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ZBP-89 enhances Bak expression and causes apoptosis in hepatocellular carcinoma cells.
- Source :
-
Biochimica et biophysica acta [Biochim Biophys Acta] 2011 Jan; Vol. 1813 (1), pp. 222-30. Date of Electronic Publication: 2010 Sep 17. - Publication Year :
- 2011
-
Abstract
- ZBP-89 can enhance tumor cells to death stimuli. However, the molecular mechanism leading to the inhibitory effect of ZBP-89 is unknown. In this study, 4 liver cell lines were used to screen for the target of ZBP-89 on cell death pathway. The identified Bak was further analyzed for its role in ZBP-89-mediated apoptosis. The result showed that ZBP-89 significantly and time-dependently induced apoptosis. It significantly upregulated the level of pro-apoptotic Bak. ZBP-89 targeted a region between -457 and -407 of human Bak promoter to stimulate Bak expression based on the findings of Bak promoter luciferase report gene assay and electrophoretic mobility shift assay. ZBP-89-induced Bak increase and ZBP-89-mediated apoptosis were markedly suppressed by Bak siRNA, confirming that Bak was specifically targeted by ZBP-89 to facilitate apoptosis. In conclusion, this study demonstrated that ZBP-89 significantly induced apoptosis of HCC cells via promoting Bak level.<br /> (Copyright © 2010 Elsevier B.V. All rights reserved.)
- Subjects :
- Blotting, Western
Carcinoma, Hepatocellular genetics
Carcinoma, Hepatocellular metabolism
Cell Proliferation
DNA-Binding Proteins genetics
Electrophoretic Mobility Shift Assay
Humans
Liver Neoplasms genetics
Liver Neoplasms metabolism
Luciferases metabolism
Promoter Regions, Genetic genetics
RNA, Small Interfering genetics
Transcription Factors genetics
Tumor Cells, Cultured
bcl-2 Homologous Antagonist-Killer Protein antagonists & inhibitors
bcl-2 Homologous Antagonist-Killer Protein metabolism
Apoptosis
Carcinoma, Hepatocellular pathology
DNA-Binding Proteins metabolism
Liver Neoplasms pathology
Transcription Factors metabolism
bcl-2 Homologous Antagonist-Killer Protein genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0006-3002
- Volume :
- 1813
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Biochimica et biophysica acta
- Publication Type :
- Academic Journal
- Accession number :
- 20850481
- Full Text :
- https://doi.org/10.1016/j.bbamcr.2010.09.005