A critical review of animal models used in acute myeloid leukemia pathophysiology

dc.contributor.authorSkayneh, Hala
dc.contributor.authorJishi, Batoul
dc.contributor.authorHleihel, Rita S.
dc.contributor.authorHamieh, Maguy
dc.contributor.authorDarwiche, Nadine D.
dc.contributor.authorBazarbachi, Ali Abdul Hamid
dc.contributor.authorEl-Sabban, Marwan E.
dc.contributor.authorEl-Hajj, Hiba Ahmad
dc.contributor.departmentExperimental Pathology, Microbiology, and Immunology
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.departmentInternal Medicine
dc.contributor.departmentBiochemistry and Molecular Genetics
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:39:01Z
dc.date.available2025-01-24T11:39:01Z
dc.date.issued2019
dc.description.abstractAcute myeloid leukemia (AML) is one of the most frequent, complex, and heterogeneous hematological malignancies. AML prognosis largely depends on acquired cytogenetic, epigenetic, and molecular abnormalities. Despite the improvement in understanding the biology of AML, survival rates remain quite low. Animal models offer a valuable tool to recapitulate different AML subtypes, and to assess the potential role of novel and known mutations in disease progression. This review provides a comprehensive and critical overview of select available AML animal models. These include the non-mammalian Zebrafish and Drosophila models as well as the mammalian rodent systems, comprising rats and mice. The suitability of each animal model, its contribution to the advancement of knowledge in AML pathophysiology and treatment, as well as its advantages and limitations are discussed. Despite some limitations, animal models represent a powerful approach to assess toxicity, and permit the design of new therapeutic strategies. © 2019 by the authors.
dc.identifier.doihttps://doi.org/10.3390/genes10080614
dc.identifier.eid2-s2.0-85071687857
dc.identifier.pmid31412687
dc.identifier.urihttp://hdl.handle.net/10938/29151
dc.language.isoen
dc.publisherMDPI AG
dc.relation.ispartofGenes
dc.sourceScopus
dc.subjectDrosophila
dc.subjectEto-1
dc.subjectFlt3 itd
dc.subjectIdh1/2
dc.subjectMice
dc.subjectNpm-1
dc.subjectRats
dc.subjectZebrafish
dc.subjectAnimals
dc.subjectCarcinogens
dc.subjectDisease models, animal
dc.subjectDrosophila melanogaster
dc.subjectLeukemia, myeloid, acute
dc.subjectMutagenesis
dc.subjectOncogenic viruses
dc.subjectCarcinogen
dc.subjectAcute myeloid leukemia
dc.subjectAnimal model
dc.subjectMouse model
dc.subjectNod scid gamma mouse
dc.subjectNonhuman
dc.subjectPathophysiology
dc.subjectRat model
dc.subjectReview
dc.subjectScid mouse
dc.subjectTransgenic mouse
dc.subjectZebra fish
dc.subjectAnimal
dc.subjectDisease model
dc.subjectMouse
dc.subjectPathogenicity
dc.subjectPathology
dc.subjectRat
dc.subjectTumor virus
dc.titleA critical review of animal models used in acute myeloid leukemia pathophysiology
dc.typeReview

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