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Identification and extensive analysis of inverted-duplicated HBV integration in a human hepatocellular carcinoma cell line
被引:4
|作者:
Bok, Jeong
[1
]
Kim, Kwang Joong
[1
]
Park, Mi-Hyun
[1
]
Cho, Seung-Hak
[2
]
Lee, Hye-Ja
[1
]
Lee, Eun-Ju
[1
]
Park, Chan
[1
]
Lee, Jong-Young
[1
]
机构:
[1] Natl Inst Hlth, Ctr Genome Sci, Div Struct & Funct Genom, Chungcheongbuk Do 363951, South Korea
[2] Natl Inst Hlth, Ctr Infect Dis, Div Enter Bacterial Infect, Chungcheongbuk Do 363951, South Korea
来源:
关键词:
Chromosome;
11q13;
Hepatitis B virus;
Hepatocellular carcinoma;
Integration;
Rearrangement;
HEPATITIS-B-VIRUS;
DNA INTEGRATION;
INSERTIONAL MUTAGENESIS;
GENE;
EXPRESSION;
CANCER;
AMPLIFICATION;
FIBROBLAST-GROWTH-FACTOR-19;
OVEREXPRESSION;
PATHOGENESIS;
D O I:
10.5483/BMBRep.2012.45.6.279
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Hepatitis B virus (HBV) DNA is often integrated into hepatocellular carcinoma (HCC). Although the relationship between HBV integration and HCC development has been widely studied, the role of HBV integration in HCC development is still not completely understood. In the present study, we constructed a pooled BAC library of 9 established cell lines derived from HCC patients with HBV infections. By amplifying viral genes and superpooling of BAC clones, we identified 2 clones harboring integrated HBV DNA. Screening of host-virus junctions by repeated sequencing revealed an HBV DNA integration site on chromosome 11q13 in the SNU-886 cell line. The structure and rearrangement of integrated HBV DNA were extensively analyzed. An inverted duplicated structure, with fusion of at least 2 HBV DNA molecules in opposite orientations, was identified in the region. The gene expression of cancer-related genes increased near the viral integration site in HCC cell line SNU-886. [BMB Reports 2012; 45(6): 365-370]
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页码:365 / 370
页数:6
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