Hepatitis B virus promotes hepatocarcinogenesis in transgenic mice

被引:74
|
作者
Zheng, Yanyan
Chen, Wen-ling
Louie, Stan G.
Yen, T. S. Benedict
Ou, Jing-hsiung James
机构
[1] Univ So Calif, Keck Sch Med, Dept Mol Microbiol & Immunol, Los Angeles, CA 90033 USA
[2] Univ So Calif, Dept Pharm, Los Angeles, CA 90033 USA
[3] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
[4] Vet Adm Med Ctr, Pathol Serv, San Francisco, CA 94121 USA
关键词
D O I
10.1002/hep.21445
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
HBV is a major risk factor for hepatocellular carcinoma (HCC). However, whether HBV can directly cause HCC or only indirectly via the induction of chronic liver inflammation has been controversial. By using transgenic mice carrying the entire HBV genome as a model, we now demonstrate that HBV by itself is an inefficient carcinogen. However, it can efficiently promote hepatocarcinogenesis initiated by the carcinogen diethylnitrosamine (DEN). This effect of HBV does not involve chronic liver inflammation, is apparently due to enhanced hepatocellular apoptosis and compensatory regeneration following DEN treatment, and does not require the HBV X protein. Conclusion: Our results demonstrate a direct role of HBV in a hepatocarcinogenesis pathway that involves the interaction between this virus and a dietary carcinogen.
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页码:16 / 21
页数:6
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