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Updated: Aug 22, 2025

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A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
13.2K
In Vivo Models for Prostate Cancer Research
Robert Adamiecki1,2, Anita Hryniewicz-Jankowska2,3, Maria A Ortiz2,4
1Rutgers New Jersey Medical School, Rutgers University, Newark, NJ 07103, USA.
Cancers
|November 11, 2022
Summary
This review compares various in vivo models for studying prostate cancer (PCa), highlighting their genetic alterations, signaling pathways, and tumor progression stages. These models aid in translating mouse prostate cancer research to human applications.
Area of Science:
- Oncology
- Genetics
- Animal Models
Background:
- Prostate cancer (PCa) is the most common cancer diagnosis in US men.
- Understanding PCa progression requires effective preclinical models.
- Mouse models are crucial due to genomic similarities with humans.
Purpose of the Study:
- To compare and contrast various in vivo models of prostate cancer.
- To analyze genetic alterations, signaling pathways, and tumor progression in PCa models.
- To evaluate the utility of different models for translating findings to human PCa.
Main Methods:
- Review of genetically engineered mouse models (conditional/constitutive knockouts).
- Inclusion of 2D cell lines, 3D organoids/spheroids, xenografts, allografts, and patient-derived models.
- Analysis of model applications, advantages, disadvantages, cost, and ease of use.
Main Results:
- Different models offer unique applications, benefits, and drawbacks.
- All models facilitate the translation of mouse prostate tumor progression to human relevance.
- The inability of native mouse prostates to spontaneously form carcinoma is a key consideration.
Conclusions:
- Various in vivo models significantly advance our understanding of prostate cancer.
- Genomic similarities between mice and humans enhance the translational value of PCa models.
- Continued research using these models will expand knowledge of PCa.

