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Generation of Subcutaneous and Intrahepatic Human Hepatocellular Carcinoma Xenografts in Immunodeficient Mice
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Research Techniques Made Simple: Skin Carcinogenesis Models: Xenotransplantation Techniques
Maria Rosaria Mollo1, Dario Antonini2, Luisa Cirillo3
1CEINGE Biotecnologie Avanzate, Scarl, Napoli, Italy.
The Journal of Investigative Dermatology
|January 24, 2016
Summary
Xenotransplantation in immunodeficient mice is crucial for testing human squamous cell carcinoma (SCC) tumorigenic potential. Recent advances enhance in vivo models to study SCC cell behavior and tumor microenvironment interactions.
Area of Science:
- Oncology
- Immunology
- Cell Biology
Background:
- Xenotransplantation is a key method for evaluating human cell tumorigenicity in vivo.
- Immunodeficient mice are essential models for these studies, particularly for skin squamous cell carcinomas (SCCs).
- Understanding SCC behavior and its interaction with the tumor microenvironment is critical for developing effective therapies.
Purpose of the Study:
- To review basic technologies and recent advances in xenotransplantation for studying skin SCCs.
- To highlight various xenotransplantation techniques and their suitability for different experimental designs.
- To discuss methods for studying SCC cell interactions within a more physiologically relevant tumor environment.
Main Methods:
- Isolation and culture of SCC cells or direct injection into immunodeficient mice.
- Utilization of various immunodeficient mouse models tailored to specific tumorigenicity assays.
- Employing subcutaneous injections, epidermal-to-dermal junction injections, and grafting of organotypic cultures.
- Incorporating cancer-associated fibroblasts and real-time microscopy for studying cell interactions.
Main Results:
- Subcutaneous injection is a widely used, simple method but may not fully replicate the native tumor microenvironment.
- Alternative methods like epidermal-to-dermal injections and organotypic cultures offer more relevant tumor microenvironments.
- In vivo real-time tracking of SCC cell and fibroblast interactions is achievable with advanced techniques.
Conclusions:
- Xenotransplantation models are continuously evolving to better mimic the in vivo human SCC tumor microenvironment.
- Advances in xenotransplantation technologies facilitate the study of complex cell-cell interactions within SCCs.
- These refined models are vital for accurately assessing SCC tumorigenic potential and guiding therapeutic strategies.

