Obesity-associated NLRC4 inflammasome activation drives breast cancer progression.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 27708283.
- Also identified by DOI 10.1038/ncomms13007 and PMC identifier 5059727.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Obesity is associated with an increased risk of developing breast cancer and is also associated with worse clinical prognosis. The mechanistic link between obesity and breast cancer progression remains unclear, and there has been no development of specific treatments to improve the outcome of obese cancer patients. Here we show that obesity-associated NLRC4 inflammasome activation/ interleukin (IL)-1 signalling promotes breast cancer progression. The tumour microenvironment in the context of obesity induces an increase in tumour-infiltrating myeloid cells with an activated NLRC4 inflammasome that in turn activates IL-1β, which drives disease progression through adipocyte-mediated vascular endothelial growth factor A (VEGFA) expression and angiogenesis. Further studies show that treatment of mice with metformin inhibits obesity-associated tumour progression associated with a marked decrease in angiogenesis. This report provides a causal mechanism by which obesity promotes breast cancer progression and lays out a foundation to block NLRC4 inflammasome activation or IL-1β signalling transduction that may be useful for the treatment of obese cancer patients.
Medical subject headings
- Breast Neoplasms
- CARD Signaling Adaptor Proteins
- Calcium-Binding Proteins
- Inflammasomes
- Interleukin-1beta
- Obesity
- Vascular Endothelial Growth Factor A