Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC, United States; Department of Pharmacology, The University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Adv Virus Res. 2021;109:201-254. doi: 10.1016/bs.aivir.2020.10.001. Epub 2020 Nov 9.
The DNA viruses, Kaposi's sarcoma-associated herpesvirus (KSHV) and Epstein-Barr virus (EBV), are members of the gammaherpesvirus subfamily, a group of viruses whose infection is associated with multiple malignancies, including cancer. The primary host for these viruses is humans and, like all herpesviruses, infection with these pathogens is lifelong. Due to the persistence of gammaherpesvirus infection and the potential for cancer formation in infected individuals, there is a driving need to understand not only the biology of these viruses and how they remain undetected in host cells but also the mechanism(s) by which tumorigenesis occurs. One of the methods that has provided much insight into these processes is proteomics. Proteomics is the study of all the proteins that are encoded by a genome and allows for (i) identification of existing and novel proteins derived from a given genome, (ii) interrogation of protein-protein interactions within a system, and (iii) discovery of druggable targets for the treatment of malignancies. In this chapter, we explore how proteomics has contributed to our current understanding of gammaherpesvirus biology and their oncogenic processes, as well as the clinical applications of proteomics for the detection and treatment of gammaherpesvirus-associated cancers.
DNA 病毒,卡波济肉瘤相关疱疹病毒(KSHV)和 Epstein-Barr 病毒(EBV),是γ疱疹病毒亚科的成员,该病毒亚科的一组病毒感染与多种恶性肿瘤有关,包括癌症。这些病毒的主要宿主是人类,与所有疱疹病毒一样,这些病原体的感染是终身的。由于γ疱疹病毒感染的持续存在以及感染个体中癌症形成的潜在风险,人们迫切需要了解这些病毒的生物学特性以及它们在宿主细胞中如何保持未被检测到,还需要了解肿瘤发生的机制。蛋白质组学是一种提供了对这些过程的深入了解的方法之一。蛋白质组学是对由基因组编码的所有蛋白质的研究,它允许(i)鉴定来自给定基因组的现有和新的蛋白质,(ii)在系统内检测蛋白质-蛋白质相互作用,以及(iii)发现可用于治疗恶性肿瘤的可用药靶。在本章中,我们探讨了蛋白质组学如何促进我们对γ疱疹病毒生物学及其致癌过程的现有理解,以及蛋白质组学在检测和治疗γ疱疹病毒相关癌症方面的临床应用。