Statin prevents cancer development in chronic inflammation by blocking interleukin 33 expression.
Jong Ho ParkMahsa MortajaHeehwa G SonXutu ZhaoLauren M SloatMarjan AzinJun WangMichael R CollierKrishna S TummalaAnna MandinovaNabeel El-BardeesyYevgeniy R SemenovMari A Mino-KenudsonShadhmer DemehriPublished in: Nature communications (2024)
Chronic inflammation is a major cause of cancer worldwide. Interleukin 33 (IL-33) is a critical initiator of cancer-prone chronic inflammation; however, its induction mechanism by environmental causes of chronic inflammation is unknown. Herein, we demonstrate that Toll-like receptor (TLR)3/4-TBK1-IRF3 pathway activation links environmental insults to IL-33 induction in the skin and pancreas inflammation. An FDA-approved drug library screen identifies pitavastatin to effectively suppress IL-33 expression by blocking TBK1 membrane recruitment/activation through the mevalonate pathway inhibition. Accordingly, pitavastatin prevents chronic pancreatitis and its cancer sequela in an IL-33-dependent manner. The IRF3-IL-33 axis is highly active in chronic pancreatitis and its associated pancreatic cancer in humans. Interestingly, pitavastatin use correlates with a significantly reduced risk of chronic pancreatitis and pancreatic cancer in patients. Our findings demonstrate that blocking the TBK1-IRF3-IL-33 signaling axis suppresses cancer-prone chronic inflammation. Statins present a safe and effective prophylactic strategy to prevent chronic inflammation and its cancer sequela.
Keyphrases
- papillary thyroid
- oxidative stress
- toll like receptor
- squamous cell
- immune response
- cardiovascular disease
- poor prognosis
- lymph node metastasis
- dendritic cells
- inflammatory response
- type diabetes
- coronary artery disease
- signaling pathway
- end stage renal disease
- emergency department
- gene expression
- long non coding rna
- drug induced
- young adults
- peritoneal dialysis
- newly diagnosed
- dna methylation
- nuclear factor
- human health
- climate change
- single cell