Identification and Verification of Ubiquitin D as a Gene Associated with Hepatitis C Virus-Induced Hepatocellular Carcinoma.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2022-01-01 Epub Date: 2022-06-21 DOI:10.1159/000525543
Huanqin Li, Shumin Liu, Yun Lin, Xiongfei Shi, Na Du, Jing Yao, Ruiyang Liu, Yan Du, Kai Yang
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引用次数: 1

Abstract

Introduction: Accumulated studies have suggested that hepatitis C virus (HCV) infection is one of the leading causes for hepatocellular carcinoma (HCC). However, the mechanisms underlying the effect of HCV on the occurrence of HCC are still poorly understood.

Methods: HCV infection datasets (GSE82177 and GSE17856) and HCC datasets (The Cancer Genome Atlas Liver Hepatocellular Carcinoma and GSE89377) were downloaded from Gene Expression Omnibus or TCGA for analysis. The common differentially expressed genes in the above four datasets were identified by R software. The expression of ubiquitin D (UBD) in HCV-infected HepG2 cells was detected by RT-qPCR and Western blot, respectively. The interaction between NS3 and p53 was detected by co-immunoprecipitation. The influence of UBD on the proliferation and migration ability of HepG2 cells was evaluated by CCK-8 and wound healing assay, respectively.

Results: UBD was upregulated in both HCV-infected samples and HCC samples. HCV NS3 interacted with p53 and inhibited its expression. HCV NS3-induced UBD promoted the proliferation and migration of HepG2 cells.

Conclusion: Our results suggest that HCV NS3-induced UBD is positively correlated with the development of HCV-related HCC during HCV infection. Targeting UBD could be a potential strategy for preventing and treating HCV-induced HCC.

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泛素D与丙型肝炎病毒诱导的肝细胞癌相关基因的鉴定和验证
大量研究表明丙型肝炎病毒(HCV)感染是导致肝细胞癌(HCC)的主要原因之一。然而,HCV对HCC发生影响的潜在机制仍然知之甚少。方法:从Gene Expression Omnibus或TCGA下载HCV感染数据集(GSE82177和GSE17856)和HCC数据集(The Cancer Genome Atlas Liver hepatellular Carcinoma和GSE89377)进行分析。以上4个数据集中的共同差异表达基因通过R软件进行鉴定。采用RT-qPCR和Western blot分别检测hcv感染HepG2细胞中泛素D (ubiquitin D, UBD)的表达。采用共免疫沉淀法检测NS3与p53的相互作用。CCK-8和创面愈合实验分别评价UBD对HepG2细胞增殖和迁移能力的影响。结果:UBD在hcv感染样本和HCC样本中均上调。HCV NS3与p53相互作用,抑制其表达。HCV ns3诱导的UBD可促进HepG2细胞的增殖和迁移。结论:我们的研究结果提示HCV ns3诱导的UBD与HCV感染期间HCV相关HCC的发生呈正相关。靶向UBD可能是预防和治疗hcv诱导的HCC的潜在策略。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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