Study human pancreatic cancer in mice: How close are they?

Yuqing Zhang, Leon Chen, Jingxuan Yang, Jason B. Fleming, Paul J. Chiao, Craig D. Logsdon, Min Li

Research output: Contribution to journalReview articlepeer-review

14 Scopus citations

Abstract

Pancreatic cancer is the fourth leading cause of cancer deaths and is characterized by dismal prognosis. Xenograft and genetically engineered mouse (GEM) models have recapitulated critical elements of human pancreatic cancer, providing useful tools to probe the underlying cause of cancer etiology. In this review, we provide a brief description of the common genetic lesions that occur during the development of pancreatic cancer. Next, we describe the strengths and weaknesses of these two models and highlight key discoveries each has made. Although the relative merits of GEM and xenograft pancreatic cancer mouse models are subject to debate, both systems have and will continue to yield essential insights in understanding pancreatic cancer etiology. This information is critical for the development of new methods to screen, treat, and prevent pancreatic cancer.

Original languageEnglish (US)
Pages (from-to)110-118
Number of pages9
JournalBiochimica et Biophysica Acta - Reviews on Cancer
Volume1835
Issue number1
DOIs
StatePublished - Jan 2013
Externally publishedYes

Keywords

  • Animal model
  • Gene function
  • Pancreatic cancer
  • Tumor microenvironment

ASJC Scopus subject areas

  • Oncology
  • Genetics
  • Cancer Research

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