Atypical flat lesions derive from pancreatic acinar cells

Guido von Figura, Leonie Fahrenkrog-Petersen, Ana Hidalgo-Sastre, Daniel Hartmann, Norbert Hüser, Roland M. Schmid, Matthias Hebrok, Nilotpal Roy, Irene Esposito

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Objectives Pancreatic ductal adenocarcinoma (PDAC) is thought to derive from different precursor lesions including the recently identified atypical flat lesions (AFL). While all precursor lesions and PDAC share ductal characteristics, there is an ongoing debate about the cellular origin of the different PDAC precursor lesions. In particular, pancreatic acinar cells have previously been shown to display a remarkable plasticity being able to undergo ductal dedifferentiation in the context of oncogenic stimuli. Methods Histological analyses were performed in a murine PDAC model that specifically expresses oncogenic Kras in adult pancreatic acinar cells. Occurrence, characterization, and lineage tracing of AFLs were investigated. Results Upon expression of oncogenic Kras in adult pancreatic acinar cells, AFLs with typical morphology and expression profile arise. Lineage tracing confirmed that the AFLs were of acinar origin. Conclusions Using a murine PDAC model, this study identifies pancreatic acinar cells as a cellular source for AFLs.

Original languageEnglish
Pages (from-to)350-353
Number of pages4
JournalPancreatology
Volume17
Issue number3
DOIs
StatePublished - May 2017
Externally publishedYes

Keywords

  • AFL
  • IPMN
  • PanIN
  • Pancreatic cancer

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