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FBXW7 modulates cellular stress response and metastatic potential through ​HSF1 post-translational modification.

Nature cell biology | 2015

​Heat-shock factor 1 (​HSF1) orchestrates the heat-shock response in eukaryotes. Although this pathway has evolved to help cells adapt in the presence of challenging conditions, it is co-opted in cancer to support malignancy. However, the mechanisms that regulate ​HSF1 and thus cellular stress response are poorly understood. Here we show that the ubiquitin ligase ​FBXW7α interacts with ​HSF1 through a conserved motif phosphorylated by ​GSK3β and ​ERK1. ​FBXW7α ubiquitylates ​HSF1 and loss of ​FBXW7α results in impaired degradation of nuclear ​HSF1 and defective heat-shock response attenuation. ​FBXW7α is either mutated or transcriptionally downregulated in melanoma and ​HSF1 nuclear stabilization correlates with increased metastatic potential and disease progression. ​FBXW7α deficiency and subsequent ​HSF1 accumulation activates an invasion-supportive transcriptional program and enhances the metastatic potential of human melanoma cells. These findings identify a post-translational mechanism of regulation of the ​HSF1 transcriptional program both in the presence of exogenous stress and in cancer.

Pubmed ID: 25720964 RIS Download

Associated grants

  • Agency: NCI NIH HHS, United States
    Id: 1R01CA169784-02
  • Agency: NCI NIH HHS, United States
    Id: 1R01CA149655-04
  • Agency: NCI NIH HHS, United States
    Id: P30 CA016087
  • Agency: NCI NIH HHS, United States
    Id: R01 CA133379
  • Agency: NCI NIH HHS, United States
    Id: R01 CA202027
  • Agency: NCI NIH HHS, United States
    Id: R01 CA105129
  • Agency: NIGMS NIH HHS, United States
    Id: R21 GM110450
  • Agency: NIH HHS, United States
    Id: 1R24OD018339-01
  • Agency: NCI NIH HHS, United States
    Id: 1R01CA1638-01A1
  • Agency: NCI NIH HHS, United States
    Id: 1R01CA105129-08
  • Agency: NCI NIH HHS, United States
    Id: 1R01CA155234
  • Agency: NCI NIH HHS, United States
    Id: 1R01CA133379-06
  • Agency: NCI NIH HHS, United States
    Id: 5R01CA173636-03
  • Agency: Howard Hughes Medical Institute, United States

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