NS3 of hepatitis C virus drives hepatocellular carcinoma progression through a novel RNA-interference pathway

IF 3.9 3区 生物学 Q3 CELL BIOLOGY Journal of Cell Communication and Signaling Pub Date : 2025-04-12 DOI:10.1002/ccs3.70013
Yajun Liang, Jian Luo, Liya Hu, Jun Zhang
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Abstract

Hepatocellular carcinoma (HCC), a severe consequence of hepatitis C virus infection, is significantly influenced by the virus’s non-structural protein 3 (NS3). This study employed transcriptome sequencing to explore the role of NS3 in promoting HCC progression by comparing gene expression profiles between HCV-infected HCC tissues and healthy liver controls. Key genes regulated by NS3 were identified and validated with quantitative reverse transcription PCR (RT-qPCR) and western blot analyses. Functionality assays, including CCK-8, BrdU, and Transwell migration and invasion tests, were performed to evaluate the effects of NS3 on HCC cell proliferation, migration, and invasion. Further investigation through a dual-luciferase reporter and RNA pull-down assays revealed that NS3 specifically upregulates circ_0001175. This circular RNA interacts with and inhibits miR-130a-5p, diminishing its regulatory impact on P53 by modulating the MDM4 pathway, thereby promoting oncogenic characteristics. The findings highlight the NS3-induced circ_0001175/miR-130a-5p/MDM4/P53 pathway as a potential therapeutic target, offering promising directions for treatment strategies in HCV-related HCC.

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丙型肝炎病毒NS3通过一种新的rna干扰途径驱动肝细胞癌进展
肝细胞癌(HCC)是丙型肝炎病毒感染的一种严重后果,它受病毒非结构蛋白3 (NS3)的显著影响。本研究通过比较hcv感染的HCC组织和健康肝脏对照之间的基因表达谱,利用转录组测序技术探讨NS3在促进HCC进展中的作用。采用定量反转录PCR (RT-qPCR)和western blot方法对NS3调控的关键基因进行鉴定和验证。功能分析包括CCK-8、BrdU和Transwell迁移和侵袭试验,以评估NS3对HCC细胞增殖、迁移和侵袭的影响。通过双荧光素酶报告基因和RNA下拉实验进一步研究发现,NS3特异性上调circ_0001175。这种环状RNA与miR-130a-5p相互作用并抑制miR-130a-5p,通过调节MDM4通路减少其对P53的调控作用,从而促进致癌特性。这些发现强调了ns3诱导的circ_0001175/miR-130a-5p/MDM4/P53通路是一个潜在的治疗靶点,为hcv相关HCC的治疗策略提供了有希望的方向。
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来源期刊
CiteScore
6.40
自引率
4.90%
发文量
40
期刊介绍: The Journal of Cell Communication and Signaling provides a forum for fundamental and translational research. In particular, it publishes papers discussing intercellular and intracellular signaling pathways that are particularly important to understand how cells interact with each other and with the surrounding environment, and how cellular behavior contributes to pathological states. JCCS encourages the submission of research manuscripts, timely reviews and short commentaries discussing recent publications, key developments and controversies. Research manuscripts can be published under two different sections : In the Pathology and Translational Research Section (Section Editor Andrew Leask) , manuscripts report original research dealing with celllular aspects of normal and pathological signaling and communication, with a particular interest in translational research. In the Molecular Signaling Section (Section Editor Satoshi Kubota) manuscripts report original signaling research performed at molecular levels with a particular interest in the functions of intracellular and membrane components involved in cell signaling.
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