PUBLICATION
            Using zebrafish models of leukemia to streamline drug screening and discovery
- Authors
 - Deveau, A.P., Bentley, V.L., Berman, J.N.
 - ID
 - ZDB-PUB-161011-7
 - Date
 - 2017
 - Source
 - Experimental hematology 45: 1-9 (Review)
 - Registered Authors
 - Bentley, Victoria, Berman, Jason, Deveau, Adam
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Disease Models, Animal
 - Drug Evaluation, Preclinical*
 - Animals
 - Humans
 - Antineoplastic Agents/pharmacology*
 - Antineoplastic Agents/therapeutic use
 - Drug Discovery*
 - Leukemia/drug therapy
 - Xenograft Model Antitumor Assays
 - Zebrafish*
 - High-Throughput Screening Assays*
 - Animals, Genetically Modified
 - Genomics/methods
 - Phenotype
 
 - PubMed
 - 27720937 Full text @ Exp. Hematol.
 
            Citation
        
        
            Deveau, A.P., Bentley, V.L., Berman, J.N. (2017) Using zebrafish models of leukemia to streamline drug screening and discovery. Experimental hematology. 45:1-9.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Current treatment strategies for acute leukemias largely rely on nonspecific cytotoxic drugs that result in high therapy-related morbidity and mortality. Cost effective, pertinent animal models are needed to link in vitro studies with the development of new therapeutic agents in clinical trials on a high-throughput scale. However, targeted therapies have had limited success moving from bench-to-clinic, often due to unexpected off-target effects. The zebrafish has emerged as a reliable in vivo tool for modeling human leukemia. Zebrafish genetic and xenograft models of acute leukemia provide an unprecedented opportunity to conduct rapid phenotype-based screens. This prospect allows for the identification of relevant therapies, while simultaneously evaluating drug toxicity, circumventing the limitations of target-centric approaches.
            
    
        
        
    
    
    
                
                    
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                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping