Animal Models: Challenges and Opportunities to Determine Optimal Experimental Models of Pancreatitis and Pancreatic Cancer
- PMID: 31206467
- PMCID: PMC6581211
- DOI: 10.1097/MPA.0000000000001335
Animal Models: Challenges and Opportunities to Determine Optimal Experimental Models of Pancreatitis and Pancreatic Cancer
Abstract
At the 2018 PancreasFest meeting, experts participating in basic research met to discuss the plethora of available animal models for studying exocrine pancreatic disease. In particular, the discussion focused on the challenges currently facing the field and potential solutions. That meeting culminated in this review, which describes the advantages and limitations of both common and infrequently used models of exocrine pancreatic disease, namely, pancreatitis and exocrine pancreatic cancer. The objective is to provide a comprehensive description of the available models but also to provide investigators with guidance in the application of these models to investigate both environmental and genetic contributions to exocrine pancreatic disease. The content covers both nongenic and genetically engineered models across multiple species (large and small). Recommendations for choosing the appropriate model as well as how to conduct and present results are provided.
Conflict of interest statement
Disclosure
A.U. is a member of the American Board of Pediatrics, Subboard of Pediatric Gastroenterology; Associate Editor of
Figures
Similar articles
-
Pathology of genetically engineered mouse models of pancreatic exocrine cancer: consensus report and recommendations.Cancer Res. 2006 Jan 1;66(1):95-106. doi: 10.1158/0008-5472.CAN-05-2168. Cancer Res. 2006. PMID: 16397221
-
Bmi1 is required for regeneration of the exocrine pancreas in mice.Gastroenterology. 2012 Sep;143(3):821-831.e2. doi: 10.1053/j.gastro.2012.05.009. Epub 2012 May 17. Gastroenterology. 2012. PMID: 22609312 Free PMC article.
-
Mice lacking the transcription factor Mist1 exhibit an altered stress response and increased sensitivity to caerulein-induced pancreatitis.Am J Physiol Gastrointest Liver Physiol. 2007 Apr;292(4):G1123-32. doi: 10.1152/ajpgi.00512.2006. Epub 2006 Dec 14. Am J Physiol Gastrointest Liver Physiol. 2007. PMID: 17170023
-
Evaluation of two novel peptide safety markers for exocrine pancreatic toxicity.Toxicol Sci. 2007 Mar;96(1):184-93. doi: 10.1093/toxsci/kfl190. Epub 2006 Dec 14. Toxicol Sci. 2007. PMID: 17169977
-
Disorders of the Pancreas.Prim Care. 2023 Sep;50(3):391-409. doi: 10.1016/j.pop.2023.03.005. Epub 2023 May 24. Prim Care. 2023. PMID: 37516510 Review.
Cited by
-
Acute pancreatitis-induced islet dysfunction in ferrets.Pancreatology. 2021 Aug;21(5):839-847. doi: 10.1016/j.pan.2021.04.008. Epub 2021 May 11. Pancreatology. 2021. PMID: 33994067 Free PMC article.
-
Targeted animal models for preclinical assessment of cellular and gene therapies in pancreatic and liver diseases: regulatory and practical insights.Cytotherapy. 2025 Mar;27(3):259-278. doi: 10.1016/j.jcyt.2024.11.008. Epub 2024 Nov 19. Cytotherapy. 2025. PMID: 39755978 Review.
-
Molecular mechanisms of pain in acute pancreatitis: recent basic research advances and therapeutic implications.Front Mol Neurosci. 2023 Dec 22;16:1331438. doi: 10.3389/fnmol.2023.1331438. eCollection 2023. Front Mol Neurosci. 2023. PMID: 38188196 Free PMC article. Review.
-
Functional role of IL-19 in a mouse model of L-arginine-induced pancreatitis and related lung injury.Exp Anim. 2024 May 3;73(2):175-185. doi: 10.1538/expanim.23-0094. Epub 2023 Dec 6. Exp Anim. 2024. PMID: 38057085 Free PMC article.
-
Serum biomarkers for chronic pancreatitis pain patterns.Pancreatology. 2021 Dec;21(8):1411-1418. doi: 10.1016/j.pan.2021.09.016. Epub 2021 Sep 30. Pancreatology. 2021. PMID: 34602367 Free PMC article.
References
-
- Lampel M, Kern HF. Acute interstitial pancreatitis in the rat induced by excessive doses of a pancreatic secretagogue. Virchows Arch A Pathol Anat Histol. 1977;373:97–117. - PubMed
-
- Watanabe O, Baccino FM, Steer ML, et al. Supramaximal caerulein stimulation and ultrastructure of rat pancreatic acinar cell: early morphological changes during development of experimental pancreatitis. Am J Physiol. 1984;246:G457–G467. - PubMed
-
- Nathan JD, Patel AA, McVey DC, et al. Capsaicin vanilloid receptor-1 mediates substance P release in experimental pancreatitis. Am J Physiol Gastrointest Liver Physiol. 2001;281:G1322–1328. - PubMed
-
- Kaiser AM, Saluja AK, Sengupta A, et al. Relationship between severity, necrosis, and apoptosis in five models of experimental acute pancreatitis. Am J Physiol. 1995;269:C1295–1304. - PubMed
-
- Klauss S, Schorn S, Teller S, et al. Genetically induced vs. classical animal models of chronic pancreatitis: a critical comparison. FASEB J. 2018;32:5778–5792. - PubMed
Publication types
MeSH terms
Grants and funding
- R13 DK118902/DK/NIDDK NIH HHS/United States
- R01 DK118752/DK/NIDDK NIH HHS/United States
- I01 BX004306/BX/BLRD VA/United States
- K01 DK120737/DK/NIDDK NIH HHS/United States
- K08 AA025112/AA/NIAAA NIH HHS/United States
- R01 CA177857/CA/NCI NIH HHS/United States
- T32 NS007433/NS/NINDS NIH HHS/United States
- P01 DK098108/DK/NIDDK NIH HHS/United States
- P30 CA086862/CA/NCI NIH HHS/United States
- K01 AA019996/AA/NIAAA NIH HHS/United States
- P01 CA163200/CA/NCI NIH HHS/United States
- I01 BX003250/BX/BLRD VA/United States
- T32 NS086749/NS/NINDS NIH HHS/United States
- R01 NS050758/NS/NINDS NIH HHS/United States
- U01 DK108306/DK/NIDDK NIH HHS/United States
- R01 NS031826/NS/NINDS NIH HHS/United States
- P30 DK054759/DK/NIDDK NIH HHS/United States
- U01 DK108314/DK/NIDDK NIH HHS/United States
- P50 AA011999/AA/NIAAA NIH HHS/United States
- R01 CA223204/CA/NCI NIH HHS/United States
- R01 DK054021/DK/NIDDK NIH HHS/United States
- U01 DK108334/DK/NIDDK NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous