摘要：SummaryThe risk of pancreatic cancer is higher among people who are cigarette smokers than among non-smokers; however, the action mechanisms of cigarette metabolites are not yet fully understood. In this study, we investigated the effect of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) in cigarette smoking on chronic pancreatitis and pancreatic cancer as well as the biological mechanism of NNK causing malignant transformation. We show that smoking may promote Kras mutation and P16 promoter methylation from clinical samples and NNK markedly facilitates the growth and migration of pancreatic cancer cells via the activation of Sonic Hedgehog signaling. We demonstrate that NNK promotes acinar-to-ductal metastasis and pancreatic intraepithelial neoplasia in rats with chronic pancreatitis, accompanied by desmoplastic reaction and Gli1 overexpression. Together, we here present evidence that NNK provokes the progression of chronic pancreatitis toward pancreatic cancer and highlight potential strategies and targets for early prevention of pancreatic cancer and its therapeutics.Graphical abstractDisplay OmittedHighlights•Smoking is positively correlated withKrasmutation and P16 hypermethylation•NNK promotes acinar-to-ductal metastasis and preneoplasia lesions in rats•NNK promotes desmoplastic reaction and Gli1 expression in chronic pancreatitis•NNK facilitates the growth and migration of cancer via Sonic Hedgehog signalingHealth sciences; Cell biology; Cancer
