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EMBO J. 2003 Jun 2;22(11):2729-40.

HBXIP functions as a cofactor of survivin in apoptosis suppression.

Author information

  • 1The Burnham Institute, La Jolla, CA 92037, USA.

Abstract

Survivin is an anti-apoptotic protein that is overexpressed in most human cancers. We show that survivin forms complexes with a cellular protein, hepatitis B X-interacting protein (HBXIP), which was originally recognized for its association with the X protein of hepatitis B virus (HBX). Survivin-HBXIP complexes, but neither survivin nor HBXIP individually, bind pro-caspase-9, preventing its recruitment to Apaf1, and thereby selectively suppressing apoptosis initiated via the mitochondria/cytochrome c pathway. Viral HBX protein also interacts with the survivin- HBXIP complex and suppresses caspase activation in a survivin-dependent manner. Thus, HBXIP functions as a cofactor for survivin, and serves as a link between the cellular apoptosis machinery and a viral pathogen involved in hepatocellular carcinogenesis.

PMID:
12773388
[PubMed - indexed for MEDLINE]
PMCID:
PMC156760
Free PMC Article

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