analysis using The University of Alabama at Birmingham Cancer Data Analysis Portal demonstrated that methylation of the SNORA51 promoter region in HCC was significantly decreased compared with adjacent tissues (P<0.05). A high expression of SNORA51 was significantly associated with portal vein tumor thrombus, vascular invasion and TNM stage (P<0.05). The median survival time of patients with high SNORA51 expression was significantly lower compared with those who had low SNORA51 expression (P<0.05). Both uni- and multivariate Cox regression analysis demonstrated that SNORA51 expression was an independent risk factor that significantly worsened the prognosis of patients with HCC (P<0.05). The overexpression of SNORA51 in patients with HCC was significantly associated with a poor prognosis and may be related to the reduced methylation of the SNORA51 promoter region. Therefore, SNORA51 may be a promising biomarker for prediction of the prognosis of patients with HCC and may be a therapeutic target for the treatment of HCC in future.
小核仁RNA H/ACA盒51(SNORA51)参与多种癌症的进展。然而,其在肝细胞癌(HCC)中的作用仍不清楚。本研究的目的是分析SNORA51在HCC中的表达及其临床意义。纳入了2016年1月1日至2018年12月31日期间接受手术的136例HCC患者。采用逆转录定量PCR和生物信息学方法比较癌组织和癌旁组织中SNORA51的表达。使用生物信息学比较癌组织和癌旁组织中SNORA51启动子的甲基化情况。分析了SNORA51表达水平与HCC患者临床病理特征以及预后之间的关系。与癌旁组织相比,HCC中SNORA51的表达明显更高(P<0.05)。starBase显示,与SNORA51表达水平较低的患者相比,SNORA51表达水平较高的HCC患者预后明显更差(P<0.05)。使用阿拉巴马大学伯明翰分校癌症数据分析门户进行的生物信息学分析表明,与癌旁组织相比,HCC中SNORA51启动子区域的甲基化明显降低(P<0.05)。SNORA51高表达与门静脉癌栓、血管侵犯和TNM分期显著相关(P<0.05)。SNORA51高表达患者的中位生存时间明显低于SNORA51低表达患者(P<0.05)。单因素和多因素Cox回归分析均表明,SNORA51表达是一个独立的危险因素,显著恶化HCC患者的预后(P<0.05)。HCC患者中SNORA51的过表达与不良预后显著相关,可能与SNORA51启动子区域甲基化降低有关。因此,SNORA51可能是预测HCC患者预后的有前景的生物标志物,未来可能成为HCC治疗的靶点。