cDNA Expression Array Analysis of Gene Expression in Human Hepatocarcinoma Hep3B Cells Induced By BNIPL-1
Article first published online: 27 SEP 2005
DOI: 10.1111/j.1745-7270.2005.00086.x
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How to Cite
XIE, L., QIN, W.-X., LI, J.-J., HE, X.-H., SHU, H.-Q., YAO, G.-F., WAN, D.-F. and GU, J.-R. (2005), cDNA Expression Array Analysis of Gene Expression in Human Hepatocarcinoma Hep3B Cells Induced By BNIPL-1. Acta Biochimica et Biophysica Sinica, 37: 618–624. doi: 10.1111/j.1745-7270.2005.00086.x
Publication History
- Issue published online: 27 SEP 2005
- Article first published online: 27 SEP 2005
- Received: May 9, 2005 Accepted: June 14, 2005
- Abstract
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Keywords:
- BNIPL-1;
- Tet-on;
- Atlas human cDNA array;
- apoptosis
Abstract Bcl-2/adenovirus E1B 19 kDa interacting protein 2 like-1 (BNIPL-1) is a novel human protein identified in our laboratory, which can interact with Bc1-2 and Cdc42GAP and induce apoptosis via the BNIP-2 and Cdc42GAP homology (BCH) domain. In the present study, we established the Hep3B-Tet-on stable cell line in which expression of BNIPL-1 can be induced by doxycycline. The cell proliferation activity assay showed that the overexpression of BNIPL-1 suppresses Hep3B cell growth in vitro. The differential expression profiles of 588 known genes from BNIPL-1-transfected Hep3B-Tet-on and vector control cells were determined using the Atlas human cDNA expression array. Fifteen genes were differentially expressed between these two cell lines, among which seven genes were up-regulated and eight genes were down-regulated by BINPL-1. Furthermore, the differential expression result was confirmed by semiquantitative RT-PCR. Among these differentially expressed genes, p16INK4, IL-12, TRAIL and the lymphotoxin β gene involved in growth suppression or cell apoptosis were up-regulated, and PTEN involved in cell proliferation was down-regulated by BNIPL-1. These results suggest that BNIPL-1 might inhibit cell growth though cell cycle arrest and/or apoptotic cell death pathway(s).
Edited by Ding-Gan LIU

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