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Updated: May 6, 2026

Transplantation of Zebrafish Pediatric Brain Tumors into Immune-competent Hosts for Long-term Study of Tumor Cell Behavior and Drug Response
Published on: May 17, 2017
Precision animal models of tumors: Advances, challenges and clinical translation
Zhengyi Wang1,2, Xiaoying Wu3
1Department of Institute of Laboratory Animal Sciences, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Abstract:
Preclinical immunotherapy research relies heavily on animal tumor models, which can be broadly classified into four categories: genetically engineered, carcinogen-induced, spontaneous, and humanized transplantation platforms. While these systems mimic tumorigenesis, immune-microenvironment interactions, and therapeutic responses, their clinical translational utility is limited by species differences, incomplete immune reconstitution, and significant ethical concerns. This review synthesizes current approaches, systematically catalogs their respective strengths and limitations, and proposes integrated solutions that incorporate multi-omics datasets, artificial intelligence modeling, standardized protocols, and international consortia. Future research should prioritize the development of next-generation humanized platforms and virtual digital tumor models, and accelerate clinical translation through rigorous cross-species validation.
Insights
Preclinical immunotherapy research uses animal tumor models, but these have limitations. This review synthesizes current approaches and proposes integrated solutions for better clinical translation.
Area of Science:
- Immunotherapy
- Oncology
- Translational Research
Background:
- Preclinical immunotherapy research heavily utilizes animal tumor models.
- These models include genetically engineered, carcinogen-induced, spontaneous, and humanized transplantation platforms.
- Current models face limitations in clinical translational utility due to species differences, incomplete immune reconstitution, and ethical concerns.
Purpose of the Study:
- To synthesize current approaches in animal tumor models for preclinical immunotherapy.
- To systematically catalog the strengths and limitations of existing models.
- To propose integrated solutions for enhancing the clinical translational utility of these models.
Main Methods:
- Literature review and synthesis of current approaches in animal tumor models.
- Systematic cataloging of model strengths and limitations.
- Proposal of integrated solutions including multi-omics, AI, standardized protocols, and consortia.
Main Results:
- Identified four main categories of animal tumor models.
- Highlighted limitations of current models, including species differences and ethical concerns.
- Proposed integrated solutions for improved preclinical research and clinical translation.
Conclusions:
- Future research should focus on next-generation humanized platforms and virtual digital tumor models.
- Accelerating clinical translation requires rigorous cross-species validation.
- Integrated solutions incorporating multi-omics, AI, and international collaboration are crucial for advancing immunotherapy research.
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