| Literature DB >> 27720937 |
Adam P Deveau1, Victoria L Bentley2, Jason N Berman3.
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 allows for the identification of relevant therapies while simultaneously evaluating drug toxicity, thus circumventing the limitations of target-centric approaches.Entities:
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Year: 2016 PMID: 27720937 DOI: 10.1016/j.exphem.2016.09.012
Source DB: PubMed Journal: Exp Hematol ISSN: 0301-472X Impact factor: 3.084