Obesity-associated NLRC4 inflammasome activation drives breast cancer progression.
Ryan KolbLiem PhanNicholas BorcherdingYinghong LiuFang YuanAnn M JanowskiQing XieKathleen R MarkanWei LiMatthew J PotthoffEnrique Fuentes-MatteiLesley G ElliesC Michael KnudsonMong-Hong LeeSai-Ching J YeungSuzanne L CasselFayyaz S SutterwalaWeizhou ZhangPublished in: Nature communications (2016)
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.
Keyphrases
- weight loss
- insulin resistance
- metabolic syndrome
- high fat diet induced
- type diabetes
- vascular endothelial growth factor
- weight gain
- adipose tissue
- bariatric surgery
- skeletal muscle
- signaling pathway
- bone marrow
- cell death
- body mass index
- young adults
- dendritic cells
- smoking cessation
- endoplasmic reticulum stress
- case control