Negative Regulation of HIF-1α by an FBW7-Mediated Degradation Pathway During Hypoxia

Hypoxia inducible factor-1 alpha (HIF-1 alpha) stimulates expression of genes associated with angiogenesis and is associated with poor outcomes in ovarian and other cancers. In normoxia, HIF-1 alpha is ubiquitinated and degraded through the E3 ubiquitin ligase, von Hippel-Lindau; however, little is known about the regulation of HIF-1 alpha in hypoxic conditions. FBW7 is an E3 ubiquitin ligase that recognizes proteins phosphorylated by glycogen synthase kinase 3 beta (GSK3 beta) and targets them for destruction. This study used an ovarian cancer cell model to test the hypothesis that HIF-1 alpha phosphorylation by GSK3 beta in hypoxia leads to interaction with FBW7 and ubiquitin-dependent degradation. Expression of constitutively active GSK3 beta reduced HIF-1 alpha protein and transcriptional activity and increased ubiquitination of HIF-1 alpha in hypoxia, whereas pharmacologic inhibition of GSK3 or expression of siGSK3 beta promoted HIF-1a stabilization and activity. A mechanism through FBW7 was supported by the observed decrease in HIF-1 alpha stabilization when FBW7 was overexpressed and both the elevation of HIF-1 alpha levels and decrease in ubiquitinated HIF-1 alpha when FBW7 was suppressed. Furthermore, HIF-1a associated with FBW7 gamma by co-immunoprecipitation, and the interaction was weakened by inhibition of GSK3 or mutation of GSK3b phosphorylation sites. The relevance of this pathway to angiogenic signaling was supported by the finding that endothelial cell tube maturation was increased by conditioned media from hypoxic SK-OV-3 cell lines expressing suppressed GSK3 beta or FBW7. These data introduce a new mechanism for regulation of HIF-1 alpha during hypoxia that utilizes phosphorylation to target HIF-1 alpha for ubiquitin-dependent degradation through FBW7 and may identify new targets in the regulation of angiogenesis. J. Cell. Biochem. 112: 3882-3890, 2011. (C) 2011 Wiley Periodicals, Inc.