Li Yueshuo, Shi Feng, Hu Jianmin, Xie Longlong, Bode Ann M, Cao Ya
Key Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Department of Otolaryngology Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha 410078, China.
Cancer Research Institute and School of Basic Medical Science, Xiangya School of Medicine, Central South University, Changsha 410078, China.
J Oncol. 2019 Jul 18;2019:2128410. doi: 10.1155/2019/2128410. eCollection 2019.
Infection-related cancer comprises one-sixth of the global cancer burden. Oncoviruses can directly or indirectly contribute to tumorigenesis. Ubiquitination is a dynamic and reversible posttranslational modification that participates in almost all cellular processes. Hijacking of the ubiquitin system by viruses continues to emerge as a central theme around the viral life cycle. Deubiquitinating enzymes (DUBs) maintain ubiquitin homeostasis by removing ubiquitin modifications from target proteins, thereby altering protein function, stability, and signaling pathways, as well as acting as key mediators between the virus and its host. In this review, we focus on the multiple functions of DUBs in RIG-I-like receptors (RLRs) and stimulator of interferon genes (STING)-mediated antiviral signaling pathways, oncoviruses regulation of NF-B activation, oncoviral life cycle, and the potential of DUB inhibitors as therapeutic strategies.
感染相关癌症占全球癌症负担的六分之一。致癌病毒可直接或间接促进肿瘤发生。泛素化是一种动态且可逆的翻译后修饰,几乎参与所有细胞过程。病毒对泛素系统的劫持已逐渐成为围绕病毒生命周期的核心主题。去泛素化酶(DUBs)通过去除靶蛋白上的泛素修饰来维持泛素稳态,从而改变蛋白质功能、稳定性和信号通路,同时还作为病毒及其宿主之间的关键介质。在本综述中,我们重点关注DUBs在维甲酸诱导基因I样受体(RLRs)和干扰素基因刺激因子(STING)介导的抗病毒信号通路中的多种功能、致癌病毒对核因子κB(NF-κB)激活的调控、致癌病毒生命周期以及DUB抑制剂作为治疗策略的潜力。