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ChemicalBook >> journal list >> NPJ Precision Oncology >>article
NPJ Precision Oncology

NPJ Precision Oncology

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Upregulated PrPC by HBx enhances NF-κB signal via liquid–liquid phase separation to advance liver cancer

Published:27 September 2024 DOI: 10.1038/s41698-024-00697-5
Yang Liu, Jing Zhang, Zixu Zhai, Chenyi Liu, Siqi Yang, Ying Zhou, Xianhuang Zeng, Jiaqi Liu, Xiaoyu Zhang, Xinqi Nie, Jiaqi Xu, Junsong Huang, Chaozhi Liu, Zhepeng Liu, Mingxiong Guo, Guihong Sun

Abstract

Cellular prion protein (PrPC) has been implicated in carcinogenic through the activation of various signal pathways, however, the precise mechanisms remain elusive. In vitro studies have shown that PrPC is prone to undergo liquid-liquid phase separation (LLPS). However, it remains unknown whether PrPC contributes to LLPS-inducing cancer development. Herein, we observed an upregulation of PrPC expression in hepatitis B virus-positive hepatocellular carcinoma (HCC). Subsequent investigation revealed that HBx of HBV enhances PrPC expression in a dose-dependent manner by binding to CREB1. Furthermore, we demonstrated that PrPC undergoes LLPS and recruits TRAF2/6, TAB2/3, and TAK1 protein, thereby activating the NF-κB signaling pathway and promoting tumor progression. Notably, although unable to undergo LLPS itself, the α3 helix of PrPC is essential for its activation of the NF-κB signaling pathway during the LLPS process. Further analysis unveiled that disulfide bond formation within the C-terminal domain of PrPC is necessary for its LLPS and subsequent activation of the NF-κB signaling pathway. Additionally, our findings indicate that NF-κB activation by PrPC condensates leads to increased IL-8 expression which further promotes tumor development.

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