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Pathology of genetically engineered mouse models of pancreatic exocrine cancer: Consensus report and recommendations

  • Ralph H. Hruban
  • , N. Volkan Adsay
  • , Jorge Albores-Saavedra
  • , Miriam R. Anver
  • , Andrew V. Biankin
  • , Gregory P. Boivin
  • , Emma E. Furth
  • , Toru Furukawa
  • , Alison Klein
  • , David S. Klimstra
  • , Gunter Kloppel
  • , Gregory Y. Lauwers
  • , Daniel S. Longnecker
  • , Jutta Luttges
  • , Anirban Maitra
  • , G. Johan A. Offerhaus
  • , Lucía Pérez-Gallego
  • , Mark Redston
  • , David A. Tuveson
  • Johns Hopkins Medical Institutions
  • Johns Hopkins Hospital
  • Wayne State University
  • Louisiana State University in Shreveport
  • SAIC-Frederick
  • University of Cincinnati College of Medicine
  • The University of Pennsylvania
  • Tokyo Women’s Medical University
  • Weill Cornell Medical College
  • Christian-Albrechts-University of Kiel
  • Massachusetts General Hospital
  • Dartmouth-Hitchcock Medical Center
  • Teaching Hospital University Homburg
  • Amsterdam University Medical Centers
  • Spanish National Cancer Research Centre (CNIO)
  • Brigham and Women's Hospital
  • University of Pennsylvania

Research output: Contribution to journalArticlepeer-review

347 Scopus citations

Abstract

Several diverse genetically engineered mouse models of pancreatic exocrine neoplasia have been developed. These mouse models have a spectrum of pathologic changes; however, until now, there has been no uniform nomenclature to characterize these changes. An international workshop, sponsored by The National Cancer Institute and the University of Pennsylvania, was held from December 1 to 3, 2004 with the goal of establishing an internationally accepted uniform nomenclature for the pathology of genetically engineered mouse models of pancreatic exocrine neoplasia. The pancreatic pathology in 12 existing mouse models of pancreatic neoplasia was reviewed at this workshop, and a standardized nomenclature with definitions and associated images was developed. It is our intention that this nomenclature will standardize the reporting of genetically engineered mouse models of pancreatic exocrine neoplasia, that it will facilitate comparisons between genetically engineered mouse models and human pancreatic disease, and that it will be broad enough to accommodate newly emerging mouse models of pancreatic neoplasia.

Original languageEnglish
Pages (from-to)95-106
Number of pages12
JournalCancer Research
Volume66
Issue number1
DOIs
StatePublished - 1 Jan 2006
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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