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乙型肝炎病毒X蛋白对原癌基因c-jun的激活作用。

Activation of protooncogene c-jun by the X protein of hepatitis B virus.

作者信息

Twu J S, Lai M Y, Chen D S, Robinson W S

机构信息

Department of Medicine, Stanford University School of Medicine, California 94305.

出版信息

Virology. 1993 Jan;192(1):346-50. doi: 10.1006/viro.1993.1041.

Abstract

A specific viral oncogenic mechanism has not been shown for hepatitis B virus (HBV), although persistent HBV infection has been strongly associated with the development of hepatocellular carcinoma (HCC). Most HCCs in HBV carriers contain integrated viral sequences in host DNA and this raises the question of whether such integrations ever contribute to oncogenesis. HBV does contain a gene (designated the hbx gene) which encodes a transcriptional trans-activator protein capable of activating homologous and heterologous regulatory sequences. Hbx has been detected in some human HCC with HBV integrations and the expressed hbx protein appears to have transcriptional transactivating activity. These findings raise the possibility that hbx expression could contribute to hepatocarcinogenesis by activating cellular genes that could contribute to oncogenicity. The possibility that the hbx protein may activate certain protooncogenes was investigated and we found that hbx can activate the protooncogene c-jun promoter. c-Jun was found to be expressed at a very low level in normal liver tissue but at high levels in HCCs of HBV-infected patients.

摘要

尽管乙型肝炎病毒(HBV)持续感染与肝细胞癌(HCC)的发生密切相关,但尚未发现HBV具体的病毒致癌机制。HBV携带者中的大多数HCC含有整合到宿主DNA中的病毒序列,这就引发了一个问题,即这种整合是否对肿瘤发生有作用。HBV确实含有一个基因(称为hbx基因),该基因编码一种转录反式激活蛋白,能够激活同源和异源调控序列。在一些伴有HBV整合的人类HCC中检测到了Hbx,并且所表达的hbx蛋白似乎具有转录反式激活活性。这些发现增加了一种可能性,即hbx表达可能通过激活可能导致致癌性的细胞基因而促进肝癌发生。研究了hbx蛋白可能激活某些原癌基因的可能性,我们发现hbx可以激活原癌基因c-jun启动子。发现c-Jun在正常肝组织中表达水平非常低,但在HBV感染患者的HCC中表达水平很高。

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