Viral-Targeted Strategies Against EBV-Associated Lymphoproliferative Diseases

被引:20
作者
Hui, Kwai Fung [1 ]
Yiu, Stephanie Pei Tung [1 ]
Tam, Kam Pui [1 ]
Chiang, Alan Kwok Shing [1 ,2 ]
机构
[1] Univ Hong Kong, Queen Mary Hosp, Li Ka Shing Fac Med, Dept Paediat & Adolescent Med, Hong Kong, Peoples R China
[2] Univ Hong Kong, Ctr Nasopharyngeal Carcinoma Res, Hong Kong, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2019年 / 9卷
关键词
Epstein-Barr virus; lymphoproliferative diseases; viral-targeted strategies; EBV latency; lytic cycle reactivation; histone deacetylase inhibitors; proteasome inhibitors; EPSTEIN-BARR-VIRUS; NUCLEAR ANTIGEN 3C; B-CELL PROLIFERATION; NATURAL-KILLER-CELLS; CD8(+) T-CELLS; LYTIC CYCLE; LATENT MEMBRANE-PROTEIN-1; NASOPHARYNGEAL CARCINOMA; INCREASED RESISTANCE; GENOMIC INSTABILITY;
D O I
10.3389/fonc.2019.00081
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epstein-Barr virus (EBV) is strongly associated with a spectrum of EBV-associated lymphoproliferative diseases (EBV-LPDs) ranging from post-transplant lymphoproliferative disorder, B cell lymphomas (e.g., endemic Burkitt lymphoma, Hodgkin lymphoma, and diffuse large B cell lymphoma) to NK or T cell lymphoma (e.g., nasal NK/T-cell lymphoma). The virus expresses a number of latent viral proteins which are able to manipulate cell cycle and cell death processes to promote survival of the tumor cells. Several FDA-approved drugs or novel compounds have been shown to induce killing of some of the EBV-LPDs by inhibiting the function of latent viral proteins or activating the viral lytic cycle from latency. Here, we aim to provide an overview on the mechanisms by which EBV employs to drive the pathogenesis of various EBV-LPDs and to maintain the survival of the tumor cells followed by a discussion on the development of viral-targeted strategies based on the understanding of the patho-mechanisms.
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页数:18
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