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Updated: Feb 11, 2026

Establishment of a Human Multiple Myeloma Xenograft Model in the Chicken to Study Tumor Growth, Invasion and Angiogenesis
Published on: May 1, 2015
Mouse models of multiple myeloma: technologic platforms and perspectives.
Marco Rossi1, Cirino Botta1, Mariamena Arbitrio1
1Department of Experimental and Clinical Medicine, "Magna Graecia" University of Catanzaro, Catanzaro, Italy.
Pre-clinical models are crucial for multiple myeloma (MM) research. This review details various murine, transgenic, and humanized MM models, highlighting their strengths and weaknesses for therapeutic development.
Area of Science:
- Oncology
- Hematology
- Pre-clinical Research
Background:
- Murine models are essential for studying multiple myeloma (MM) biology and testing new therapies.
- Recent advancements have led to diverse pre-clinical models that mimic MM's complexity.
- Choosing the appropriate model is critical for research success.
Purpose of the Study:
- To review current pre-clinical murine, transgenic, and humanized models for multiple myeloma.
- To analyze the advantages and disadvantages of each model type.
- To guide researchers in selecting the most suitable model for their specific research objectives.
Main Methods:
- Review of published literature on pre-clinical multiple myeloma models.
- Categorization of models including spontaneous, transgenic, xenograft, and humanized systems.
- Comparative analysis of model systems based on biological fidelity and research applicability.
Main Results:
- Various models exist, including spontaneous/transgenic murine MM, xenografts of human MM cell lines, and humanized models engrafting primary MM cells.
- Each model type offers unique advantages for studying specific aspects of MM.
- Key limitations and strengths are identified for each model, influencing their suitability for different research aims.
Conclusions:
- A range of sophisticated pre-clinical models are available for multiple myeloma research.
- Understanding the specific advantages and limitations of each model is vital for effective therapeutic development and disease research.
- This review provides a framework for selecting optimal models to advance multiple myeloma studies.
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