Ethnic differences in the expression of Epstein-Barr virus latent membrane protein-1 mutations in nasopharyngeal carcinoma

被引:17
作者
D'Addario, M [1 ]
Chauvin, P [1 ]
机构
[1] McGill Univ, Montreal Gen Hosp, Fac Dent, Dept Pathol, Montreal, PQ H3G 1A4, Canada
关键词
Epstein-Barr virus; nasopharyngeal carcinoma; latent membrane protein;
D O I
10.1016/S0027-5107(00)00129-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The latent membrane protein-1 (LMP1) of Epstein-Barr virus (EBV) is a viral oncoprotein implicated in several EBV-associated pathologies. Many studies have characterized carboxy-terminal mutations within LMP1, errors in this area are critical since this portion contains sequences responsible for LMP1 targeting, half-life and association with host cell proteins. Although, data suggests that mutations in this area extend LMP1 half-life and increase its oncogenesis, some studies have not shown this to be true for all EBV-associated tumors. In order to evaluate 3'-end LMP1-DNA mutations in three different ethnic populations with nasopharyngeal carcinoma (NPC), we examined EBV-DNA in 34 patients of various origins (Caucasian, Chinese and Inuit). While 68% of the total group expressed EBV-antigens, only 56% of Caucasians but 86% of Inuit expressed this viral protein. Over 67% of Inuit NPC tissue contained the characteristic 30 bp deletion that was observed in only 20% of Caucasians and 33% of Chinese samples. DNA sequencing revealed that the Inuit population showed the most frequent DNA mutations and corresponding amino acid alterations in LMP1. Our results suggest that EBV-associated NPC-DNA mutations in LMP1 do not occur at equal rates in different racial groups and are more common at distinct sites in NPC tissue from Chinese and Inuit sources. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:69 / 78
页数:10
相关论文
共 43 条
[1]  
BAICHWAL VR, 1988, ONCOGENE, V2, P461
[2]   The NF-kappa B and I kappa B proteins: New discoveries and insights [J].
Baldwin, AS .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :649-683
[3]   The 30-bp deletion variant of Epstein-Barr virus-encoded latent membrane protein-1 prevails in acute infectious mononucleosis [J].
Berger, C ;
McQuain, C ;
Sullivan, JL ;
Nadal, D ;
Quesenberry, PJ ;
Knecht, H .
JOURNAL OF INFECTIOUS DISEASES, 1997, 176 (05) :1370-1373
[4]   Localization of the major NF-kappa B-activating site and the sole TRAF3 binding site of LMP-1 defines two distinct signaling motifs [J].
Brodeur, SR ;
Cheng, GH ;
Baltimore, D ;
ThorleyLawson, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (32) :19777-19784
[5]  
CHEN ML, 1992, ONCOGENE, V7, P2131
[6]  
Cheung ST, 1999, INT J CANCER, V83, P121, DOI 10.1002/(SICI)1097-0215(19990924)83:1<121::AID-IJC21>3.0.CO
[7]  
2-F
[8]   Epstein-Barr virus strains with latent membrane protein-1 deletions: Prevalence in the Italian population and high association with human immunodeficiency virus-related Hodgkin's disease [J].
Dolcetti, R ;
Zancai, P ;
De Re, V ;
Gloghini, A ;
Bigoni, B ;
Pivetta, B ;
DeVita, S ;
Carbone, A ;
Boiocchi, M .
BLOOD, 1997, 89 (05) :1723-1731
[9]  
Essop MF, 1999, INT J CANCER, V84, P449, DOI 10.1002/(SICI)1097-0215(19990820)84:4&lt
[10]  
449::AID-IJC21&gt