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Updated: Jun 19, 2026

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An Orthotopic Murine Model of Human Prostate Cancer Metastasis
Published on: September 18, 2013
Serially heterotransplanted human prostate tumours as an experimental model
1Stanley S. Scott Cancer Center, Louisiana State University, Health Sciences Center, New Orleans, LA 70112, USA. lalb93@gmail.com
Journal of Cellular and Molecular Medicine
|October 31, 2009
Summary
Serial heterotransplantation of human prostate tumors in mice accurately models the original cancer. This preclinical model is superior for testing new prostate cancer therapies, including androgen-deprivation agents and anti-angiogenic drugs.
Area of Science:
- Oncology
- Preclinical Cancer Models
- Translational Research
Background:
- Accurate preclinical models are crucial for prostate cancer (PC) therapy development.
- Serial heterotransplantation of human PC tumors in immunodeficient mice is a key model.
- This model involves direct implantation and serial passage of patient tumor biopsies in vivo.
Purpose of the Study:
- To review over 30 years of data on human PC serial heterotransplantation.
- To evaluate the fidelity of heterotransplanted tumors compared to original patient tumors.
- To assess the utility of this model for preclinical cancer therapy research.
Main Methods:
- Characterization of heterotransplanted tumors: histopathology, cytology, karyotype, marker expression, hormone dependency, proliferation, and metastatic potential.
- Comparison of heterotransplanted tumors with original patient tumor specimens.
- Correlation of heterotransplant data with patient clinical outcomes where available.
Main Results:
- Serially heterotransplanted human tumors closely resemble their tumors of origin in various characteristics.
- The model demonstrates hormone dependency (androgen-dependent, partially, or independent) and metastatic potential.
- Stromal and vascular components are evaluated for similarity to the primary tumor.
Conclusions:
- Serial heterotransplantation provides a highly accurate preclinical model for prostate cancer.
- This model is more effective than older genetic or serially passaged models for evaluating novel PC therapies.
- The model is valuable for testing androgen-deprivation agents, anti-cancer drugs, anti-angiogenic compounds, and imaging agents.

