Statin prevents cancer development in chronic inflammation by blocking interleukin 33 expression

他汀类药物通过阻断白细胞介素 33 的表达来预防慢性炎症中的癌症发展

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作者:Jong Ho Park, Mahsa Mortaja, Heehwa G Son, Xutu Zhao, Lauren M Sloat, Marjan Azin, Jun Wang, Michael R Collier, Krishna S Tummala, Anna Mandinova, Nabeel Bardeesy, Yevgeniy R Semenov, Mari Mino-Kenudson, Shadmehr Demehri

Abstract

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.

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