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PKR-IN-C16 induces Epstein-Barr virus lytic infection via p38 MAPK-CREB pathway
Haige Han1, Yihan Zhang1, Hui Li1
1Frontiers Science Center for Molecular Design Breeding, College of Biological Sciences, China Agricultural University, Beijing, 100193, China; State Key Laboratory of Animal Biotech Breeding, College of Biological Sciences, China Agricultural University, Beijing, 100193, China; Ministry of Agriculture Key Laboratory of Soil Microbiology, College of Biological Sciences, China Agricultural University, Beijing, 100193, China; Department of Microbiology and Immunology, College of Biological Sciences, China Agricultural University, Beijing, 100193, China.
Abstract:
Epstein-Barr virus (EBV) is associated with tumors in its latency, and its switch from latency to lytic infection can induce host cell lysis. Therefore, the virus itself can become a potential target for EBV-associated tumors. In this study, we reported a small molecule compound, PKR-IN-C16 (C16), which was previously shown to be effective in treating neuronal inflammation and hepatocellular and colorectal carcinomas, had the ability to induce EBV lytic infection. We assessed its effects in both epithelial and lymphoid EBV-positive cells and found that it induced lytic infection and exerted killing effect on EBV-positive tumor cells in a dose-dependent manner by activating the EBV IE gene BZLF1- (Z-) and BRLF1- (R-) promoters. Subsequently, by pretreating the cells with signaling pathway inhibitors, we found that C16 induced lytic induction mainly through p38 MAPK pathway. The transcription factor CREB, downstream of the pathway, was phosphorylated and bound directly to activate the Z-promoter. Meanwhile, PKR knockdown was capable of inducing EBV lytic reactivation. Overall, our findings indicate that PKR-IN-C16 has the potential to serve as a lytic induction reagent for the treatment of EBV-associated tumors.
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