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Therapeutic Hypothesis Testing With Rodent Brain Tumor Models
Derek A Wainwright1,2,3, Craig M Horbinski1,4, Rintaro Hashizume1,5
1Department of Neurological Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Abstract:
The development and application of rodent models for preclinical testing of novel therapeutics and approaches for treating brain tumors has been a mainstay of neuro-oncology preclinical research for decades, and is likely to remain so into the foreseeable future. These models serve as an important point of entry for analyzing the potential efficacy of experimental therapies that are being considered for clinical trial evaluation. Although rodent brain tumor models have seen substantial change, particularly since the introduction of genetically engineered mouse models, certain principles associated with the use of these models for therapeutic testing are enduring, and form the basis for this review. Here we discuss the most common rodent brain tumor models while directing specific attention to their usefulness in preclinical evaluation of experimental therapies. These models include genetically engineered mice that spontaneously or inducibly develop brain tumors; syngeneic rodent models in which cultured tumor cells are engrafted into the same strain of rodent from which they were derived; and patient-derived xenograft models in which human tumor cells are engrafted in immunocompromised rodents. The emphasis of this review is directed to the latter.
Insights
Rodent models are crucial for preclinical testing of brain tumor therapeutics. This review emphasizes patient-derived xenografts for evaluating experimental therapies before clinical trials.
Area of Science:
- Neuro-oncology
- Preclinical Research
- Translational Medicine
Background:
- Rodent models have been foundational in neuro-oncology for decades.
- These models are essential for assessing experimental therapies prior to human trials.
- Advancements include genetically engineered mouse models, but core principles remain.
Purpose of the Study:
- To review common rodent brain tumor models.
- To evaluate their utility in preclinical therapeutic testing.
- To focus specifically on patient-derived xenograft models.
Main Methods:
- Discussion of genetically engineered mouse models.
- Overview of syngeneic rodent models.
- Detailed examination of patient-derived xenograft models.
Main Results:
- Genetically engineered models spontaneously or inducibly develop tumors.
- Syngeneic models involve engrafting tumor cells into syngeneic rodents.
- Patient-derived xenografts utilize human tumor cells in immunocompromised rodents.
Conclusions:
- Patient-derived xenografts are highlighted for their preclinical therapeutic evaluation potential.
- Rodent models continue to be vital for advancing brain tumor treatments.
- The review provides insights into selecting appropriate models for drug development.
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