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HBXIP, cellular target of hepatitis B virus oncoprotein, is a regulator of centrosome dynamics and cytokinesis.

HBXIP, cellular target of hepatitis B virus oncoprotein, is a regulator of centrosome dynamics and cytokinesis. Research Abstract Details 

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  • HBXIP, cellular target of hepatitis B virus oncoprotein, is a regulator of centrosome dynamics and cytokinesis. Abstract Text:

    ryoji fujiiRyoji Fujii,changjun zhuChangjun Zhu,yunfei wenYunfei Wen,hiroyuki marusawaHiroyuki Marusawa,beatrice bailly-maitreBeatrice Bailly-Maitre,shu-ichi matsuzawaShu-ichi Matsuzawa,hong zhangHong Zhang,youngsoo kimYoungsoo Kim,c frank bennettC Frank Bennett,wei jiangWei Jiang,john c reedJohn C Reed,

    Hepatitis B virus accounts for more than 1 million cancer deaths annually, but the mechanism by which this virus promotes hepatocellular carcinoma remains unclear. The hepatitis B virus genome encodes an oncoprotein, HBx, which binds various cellular proteins including HBXIP. We show here that HBXIP is a regulator of centrosome duplication, required for bipolar spindle formation in HeLa human carcinoma cells and primary mouse embryonic fibroblast cells. We found that most cells deficient in HBXIP arrest in prometaphase with monopolar spindles whereas HBXIP overexpression causes tripolar or multipolar spindles due to excessive centrosome replication. Additionally, a defect in cytokinesis was seen in HBXIP-deficient HeLa cells, with most cells failing to complete division and succumbing eventually to apoptosis. Expression of viral HBx in HeLa cells mimicked the effects of HBXIP overexpression, causing excessive centrosome replication, resulting in tripolar and multipolar spindles and defective cytokinesis. Immunolocalization and fluorescent protein tagging experiments showed that HBXIP associates with microtubules of dividing cells and colocalizes with HBx on centrosomes. Thus, viral HBx and its cellular target HBXIP regulate centrosome dynamics and cytokinesis affecting genetic stability. In vivo experiments using antisense oligonucleotides targeting HBXIP in a mouse model of liver regeneration showed a requirement for HBXIP for growth and survival of replicating hepatocytes. Thus, HBXIP is a critical regulator of hepatocyte cell growth in vivo, making it a strong candidate for explaining the tumorigenic actions of viral HBx.

    HBXIP, cellular target of hepatitis B virus oncoprotein, is a regulator of centrosome dynamics and cytokinesis. Publishing Authors By Initials

    r fujiiR Fujii,c zhuC Zhu,y wenY Wen,h marusawaH Marusawa,b bailly-maitreB Bailly-Maitre,s matsuzawaS Matsuzawa,h zhangH Zhang,y kimY Kim,cf bennettCF Bennett,w jiangW Jiang,jc reedJC Reed,

    For similar abstracts research abstracts see: abstracts research

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    HBXIP, cellular target of hepatitis B virus oncoprotein, is a regulator of centrosome dynamics and cytokinesis. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Cancer research

    VOLUME: 66

    Page Numbers: 9099-107

    Journal Abbreviation:

    ISSN: 0008-5472

    DAY: 15

    MONTH: Sep

    YEAR: 2006

    HBXIP, cellular target of hepatitis B virus oncoprotein, is a regulator of centrosome dynamics and cytokinesis. Information

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    LANGUAGE: eng

    NlmUniqueID: 2984705

    HBXIP, cellular target of hepatitis B virus oncoprotein, is a regulator of centrosome dynamics and cytokinesis. Keywords Mesh Terms:

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    Grant and Affiliation Information for HBXIP, cellular target of hepatitis B virus oncoprotein, is a regulator of centrosome dynamics and cytokinesis.

    AFFILIATION: Burnham Institute for Medical Research, La Jolla, California and ISIS Pharmaceuticals, Inc., Carlsbad, California, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Cancer Res

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