The cell cycle regulator 14-3-3σ opposes and reverses cancer metabolic reprogramming.
basic_science · Level V
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- Record sourced from PubMed, PMID 26179207.
- Also identified by DOI 10.1038/ncomms8530 and PMC identifier 4507299.
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Abstract
Extensive reprogramming of cellular energy metabolism is a hallmark of cancer. Despite its importance, the molecular mechanism controlling this tumour metabolic shift remains not fully understood. Here we show that 14-3-3σ regulates cancer metabolic reprogramming and protects cells from tumorigenic transformation. 14-3-3σ opposes tumour-promoting metabolic programmes by enhancing c-Myc poly-ubiquitination and subsequent degradation. 14-3-3σ demonstrates the suppressive impact on cancer glycolysis, glutaminolysis, mitochondrial biogenesis and other major metabolic processes of tumours. Importantly, 14-3-3σ expression levels predict overall and recurrence-free survival rates, tumour glucose uptake and metabolic gene expression in breast cancer patients. Thus, these results highlight that 14-3-3σ is an important regulator of tumour metabolism, and loss of 14-3-3σ expression is critical for cancer metabolic reprogramming. We anticipate that pharmacologically elevating the function of 14-3-3σ in tumours could be a promising direction for targeted anticancer metabolism therapy development in future.
Medical subject headings
- 14-3-3 Proteins
- Biomarkers, Tumor
- Breast Neoplasms
- Energy Metabolism
- Exoribonucleases
- Gene Expression Regulation, Neoplastic
- Proto-Oncogene Proteins c-myc