Journal
ONCOGENE
Volume 24, Issue 55, Pages 8154-8166Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.onc.1208986
Keywords
HIF-1; VEGF; angiogenesis; hypoxia; MnSOD
Funding
- NCI NIH HHS [CA66081, CA81090] Funding Source: Medline
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Hypoxia-inducible factor-1 (HIF-1) is a transcription factor that governs cellular responses to reduced O-2 availability by mediating crucial homeostatic processes. HIF-1 is composed of an HIF-1 alpha subunit and an HIF-1 beta subunit. HIF-1 alpha is degraded following enzyme-dependent hydroxylation of prolines of HIF-1 alpha in the presence of molecular oxygen, Fe2+, alpha-ketoglutarate, and ascorbate. These cofactors contribute to the redox environment of cells. The antioxidant enzyme manganese superoxide dismutase (MnSOD) also modulates the cellular redox environment. Here we show that MnSOD suppressed hypoxic accumulation of HIF-1 alpha protein in human breast carcinoma MCF-7 cells. This suppression was biphasic depending on MnSOD activity. At low levels of MnSOD activity, HIF-1 alpha protein accumulated under hypoxic conditions. At moderate levels of MnSOD activity (two-to six-fold increase compared to parent cells), these accumulations were blocked. However, at higher levels of MnSOD activity (> 6-fold increase), accumulation of HIF-1 alpha protein was again observed. This biphasic modulation was observed under both 1 and 4% O-2. Coexpression of mitochondrial hydrogen peroxide-removing proteins prevented the accumulation of HIF-1 alpha protein in cells with high levels of MnSOD; this effect demonstrates that the restabilization of HIF-1 alpha observed in high MnSOD overexpressors is probably due to hydrogen peroxide, most likely produced from MnSOD. Hypoxic induction of vascular endothelial growth factor ( VEGF) protein was also suppressed by elevated MnSOD activity and its levels reflected HIF-1 alpha protein levels. These observations demonstrated that HIF-1 alpha accumulation and VEGF expression could be modulated by the antioxidant enzyme MnSOD.
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