H/ACA snoRNP Gene Family as Diagnostic and Prognostic Biomarkers for Hepatocellular Carcinoma.

Pharmacogenomics and Personalized Medicine Pub Date : 2021-10-19 eCollection Date: 2021-01-01 DOI:10.2147/PGPM.S333838
Mi Zhang, Wei Zhao, Shanshan Liu, Haichuan Liu, Liang Liu, Qiling Peng, Chengyou Du, Ning Jiang
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引用次数: 7

Abstract

Background The H/ACA small nucleolar ribonucleoprotein (snoRNP) gene family, including GAR1 ribonucleoprotein (GAR1), NHP2 ribonucleoprotein (NHP2), NOP10 ribonucleoprotein (NOP10), and dyskerin pseudouridine synthase 1 (DKC1), play important roles in ribosome biogenesis. However, the potential clinical value of the H/ACA snoRNP gene family in hepatocellular carcinoma (HCC) has not yet been reported. Methods Bioinformation databases were used to analyze the expression and roles of the H/ACA snoRNP gene family in HCC. Survival analysis, Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes enrichment pathway (KEGG) analyses were performed using R software. Tumor Immune Estimation Resource (TIMER) was used to analyze the correlation between the expression of the H/ACA snoRNP gene family and immune infiltration in HCC. Finally, immunohistochemistry and Western blotting were performed to verify the protein expression of the H/ACA snoRNP gene family in HCC tissues and adjacent tissues. Results The expression of the H/ACA snoRNP gene family was significantly increased in HCC samples compared to normal tissues, and the area under the curve (AUC) of GAR1, NHP2, NOP10, and DKC1 was 0.898, 0.962, 0.884, and 0.911, respectively. Increased expression of the H/ACA snoRNP gene family was associated with poor prognosis in HCC patients (Hazard Ratio, HR = 1.44 [1.02–2.04], 1.70 [1.20–2.40], 1.53 [1.09–2.17], and 1.43 [1.02–2.03], respectively; log-rank P = 0.036, 0.003, 0.014, 0.039, respectively). GO and KEGG analyses showed that co-expressed genes were primarily enriched in ribosome biogenesis. In addition, upregulated expression of H/ACA snoRNP gene family was related to the infiltration of various immune cells and multiple T cell exhaustion markers in HCC patients. Immunohistochemical analysis and Western blotting showed that the protein expression of H/ACA snoRNP gene family was higher in HCC tissues than in adjacent tissues of clinical samples. Conclusion H/ACA snoRNP gene family expression was higher in HCC tissues than in normal or adjacent tissues and was highly associated with poor prognosis of HCC patients and, therefore, has the potential to serve as diagnostic and prognostic biomarkers for HCC.

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H/ACA snoRNP基因家族作为肝细胞癌诊断和预后的生物标志物
背景:H/ACA小核仁核糖核蛋白(snoRNP)基因家族,包括GAR1核糖核蛋白(GAR1)、NHP2核糖核蛋白(NHP2)、NOP10核糖核蛋白(NOP10)和dyskerin伪尿嘧啶合成酶1 (DKC1),在核糖体生物发生中起重要作用。然而,H/ACA snoRNP基因家族在肝细胞癌(HCC)中的潜在临床价值尚未见报道。方法:应用生物信息库分析H/ACA snoRNP基因家族在HCC中的表达及作用。使用R软件进行生存分析、基因本体(GO)和京都基因与基因组富集途径百科全书(KEGG)分析。采用肿瘤免疫估计资源(Tumor Immune Estimation Resource, TIMER)分析H/ACA snoRNP基因家族表达与肝癌免疫浸润的相关性。最后通过免疫组化和Western blotting验证H/ACA snoRNP基因家族在HCC组织及癌旁组织中的蛋白表达。结果:H/ACA snoRNP基因家族在HCC样本中的表达较正常组织明显升高,GAR1、NHP2、NOP10、DKC1的曲线下面积(AUC)分别为0.898、0.962、0.884、0.911。H/ACA snoRNP基因家族表达增高与HCC患者预后不良相关(风险比,HR分别为1.44[1.02-2.04]、1.70[1.20-2.40]、1.53[1.09-2.17]、1.43 [1.02-2.03];log-rank P分别= 0.036,0.003,0.014,0.039)。GO和KEGG分析显示,共表达基因主要富集于核糖体生物发生中。此外,H/ACA snoRNP基因家族表达上调与HCC患者多种免疫细胞浸润及多种T细胞衰竭标志物有关。免疫组化分析和Western blotting显示,H/ACA snoRNP基因家族蛋白在HCC组织中的表达高于临床标本的邻近组织。结论:H/ACA snoRNP基因家族在HCC组织中的表达高于正常或癌旁组织,且与HCC患者预后不良高度相关,具有作为HCC诊断和预后生物标志物的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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