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- W3017039682 abstract "Cancer is the second leading cause of death in the world. Given that cancer is a highly individualized disease, predicting the best chemotherapeutic treatment for individual patients can be difficult. Ex vivo models such as mouse patient-derived xenografts (PDX) and organoids are being developed to predict patient-specific chemosensitivity profiles before treatment in the clinic. Although promising, these models have significant disadvantages including long growth times that introduce genetic and epigenetic changes to the tumor. The zebrafish xenograft assay is ideal for personalized medicine. Imaging of the small, transparent fry is unparalleled among vertebrate organisms. In addition, the speed (5-7 days) and small patient tissue requirements (100-200 cells per animal) are unique features of the zebrafish xenograft model that enable patient-specific chemosensitivity analyses." @default.
- W3017039682 created "2020-04-24" @default.
- W3017039682 creator A5001183315 @default.
- W3017039682 creator A5073768342 @default.
- W3017039682 creator A5076186971 @default.
- W3017039682 date "2020-07-01" @default.
- W3017039682 modified "2023-10-16" @default.
- W3017039682 title "Zebrafish Xenografts for Drug Discovery and Personalized Medicine" @default.
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- W3017039682 doi "https://doi.org/10.1016/j.trecan.2020.03.012" @default.
- W3017039682 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32312681" @default.
- W3017039682 hasPublicationYear "2020" @default.
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