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Hepatitis B virus pathogenesis: Fresh insights into hepatitis B virus RNA
被引:15
|作者:
Sekiba, Kazuma
[1
]
Otsuka, Motoyuki
[1
]
Ohno, Motoko
[1
]
Yamagami, Mari
[1
]
Kishikawa, Takahiro
[1
]
Suzuki, Tatsunori
[1
]
Ishibashi, Rei
[1
]
Seimiya, Takahiro
[1
]
Tanaka, Eri
[1
]
Koike, Kazuhiko
[1
]
机构:
[1] Univ Tokyo, Grad Sch Med, Dept Gastroenterol, Tokyo 1138655, Japan
关键词:
Hepatitis B virus;
Hepatitis B virus RNA;
MicroRNA;
Smc5/6;
Viral replication;
Hepatic fibrosis;
Genome integration;
Hepatocellular carcinoma;
CLOSED CIRCULAR DNA;
HEPATOCELLULAR-CARCINOMA;
GENE-EXPRESSION;
MESSENGER-RNA;
AUSTRALIA-ANTIGEN;
TUMOR-SUPPRESSOR;
DOWN-REGULATION;
LIVER FIBROSIS;
HOST MICRORNA;
IN-VIVO;
D O I:
10.3748/wjg.v24.i21.2261
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Hepatitis B virus (HBV) is still a worldwide health concern. While divergent factors are involved in its pathogenesis, it is now clear that HBV RNAs, principally templates for viral proteins and viral DNAs, have diverse biological functions involved in HBV pathogenesis. These functions include viral replication, hepatic fibrosis and hepatocarcinogenesis. Depending on the sequence similarities, HBV RNAs may act as sponges for host miRNAs and may deregulate miRNA functions, possibly leading to pathological consequences. Some parts of the HBV RNA molecule may function as viral-derived miRNA, which regulates viral replication. HBV DNA can integrate into the host genomic DNA and produce novel viral-host fusion RNA, which may have pathological functions. To date, elimination of HBV-derived covalently closed circular DNA has not been achieved. However, RNA transcription silencing may be an alternative practical approach to treat HBV-induced pathogenesis. A full understanding of HBV RNA transcription and the biological functions of HBV RNA may open a new avenue for the development of novel HBV therapeutics.
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页码:2261 / 2268
页数:8
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