丙型肝炎病毒NS3蛋白对肝细胞癌标志物热休克蛋白70和Glypican3表达的影响

Sepideh Saeb, F. Sabahi, Z. Mazaheri, M. Ravanshad
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引用次数: 0

摘要

背景与目的:丙型肝炎病毒(HCV)感染是肝癌发生的重要危险因素。HCV NS3蛋白在病毒生命周期中起着关键作用,可以影响正常的细胞活动,如细胞增殖、细胞死亡和细胞信号通路。此外,它可能影响恶性肿瘤的发展。本研究评估的两个细胞基因热休克蛋白70 (HSP70)和Glypican3 (GPC3)在细胞信号通路调控中发挥重要作用,包括细胞增殖。本研究旨在评估HCV NS3蛋白在Balb/C小鼠模型中对这两个基因表达的影响。材料与方法:本研究采用Balb/C雄性小鼠3组(n=8)。第一组注射NS3质粒,第二组注射乙型肝炎病毒HBx质粒,阴性对照组注射蒸馏水。通过尾静脉注射两次,最后一次注射后,从肝组织中提取RNA。接下来,对相关基因进行cDNA合成和实时聚合酶链反应。结果:与阴性对照组相比,NS3组所选基因相对表达量显著(GPC3 P=0.0229, HSP70 P= 0.0020)。而NS3组与HBx组间无显著差异(GPC3组P=0.4516, HSP70组P= 0.6740)。结论:结果表明NS3蛋白可能影响上述基因的表达增加。然而,为了更准确地了解NS3,还需要进行更多的研究,如评估NS3对细胞信号通路中其他相关蛋白的影响,研究NS3的其他结构域,进行病理和组织学检查,使用各种实验方法,评估NS4A作为NS3的辅助因子的作用,以及使用更稳定的载体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of hepatitis C virus NS3 protein on expression of heat shock protein 70 and Glypican3 as the markers of hepatocellular carcinoma
Background and Aims: Hepatitis C virus (HCV) infection is an important risk factor for the development of liver cancer. The HCV NS3 protein plays a key role in the virus life cycle and can affect normal cellular activities, such as cell proliferation, cell death, and cell signaling pathways. Moreover, it may influence malignancy development. Two cellular genes, heat shock protein 70 (HSP70) and Glypican3 (GPC3), that are assessed in this study, play important roles in the regulation of the cell signaling pathways, including cell proliferation. This study aimed to evaluate the effects of HCV NS3 protein on the expressions of these two genes in the Balb/C mouse model. Materials and Methods: This study was performed on three groups of male mice of Balb/C (n=8). The first group received NS3 plasmid, the second group received hepatitis B virus HBx plasmid, and the negative control group received distilled water. Two injections were administered via the tail vein, and after the last injection, RNA was extracted from the liver tissue. Next, the cDNA synthesis and real-time polymerase chain reaction for relevant genes were performed. Results: Findings revealed that the relative expression of the selected genes in the NS3 group was significant in comparison with the negative control group (P=0.0229 for GPC3 and 0.0020 for HSP70). However, there was no significant difference between the NS3 group and the HBx group (P=0.4516 for GPC3 and 0.6740 for HSP70). Conclusion: Results showed that NS3 protein may affect the increasing expression of the mentioned genes. Nevertheless, for more precise understanding, much more studies should be performed, such as evaluation of the effect of NS3 on other involved proteins in cell signaling pathways, studying other domains of NS3, performance of pathological and histological tests, usage of various experimental methods, assessment of the role of NS4A as a cofactor for NS3, and usage of vectors with more stability.
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