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[Cancer Research 66, 9099-9107, September 15, 2006]
© 2006 American Association for Cancer Research


Cell, Tumor, and Stem Cell Biology

HBXIP, Cellular Target of Hepatitis B Virus Oncoprotein, Is a Regulator of Centrosome Dynamics and Cytokinesis

Ryoji Fujii1, Changjun Zhu1, Yunfei Wen1, Hiroyuki Marusawa1, Beatrice Bailly-Maitre1, Shu-ichi Matsuzawa1, Hong Zhang2, Youngsoo Kim2, C. Frank Bennett2, Wei Jiang1 and John C. Reed1

1 Burnham Institute for Medical Research, La Jolla, California and 2 ISIS Pharmaceuticals, Inc., Carlsbad, California

Requests for reprints: John C. Reed, Burnham Institute for Medical Research, 10904 North Torrey Pines Road, La Jolla, CA 92037. Phone: 858-646-5301; Fax: 858-646-3194; E-mail: reedoffice{at}burnham.org.

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. (Cancer Res 2006; 66(18): 9099-107)




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Y. Wen, V. S. Golubkov, A. Y. Strongin, W. Jiang, and J. C. Reed
Interaction of Hepatitis B Viral Oncoprotein with Cellular Target HBXIP Dysregulates Centrosome Dynamics and Mitotic Spindle Formation
J. Biol. Chem., February 1, 2008; 283(5): 2793 - 2803.
[Abstract] [Full Text] [PDF]




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Copyright © 2006 by the American Association for Cancer Research.