Characterization of Epstein-Barr virus gp350/220 gene variants in virus isolates from gastric carcinoma and nasopharyngeal carcinoma

Bing Luo; Mengyang Liu; Yan Chao; Yun Wang; Yongzheng Jing; Zhifu Sun

doi:10.1007/s00705-011-1148-z

Characterization of Epstein-Barr virus gp350/220 gene variants in virus isolates from gastric carcinoma and nasopharyngeal carcinoma

Bing Luo, Mengyang Liu, Yan Chao, Yun Wang, Yongzheng Jing, Zhifu Sun

Quantitative Health Sciences

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Abstract

To characterize the sequence variation of the gp350/220 and explore its potential association with EBV-associated tumors, the gp350/220 gene was sequenced from 41 EBV-associated gastric carcinoma (EBVaGC) and 81 nasopharyngeal carcinoma (NPC) biopsies as well as 35 throat washing (TW) samples from healthy donors. Preferential linkages between variants of the N-terminus of gp350/220 and EBNA3C variants were detected, and type A/BLLF1-a was the dominant variant in this study. The dominant variant in the C-terminal region of gp350/220 was 9P. The similar distribution of gp350/220 variants in NPC, EBVaGC and healthy donors suggest that gp350/220 variations are geographically restricted rather than tumor-specific polymorphisms.

Original language	English (US)
Pages (from-to)	207-216
Number of pages	10
Journal	Archives of Virology
Volume	157
Issue number	2
DOIs	https://doi.org/10.1007/s00705-011-1148-z
State	Published - Feb 2012

ASJC Scopus subject areas

Virology

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title = "Characterization of Epstein-Barr virus gp350/220 gene variants in virus isolates from gastric carcinoma and nasopharyngeal carcinoma",

abstract = "To characterize the sequence variation of the gp350/220 and explore its potential association with EBV-associated tumors, the gp350/220 gene was sequenced from 41 EBV-associated gastric carcinoma (EBVaGC) and 81 nasopharyngeal carcinoma (NPC) biopsies as well as 35 throat washing (TW) samples from healthy donors. Preferential linkages between variants of the N-terminus of gp350/220 and EBNA3C variants were detected, and type A/BLLF1-a was the dominant variant in this study. The dominant variant in the C-terminal region of gp350/220 was 9P. The similar distribution of gp350/220 variants in NPC, EBVaGC and healthy donors suggest that gp350/220 variations are geographically restricted rather than tumor-specific polymorphisms.",

author = "Bing Luo and Mengyang Liu and Yan Chao and Yun Wang and Yongzheng Jing and Zhifu Sun",

note = "Funding Information: This research was supported by a grant from the National Natural Science Foundation of China (NSFC 30740068 and NSFC30471623); the Natural Science Foundation of Shandong Province, China (Y2008C90); and Science and Technology of Qingdao City, China (08-2-3-7-hz and 08-2-1-4-nsh).",

year = "2012",

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doi = "10.1007/s00705-011-1148-z",

language = "English (US)",

volume = "157",

pages = "207--216",

journal = "Archives of Virology",

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T1 - Characterization of Epstein-Barr virus gp350/220 gene variants in virus isolates from gastric carcinoma and nasopharyngeal carcinoma

AU - Luo, Bing

AU - Liu, Mengyang

AU - Chao, Yan

AU - Wang, Yun

AU - Jing, Yongzheng

AU - Sun, Zhifu

N1 - Funding Information: This research was supported by a grant from the National Natural Science Foundation of China (NSFC 30740068 and NSFC30471623); the Natural Science Foundation of Shandong Province, China (Y2008C90); and Science and Technology of Qingdao City, China (08-2-3-7-hz and 08-2-1-4-nsh).

PY - 2012/2

Y1 - 2012/2

N2 - To characterize the sequence variation of the gp350/220 and explore its potential association with EBV-associated tumors, the gp350/220 gene was sequenced from 41 EBV-associated gastric carcinoma (EBVaGC) and 81 nasopharyngeal carcinoma (NPC) biopsies as well as 35 throat washing (TW) samples from healthy donors. Preferential linkages between variants of the N-terminus of gp350/220 and EBNA3C variants were detected, and type A/BLLF1-a was the dominant variant in this study. The dominant variant in the C-terminal region of gp350/220 was 9P. The similar distribution of gp350/220 variants in NPC, EBVaGC and healthy donors suggest that gp350/220 variations are geographically restricted rather than tumor-specific polymorphisms.

AB - To characterize the sequence variation of the gp350/220 and explore its potential association with EBV-associated tumors, the gp350/220 gene was sequenced from 41 EBV-associated gastric carcinoma (EBVaGC) and 81 nasopharyngeal carcinoma (NPC) biopsies as well as 35 throat washing (TW) samples from healthy donors. Preferential linkages between variants of the N-terminus of gp350/220 and EBNA3C variants were detected, and type A/BLLF1-a was the dominant variant in this study. The dominant variant in the C-terminal region of gp350/220 was 9P. The similar distribution of gp350/220 variants in NPC, EBVaGC and healthy donors suggest that gp350/220 variations are geographically restricted rather than tumor-specific polymorphisms.

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Characterization of Epstein-Barr virus gp350/220 gene variants in virus isolates from gastric carcinoma and nasopharyngeal carcinoma

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