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Ductal obstruction promotes formation of preneoplastic lesions from the pancreatic ductal compartment
Author(s) -
Cheng Tao,
Zhang Zhiheng,
Jian Ziying,
Raulefs Susanne,
Schlitter Anna Melissa,
Steiger Katja,
Maeritz Nadja,
Zhao Yamin,
Shen Shanshan,
Zou Xiaoping,
Ceyhan Güralp O.,
Friess Helmut,
Kleeff Jörg,
Michalski Christoph W.,
Kong Bo
Publication year - 2018
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.31981
Subject(s) - kras , ductal cells , pancreatic cancer , pathology , ceruletide , ductal carcinoma , pancreatic duct , pancreatitis , carcinogenesis , cancer research , pancreas , biology , medicine , cancer , colorectal cancer , immunohistochemistry , breast cancer , cholecystokinin , receptor
Pancreatitis is a significant risk factor for pancreatic ductal adenocarcinoma (PDAC). Previous studies in mice have demonstrated that pancreatitis contributes to oncogenic Kras‐driven carcinogenesis, probably initiated in acinar cells; however, oncogenic Kras alone or in combination with caerulein‐induced pancreatitis is not sufficient in initiating PDAC from the ductal compartment. We thus introduced ductal obstruction – which induces a more severe form of pancreatitis – by pancreatic ductal ligation in mice harbouring oncogenic Kras. This induced a particular phenotype with highly proliferative nonmucinous cells with nuclear atypia. Around these lesions, there was a significant proliferation of activated fibroblasts and infiltration of immune cells, corroborating the pathological features of preneoplastic lesions. Lineage‐tracing experiments revealed that these preneoplastic cells derived from two distinctive cellular sources: acinar and ductal cells. Phenotypic characterisation revealed that the duct‐derived preneoplastic lesions show a high proliferative potential with persistent activation of tumour‐promoting inflammatory pathways while the acinar‐derived ones were less proliferative with persistent p53 activation. Furthermore, the duct‐derived preneoplastic cells have a particularly high nuclear‐to‐cytoplasmic ratio. These data demonstrate that ductal obstruction promotes preneoplastic lesion formation from the pancreatic ductal compartment.