Cancer Cell
Volume 22, Issue 6, 11 December 2012, Pages 737-750
Journal home page for Cancer Cell

Article
Identification of Sox9-Dependent Acinar-to-Ductal Reprogramming as the Principal Mechanism for Initiation of Pancreatic Ductal Adenocarcinoma

https://doi.org/10.1016/j.ccr.2012.10.025Get rights and content
Under an Elsevier user license
open archive

Summary

Tumors are largely classified by histologic appearance, yet morphologic features do not necessarily predict cellular origin. To determine the origin of pancreatic ductal adenocarcinoma (PDA), we labeled and traced pancreatic cell populations after induction of a PDA-initiating Kras mutation. Our studies reveal that ductal and stem-like centroacinar cells are surprisingly refractory to oncogenic transformation, whereas acinar cells readily form PDA precursor lesions with ductal features. We show that formation of acinar-derived premalignant lesions depends on ectopic induction of the ductal gene Sox9. Moreover, when concomitantly expressed with oncogenic Kras, Sox9 accelerates formation of premalignant lesions. These results provide insight into the cellular origin of PDA and suggest that its precursors arise via induction of a duct-like state in acinar cells.

Highlights

► Preneoplastic lesions rarely arise from pancreatic ductal/centroacinar cells ► Acinar cells are the predominant cells of origin for pancreatic preneoplastic lesions ► Initiation of pancreatic cancer depends on acinar induction of the ductal gene Sox9 ► Sox9 synergizes with KrasG12D and injury in acinar-to-ductal cell reprogramming

Cited by (0)

6

These authors contributed equally to this work