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. 2021 Oct 8;13(10):1638. doi: 10.3390/pharmaceutics13101638

Table 1.

Various models of pancreatic cancer for preclinical studies.

In Vitro In Vivo
Models Cell Line Patient-Derived
Organoid
Cell Line Xenograft Patient-Derived Xenograft Genetically Modified Mouse Model (GEMM)
TME - +++ + ++ ++
Immune system - ++ + + +++
Pros
  • Fast and easy growth

  • Rapid drug screening

  • Mimic complex TME and stroma

  • Orthotopically transplantable

  • Useful for testing drug efficacy and safety

  • Mirror patient response to drug

  • Personalized drug regimen

  • Useful tool for oncogenic mutation investigation and biomarker discovery

Cons
  • Genetically uniform

  • New model and needs further analysis

  • Limited TME and immune system

  • Engraftment difficulties

  • Long duration of growth

  • Selection for aggressive tumors

  • Species discrepancy

  • High cost and complexity of GEMM generation

Parameters are appreciated as abundant (+++), moderate (++), minimal (+) and none (-).