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XBP1 promotes triple-negative breast cancer by controlling the HIF1α pathway.

Nature | 2014

Cancer cells induce a set of adaptive response pathways to survive in the face of stressors due to inadequate vascularization. One such adaptive pathway is the unfolded protein (UPR) or endoplasmic reticulum (ER) stress response mediated in part by the ER-localized transmembrane sensor IRE1 (ref. 2) and its substrate XBP1 (ref. 3). Previous studies report UPR activation in various human tumours, but the role of XBP1 in cancer progression in mammary epithelial cells is largely unknown. Triple-negative breast cancer (TNBC)--a form of breast cancer in which tumour cells do not express the genes for oestrogen receptor, progesterone receptor and HER2 (also called ERBB2 or NEU)--is a highly aggressive malignancy with limited treatment options. Here we report that XBP1 is activated in TNBC and has a pivotal role in the tumorigenicity and progression of this human breast cancer subtype. In breast cancer cell line models, depletion of XBP1 inhibited tumour growth and tumour relapse and reduced the CD44(high)CD24(low) population. Hypoxia-inducing factor 1α (HIF1α) is known to be hyperactivated in TNBCs. Genome-wide mapping of the XBP1 transcriptional regulatory network revealed that XBP1 drives TNBC tumorigenicity by assembling a transcriptional complex with HIF1α that regulates the expression of HIF1α targets via the recruitment of RNA polymerase II. Analysis of independent cohorts of patients with TNBC revealed a specific XBP1 gene expression signature that was highly correlated with HIF1α and hypoxia-driven signatures and that strongly associated with poor prognosis. Our findings reveal a key function for the XBP1 branch of the UPR in TNBC and indicate that targeting this pathway may offer alternative treatment strategies for this aggressive subtype of breast cancer.

Pubmed ID: 24670641 RIS Download

Associated grants

  • Agency: NCI NIH HHS, United States
    Id: K99 CA175290
  • Agency: NIAID NIH HHS, United States
    Id: AI32412
  • Agency: NCI NIH HHS, United States
    Id: R01 CA112663
  • Agency: NCI NIH HHS, United States
    Id: P30 CA016086
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM007753
  • Agency: NCI NIH HHS, United States
    Id: P50 CA058223
  • Agency: NCI NIH HHS, United States
    Id: R00 CA160351
  • Agency: NHGRI NIH HHS, United States
    Id: R01HG004069
  • Agency: NHGRI NIH HHS, United States
    Id: R01 HG004069
  • Agency: NCI NIH HHS, United States
    Id: CA112663
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI032412
  • Agency: NCI NIH HHS, United States
    Id: K99CA175290

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