The Role of ZNF207 in Liver Hepatocellular Carcinoma: Expression Analysis and Prognostic Implications

Chengrui Peng, Linfei Wu, Xiaofang Yang, Hanyun Yao, Yan Xie
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Abstract

Objective: To analyze the expression and clinical significance of the zinc finger protein ZNF207 gene in liver hepatocellular carcinoma (LIHC) based on The Cancer Genome Atlas (TCGA) database. Methods: The mRNA sequencing data of 371 cases of primary liver cancer, 50 cases of normal tissues, and 3 cases of recurrent liver cancer were downloaded from the TCGA database. The corresponding clinical information of the 371 cases of hepatocellular carcinoma was subsequently analyzed. The difference in ZNF207 expression between normal and tumor tissues was analyzed using the UALCAN online database. The impact of ZNF207 expression on survival prognosis was assessed using the Kaplan-Meier method in R software. The GO and KEGG pathways of ZNF207 were analyzed. The Cox proportional hazards model was used to evaluate the prognostic factors of patients with LIHC. RT-qPCR was employed to verify the expression of ZNF207 in LIHC cells. Results: ZNF207 was highly expressed in LIHC tissues and HepG2 cells, with a significant difference (P <  0.05). Multivariate Cox regression analysis revealed that patients with high ZNF207 expression had a significantly shorter overall survival time compared to those with low ZNF207 expression (HR = 1.466, 95% CI: 1.011–2.126, P < 0.05). GO enrichment analysis suggested that ZNF207 may influence the onset and progression of hepatocellular carcinoma by regulating mRNA splicing and mRNA transcription processing through the spliceosome. KEGG pathway enrichment analysis indicated that ZNF207 might affect the onset and progression of hepatocellular carcinoma through mitophagy, mRNA surveillance, homologous recombination, spliceosome, and nuclear-cytoplasmic transport. Conclusion: The expression of ZNF207 may be an independent predictor of the prognosis of patients with LIHC and could influence the development of hepatocellular carcinoma through various gene functions and pathways. It has the potential to serve as a novel molecular marker for predicting the prognosis of hepatocellular carcinoma.
ZNF207 在肝脏肝细胞癌中的作用:表达分析和预后意义
目的基于癌症基因组图谱(TCGA)数据库,分析锌指蛋白ZNF207基因在肝肝细胞癌(LIHC)中的表达及临床意义。研究方法从TCGA数据库下载371例原发性肝癌、50例正常组织和3例复发性肝癌的mRNA测序数据。随后分析了 371 例肝癌的相应临床信息。利用 UALCAN 在线数据库分析了正常组织和肿瘤组织中 ZNF207 表达的差异。用R软件中的Kaplan-Meier法评估了ZNF207表达对生存预后的影响。分析了ZNF207的GO和KEGG通路。采用Cox比例危险模型评估LIHC患者的预后因素。采用 RT-qPCR 验证 ZNF207 在 LIHC 细胞中的表达。结果显示ZNF207在LIHC组织和HepG2细胞中高表达,差异显著(P < 0.05)。多变量 Cox 回归分析显示,ZNF207 高表达患者的总生存时间明显短于 ZNF207 低表达患者(HR = 1.466,95% CI:1.011-2.126,P <0.05)。GO富集分析表明,ZNF207可能通过剪接体调控mRNA剪接和mRNA转录处理,从而影响肝细胞癌的发生和发展。KEGG通路富集分析表明,ZNF207可能通过有丝分裂、mRNA监控、同源重组、剪接体和核-胞质转运影响肝细胞癌的发生和发展。结论ZNF207的表达可能是预测LIHC患者预后的独立指标,并可通过各种基因功能和途径影响肝细胞癌的发展。它有望成为预测肝细胞癌预后的新型分子标记物。
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