Liang Yajun, Luo Jian, Hu Liya, Zhang Jun
IV Ward of Pulmonary and Critical Care Medicine Wuhan Pulmonary Hospital Wuhan China.
Department of Geriatrics Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.
J Cell Commun Signal. 2025 Apr 12;19(2):e70013. doi: 10.1002/ccs3.70013. eCollection 2025 Jun.
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.
肝细胞癌(HCC)是丙型肝炎病毒感染的严重后果,受到该病毒非结构蛋白3(NS3)的显著影响。本研究采用转录组测序,通过比较丙型肝炎病毒感染的肝癌组织与健康肝脏对照之间的基因表达谱,探索NS3在促进肝癌进展中的作用。通过定量逆转录PCR(RT-qPCR)和蛋白质免疫印迹分析鉴定并验证了受NS3调控的关键基因。进行了包括CCK-8、BrdU以及Transwell迁移和侵袭试验在内的功能分析,以评估NS3对肝癌细胞增殖、迁移和侵袭的影响。通过双荧光素酶报告基因和RNA下拉试验进一步研究发现,NS3特异性上调circ_0001175。这种环状RNA与miR-130a-5p相互作用并抑制它,通过调节MDM4途径减弱其对P53的调控作用,从而促进致癌特性。这些发现突出了NS3诱导的circ_0001175/miR-130a-5p/MDM4/P53途径作为潜在治疗靶点,为丙型肝炎病毒相关肝癌的治疗策略提供了有前景的方向。