Glycolysis, via NADH-dependent dimerisation of CtBPs, regulates hypoxia-induced expression of CAIX and stem-like breast cancer cell survival.
Mira KreuzerArindam BanerjeeCharles N BirtsMatthew DarleyAli TavassoliMircea IvanJeremy P BlaydesPublished in: FEBS letters (2020)
Adaptive responses to hypoxia are mediated by the hypoxia-inducible factor (HIF) family of transcription factors. These responses include the upregulation of glycolysis to maintain ATP production. This also generates acidic metabolites, which require HIF-induced carbonic anhydrase IX (CAIX) for their neutralisation. C-terminal binding proteins (CtBPs) are coregulators of gene transcription and couple glycolysis with gene transcription due to their regulation by the glycolytic coenzyme NADH. Here, we find that experimental manipulation of glycolysis and CtBP function in breast cancer cells through multiple complementary approaches supports a hypothesis whereby the expression of known HIF-inducible genes, and CAIX in particular, adapts to available glucose in the microenvironment through a mechanism involving CtBPs. This novel pathway promotes the survival of stem cell-like cancer (SCLC) cells in hypoxia.
Keyphrases
- poor prognosis
- transcription factor
- genome wide identification
- endothelial cells
- stem cells
- genome wide
- high glucose
- breast cancer cells
- induced apoptosis
- copy number
- long non coding rna
- papillary thyroid
- cell proliferation
- type diabetes
- ms ms
- cell cycle arrest
- blood glucose
- signaling pathway
- diabetic rats
- dna methylation
- endoplasmic reticulum stress
- young adults
- blood pressure
- dna binding
- adipose tissue
- squamous cell
- free survival
- weight loss
- stress induced