Negative regulation of HIF-1α by an FBW7-mediated degradation pathway during hypoxia

✍ Scribed by Jessica M. Cassavaugh; Sarah A. Hale; Theresa L. Wellman; Alan K. Howe; Cheung Wong; Karen M. Lounsbury

• Publisher: John Wiley and Sons
• Year: 2011
• Tongue: English
• Weight: 470 KB
• Volume: 112
• Category: Article
• ISSN: 0730-2312
• DOI: 10.1002/jcb.23321

✦ Synopsis

Hypoxia inducible factor-1a (HIF-1a) stimulates expression of genes associated with angiogenesis and is associated with poor outcomes in ovarian and other cancers. In normoxia, HIF-1a is ubiquitinated and degraded through the E3 ubiquitin ligase, von Hippel-Lindau; however, little is known about the regulation of HIF-1a in hypoxic conditions. FBW7 is an E3 ubiquitin ligase that recognizes proteins phosphorylated by glycogen synthase kinase 3b (GSK3b) and targets them for destruction. This study used an ovarian cancer cell model to test the hypothesis that HIF-1a phosphorylation by GSK3b in hypoxia leads to interaction with FBW7 and ubiquitin-dependent degradation. Expression of constitutively active GSK3b reduced HIF-1a protein and transcriptional activity and increased ubiquitination of HIF-1a in hypoxia, whereas pharmacologic inhibition of GSK3 or expression of siGSK3b promoted HIF-1a stabilization and activity. A mechanism through FBW7 was supported by the observed decrease in HIF-1a stabilization when FBW7 was overexpressed and both the elevation of HIF-1a levels and decrease in ubiquitinated HIF-1a when FBW7 was suppressed. Furthermore, HIF-1a associated with FBW7g 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 GSK3b or FBW7. These data introduce a new mechanism for regulation of HIF-1a during hypoxia that utilizes phosphorylation to target HIF-1a for ubiquitin-dependent degradation through FBW7 and may identify new targets in the regulation of angiogenesis.