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A Protocol for Using Gene Set Enrichment Analysis to Identify the Appropriate Animal Model for Translational Research
Published on: August 16, 2017
Translational research challenges: finding the right animal models
1Nephrology Division, Texas Tech University Health Sciences Center, Lubbock, TX, USA. Sharma.prabhakar@ttuhsc.edu
Abstract:
Translation of scientific discoveries into meaningful human applications, particularly novel therapies of human diseases, requires development of suitable animal models. Experimental approaches to test new drugs in preclinical phases often necessitated animal models that not only replicate human disease in etiopathogenesis and pathobiology but also biomarkers development and toxicity prediction. Whereas the transgenic and knockout techniques have revolutionized manipulation of rodents and other species to get greater insights into human disease pathogenesis, we are far from generating ideal animal models of most human disease states. The challenges in using the currently available animal models for translational research, particularly for developing potentially new drugs for human disease, coupled with the difficulties in toxicity prediction have led some researchers to develop a scoring system for translatability. These aspects and the challenges in selecting an animal model among those that are available to study human disease pathobiology and drug development are the topics covered in this detailed review.
Insights
Developing ideal animal models for human diseases remains a significant challenge in translational research. This review discusses current limitations and strategies for improving animal models in drug development and toxicity prediction.
Area of Science:
- Biomedical Research
- Translational Science
- Drug Development
Background:
- Effective translation of scientific discoveries into human therapies relies heavily on suitable animal models.
- Current animal models often fail to fully replicate human disease etiopathogenesis, pathobiology, and toxicity prediction.
- Advancements in transgenic and knockout technologies offer insights but have not yet yielded ideal models for most human diseases.
Purpose of the Study:
- To review the challenges in developing and utilizing animal models for human disease research and drug development.
- To discuss the limitations of current animal models in predicting human toxicity and disease progression.
- To explore strategies for improving the translatability of animal models, including scoring systems.
Main Methods:
- Literature review of existing research on animal models in translational science.
- Analysis of challenges in disease replication, biomarker development, and toxicity prediction.
- Discussion of scoring systems for assessing animal model translatability.
Main Results:
- Significant gaps exist between current animal models and ideal human disease replication.
- Transgenic and knockout techniques have limitations in creating fully translatable models.
- Difficulties in toxicity prediction remain a major hurdle in preclinical drug development.
Conclusions:
- There is a critical need for improved animal models that better mimic human diseases for effective drug development.
- Existing models present challenges in pathobiology replication and toxicity prediction, impacting translational research.
- Developing standardized scoring systems is crucial for selecting and evaluating the translatability of animal models.
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