Departments of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Departments of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Viruses. 2021 Apr 30;13(5):812. doi: 10.3390/v13050812.
Following our observation that clofoctol led to Epstein-Barr virus (EBV) lytic gene expression upon activation of the integrated stress response (ISR), we decided to investigate the impact of AsO on viral lytic gene expression. AsO has also been reported to activate the ISR pathway by its activation of the heme-regulated inhibitor (HRI). Our investigations show that AsO treatment leads to eIF2α phosphorylation, upregulation of ATF4 and TRB3 expression, and an increase of EBV Zta gene expression in lymphoid tumor cell lines as well as in naturally infected epithelial cancer cell lines. However, late lytic gene expression and virion production were blocked after arsenic treatment. In comparison, a small molecule HRI activator also led to increased Zta expression but did not block late lytic gene expression, suggesting that AsO effects on EBV gene expression are also mediated through other pathways.
在观察到氯氟醇可通过激活整合应激反应(ISR)导致 EBV 裂解基因表达后,我们决定研究砷对病毒裂解基因表达的影响。砷也已被报道通过激活血红素调节抑制剂(HRI)来激活 ISR 途径。我们的研究表明,砷处理导致 eIF2α 磷酸化、ATF4 和 TRB3 表达上调,以及 EBV Zta 基因在淋巴样肿瘤细胞系以及天然感染的上皮癌细胞系中的表达增加。然而,砷处理后晚期裂解基因表达和病毒粒子生成被阻断。相比之下,小分子 HRI 激活剂也导致 Zta 表达增加,但不阻断晚期裂解基因表达,这表明砷对 EBV 基因表达的影响也通过其他途径介导。