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

Abstract

Hypoxia inducible factor-1α (HIF-1α) stimulates expression of genes associated with angiogenesis and is associated with poor outcomes in ovarian and other cancers. In normoxia, HIF-1α is ubiquitinated and degraded through the E3 ubiquitin ligase, von Hippel-Lindau; however, little is known about the regulation of HIF-1α in hypoxic conditions. FBW7 is an E3 ubiquitin ligase that recognizes proteins phosphorylated by glycogen synthase kinase 3β (GSK3β) and targets them for destruction. This study used an ovarian cancer cell model to test the hypothesis that HIF-1α phosphorylation by GSK3β in hypoxia leads to interaction with FBW7 and ubiquitin-dependent degradation. Expression of constitutively active GSK3β reduced HIF-1α protein and transcriptional activity and increased ubiquitination of HIF-1α in hypoxia, whereas pharmacologic inhibition of GSK3 or expression of siGSK3β promoted HIF-1α stabilization and activity. A mechanism through FBW7 was supported by the observed decrease in HIF-1α stabilization when FBW7 was overexpressed and both the elevation of HIF-1α levels and decrease in ubiquitinated HIF-1α when FBW7 was suppressed. Furthermore, HIF-1α associated with FBW7γ by co-immunoprecipitation, and the interaction was weakened by inhibition of GSK3 or mutation of GSK3β 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 GSK3β or FBW7. These data introduce a new mechanism for regulation of HIF-1α during hypoxia that utilizes phosphorylation to target HIF-1α for ubiquitin-dependent degradation through FBW7 and may identify new targets in the regulation of angiogenesis.

Bcl-2 family member Mcl-1 expression is reduced under hypoxia by the E3 ligase FBW7 contributing to BNIP3 induced cell death in glioma cells

“…FBW7 has been shown to be important in the degradation of Mcl-1 through the ubiquitination/proteosome pathway. 22 FBW7 has also been shown to be involved in the degradation of HIF-1 23 suggesting it plays a role in eliminating cell survival mechanisms under prolonged hypoxic conditions.…”

Understanding complexity in the HIF signaling pathway using systems biology and mathematical modeling

“…Besides the mTOR-mediated translational regulation, PKB/Akt has also been reported to be involved in the proteasomal degradation of HIF-1 [69]. This effect seems to involve the glycogen synthase kinase 3β (GSK3β) mediated phosphorylation of HIF-1 that facilitates its binding to the FBW7, an E3 ubiquitin ligase that recognizes GSK3β-phosphorylated proteins and targets them for proteasomal degradation [70].…”

FBW7 (F-box and WD Repeat Domain-Containing 7) Negatively Regulates Glucose Metabolism by Targeting the c-Myc/TXNIP (Thioredoxin-Binding Protein) Axis in Pancreatic Cancer

“…The transcription factors HIF1a and c-Myc increased the expression of glycolytic genes, thereby enhancing glycolysis and lactate production (16)(17)(18). HIF1a and c-Myc are well-characterized regulators of metabolism and are reported to be downstream substrates of FBW7 (19)(20)(21). This prompted us to investigate whether FBW7 is a negative regulator of cancer cell metabolism in pancreatic cancer.…”