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. Author manuscript; available in PMC: 2017 Dec 11.
Published in final edited form as: Gastroenterology. 2013 Jun;144(6):1194–1198. doi: 10.1053/j.gastro.2013.01.070

Table 1.

Strengths and Limitations of Various Models of Pancreatic Cancer and Pancreatitis

Pancreatic cancer models

Model Strengths Limitations
Subcutaneous xenograft model Ease of establishment
Ease of monitoring the tumor size
Recapitulation of human tumor histology (eg, desmoplasia) with use of human pancreatic cancer xenografts
Potential use of subcutaneous xenograft with pancreatic cancer tissue from patients in selecting therapy tailored to patient’s tumor
Unnatural milieu
Lack of modulation of tumor growth by immune system
Concerns regarding real representation of human disease by cell lines
Lack of metastasis and locoregional spread
Orthotopic model Tumor growth in natural milieu
Locoregional and metastatic spread with aggressive cell lines
Recapitulation of human tumor histology (eg, desmoplasia) with use of human pancreatic cancer xenografts
Technically challenging
Difficult to monitor tumor size requiring advanced techniques such as ultrasound
Lack of modulation of tumor growth by immune system
Genetically engineered model Recapitulation of genetic changes of pancreatic cancer
Use of immune-competent mice enables evaluation of effect of immune-surveillance on tumor growth
Concerns regarding relevance to human disease because the tumor’s genetic make-up is that of mouse
Cost of establishment of mouse colonies
Difficulty of monitoring tumor growth
Long delay in development of tumors

Models of pancreatitis

Cerulein model Convenient
Rapid induction
Reproducible
Similar histologic changes as human disease
Availability of corresponding in vitro model
Unknown clinical relevance
Less severity
Choline-deficient ethionine supplementation diet model Convenient
Noninvasive
Unknown clinical relevance
Contribution of hepatic and central nervous system changes to mortality, which is unchanged with pancreas-targeted therapies
Lack of corresponding in vitro model
Arginine model Convenient
Rapid induction
Unknown clinical relevance
Lack of corresponding in vitro model
Duct obstruction model Rapid induction
Clinically relevant
Invasive
Mild severity
Duct infusion model Rapid induction
Clinically relevant
Recapitulation of human disease in terms of severity and systemic changes
Infusion of different component of bile can help dissect their role in acute pancreatitis
Invasive
Difficult to establish the model