A Systematic Review of Epstein-Barr Virus Latent Membrane Protein 1 (LMP1) Gene Variants in Nasopharyngeal Carcinoma

被引:8
|
作者
Banko, Ana [1 ]
Miljanovic, Danijela [1 ]
Lazarevic, Ivana [1 ]
Cirkovic, Andja [2 ]
机构
[1] Univ Belgrade, Inst Microbiol & Immunol, Fac Med, Belgrade 11000, Serbia
[2] Univ Belgrade, Inst Med Stat & Informat, Fac Med, Belgrade 11000, Serbia
来源
PATHOGENS | 2021年 / 10卷 / 08期
关键词
EBV; nasopharyngeal carcinoma; LMP1; gene variability; variants; meta-analysis; 30-BP DELETION VARIANT; ORAL-CAVITY TUMORS; AMINO-ACID CHANGES; T-CELL-LYMPHOMA; SEQUENCE VARIATION; HODGKINS-DISEASE; HIGH-FREQUENCY; NECK TUMORS; BP DELETION; PREVALENCE;
D O I
10.3390/pathogens10081057
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Nasopharyngeal carcinoma (NPC) is an aggressive tumor with a complex etiology. Although Epstein-Barr virus (EBV) infection is known environmental factor for NPC development, the degree to which EBV naturally infects nasopharyngeal epithelium and the moment when and why the virus actively begins to affect cell transformation remains questionable. The aim of this study was to explore the association between LMP1 gene variability and potential contribution to NPC development. A systematic review was performed through searches of PubMed, Web of Science (WoS) and SCOPUS electronic databases. Additionally, meta-analysis of the difference in the frequency of seven LMP1 gene variants in NPC and control individuals was accomplished. The results from this study give a proof of concept for the association between 30 bp deletion (OR = 3.53, 95% CI = 1.48-8.43) and Xhol loss (OR = 14.17, 95% CI = 4.99-40.20) and NPC susceptibility when comparing biopsies from NPC and healthy individuals. Otherwise, 30 bp deletion from NPC biopsies could not distinguish NPC from EBV-associated non-NPC tumors (OR = 1.74, 95% CI = 0.81-3.75). However, B95-8, China1 and North Carolina variants were uncommon for NPC individuals. Much more efforts remains to be done to verify the biological significance of the differences observed, define so-called "high-risk" EBV variants and make it available for clinical application.
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页数:31
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