Expression of hypoxia inducible factor-1α in HepG2 cells cultured under hypoxia and its relationship with vascularization and apoptosis-related protein
- Author:
Zhi-Cao FU
1
Author Information
1. Department of Radiotherapy
- Publication Type:Journal Article
- Keywords:
bcl-2;
Caspases;
Genes;
Hypoxia inducible factor-1α;
Liver neoplasmas;
Vascular endothelial growth factors
- From:
Academic Journal of Second Military Medical University
2010;27(12):1328-1332
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To investigate the expression of hypoxia inducible factor-1α(HIF-1α) in HepG2 cells cultured under hypoxia for different time periods, and to assess its relationship with vascularization and cell apoptosis. Methods: HepG2 cells were cultured in a medium containing cobalt chloride (125 μmol/L) for different time periods (0, 1, 2, 4, 6, and 8 hours). RT-PCR was used to measure the expression of HIF-1α mRNA, VEGF mRNA, and bcl-2 mRNA, and bax mRNA at the above time points; Western blot was used to determine the expression of Caspase-3 protein and the activity of Caspase 3 enzyme. Results: After 1-2 hour culture under hypoxia, the expression of HIF-1α mRNA, VEGF mRNA, and bcl-2 mRNA began to increase gradually, peaked at 4 h, and then decreased, but were still higher than that before culture. There was no obvious change in the expression of bax mRNA and the ratio of bcl-2 to bax mRNA expression had a similar change with that of bcl-2 mRNA expression. The changes of Caspase-3 protein/mRNA and Caspase-3 enzyme activity were contrary to that of HIF-1α. Conclusion: HIF-1α may inhibit the apoptosis of hepatic cancer cells through regulating the expression of VEGF, bcl-2, bax, and Caspase-3, and the inhibition is related to the severity of hypoxia.
