Atani Zahra Rafiei, Hosseini Sareh Sadat, Goudarzi Hossein, Faghihloo Ebrahim
Department of Microbiology, Faculty of Medicine, Shahed University, Tehran, Iran.
Student Research Committee, Faculty of Medicine, Shahed University, Tehran, Iran.
Glob Med Genet. 2024 Sep 2;11(4):285-296. doi: 10.1055/s-0044-1790210. eCollection 2024 Dec.
Some human cancers worldwide may be related to human tumor viruses. Knowing, controlling, and managing the viruses that cause cancers remain a problem. Also, tumor viruses use ubiquitin-proteasome system (UPS) that can alter host cellular processes through UPS. Human tumor viruses cause persistent infections, due to their ability to infect their host cells without killing them. Tumor viruses such as Epstein-Barr virus, hepatitis C virus, hepatitis B virus, human papillomaviruses, human T cell leukemia virus, Kaposi's sarcoma-associated herpesvirus, and Merkel cell polyomavirus are associated with human malignancies. They interfere with the regulation of cell cycle and control of apoptosis, which are important for cellular functions. These viral oncoproteins bind directly or indirectly to the components of UPS, modifying cellular pathways and suppressor proteins like p53 and pRb. They can also cause progression of malignancy. In this review, we focused on how viral oncoproteins bind to the components of the UPS and how these interactions induce the degradation of cellular proteins for their survival.
全球范围内,一些人类癌症可能与人类肿瘤病毒有关。了解、控制和管理引发癌症的病毒仍然是一个难题。此外,肿瘤病毒利用泛素 - 蛋白酶体系统(UPS),该系统可通过UPS改变宿主细胞进程。人类肿瘤病毒会引发持续性感染,因为它们能够在不杀死宿主细胞的情况下感染这些细胞。诸如爱泼斯坦 - 巴尔病毒、丙型肝炎病毒、乙型肝炎病毒、人乳头瘤病毒、人类T细胞白血病病毒、卡波西肉瘤相关疱疹病毒和默克尔细胞多瘤病毒等肿瘤病毒与人类恶性肿瘤相关。它们干扰细胞周期调控和细胞凋亡控制,而这对细胞功能至关重要。这些病毒癌蛋白直接或间接与UPS的组分结合,修饰细胞途径以及诸如p53和pRb等抑制蛋白。它们还会导致恶性肿瘤进展。在本综述中,我们重点关注病毒癌蛋白如何与UPS的组分结合,以及这些相互作用如何为其生存诱导细胞蛋白降解。