Related Experiment Video
Updated: Jul 30, 2025

08:43
Orthotopic Mouse Model of Colorectal Cancer
Published on: December 4, 2007
45.7K
Experimental Murine Models for Colorectal Cancer Research
Íris Neto1, João Rocha1, Maria Manuela Gaspar1
1Research Institute for Medicines (iMed.ULisboa), Faculdade de Farmácia, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal.
Cancers
|May 13, 2023
Summary
This review examines various animal models for colorectal cancer (CRC), including carcinogen-induced models (CIMs) and genetically engineered mouse models (GEMMs). Patient-derived xenografts (PDX) offer the most reliable preclinical drug development due to their preserved pathological and molecular traits.
Area of Science:
- Oncology
- Translational Research
- Preclinical Models
Background:
- Colorectal cancer (CRC) is a leading global malignancy, necessitating robust research models.
- Existing murine models include carcinogen-induced models (CIMs) and genetically engineered mouse models (GEMMs).
- CIMs are useful for studying inflammation-driven carcinogenesis and chemoprevention strategies.
Purpose of the Study:
- To review and compare diverse murine models for colorectal cancer (CRC) research.
- To evaluate the clinical relevance, advantages, and limitations of each model type.
- To highlight the utility of models in understanding CRC biology and developing therapies.
Main Methods:
- Review of established carcinogen-induced models (CIMs) for CRC.
- Analysis of genetically engineered mouse models (GEMMs) for CRC.
- Evaluation of patient-derived xenografts (PDX) for preclinical drug development.
Main Results:
- GEMMs are valuable for studying the tumor microenvironment and immune responses in CRC.
- Orthotopic injection models have limitations due to restricted genetic diversity of cell lines.
- Patient-derived xenografts (PDX) best retain the pathological and molecular characteristics of human CRC.
Conclusions:
- Murine CRC models are crucial for advancing CRC understanding and treatment.
- Patient-derived xenografts (PDX) are highly reliable for preclinical drug development.
- Further research is needed to develop models that fully recapitulate CRC pathophysiology.

