A critical review of animal models used in acute myeloid leukemia pathophysiology
| dc.contributor.author | Skayneh, Hala | |
| dc.contributor.author | Jishi, Batoul | |
| dc.contributor.author | Hleihel, Rita S. | |
| dc.contributor.author | Hamieh, Maguy | |
| dc.contributor.author | Darwiche, Nadine D. | |
| dc.contributor.author | Bazarbachi, Ali Abdul Hamid | |
| dc.contributor.author | El-Sabban, Marwan E. | |
| dc.contributor.author | El-Hajj, Hiba Ahmad | |
| dc.contributor.department | Experimental Pathology, Microbiology, and Immunology | |
| dc.contributor.department | Anatomy, Cell Biology, and Physiological Sciences | |
| dc.contributor.department | Internal Medicine | |
| dc.contributor.department | Biochemistry and Molecular Genetics | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T11:39:01Z | |
| dc.date.available | 2025-01-24T11:39:01Z | |
| dc.date.issued | 2019 | |
| dc.description.abstract | Acute 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.doi | https://doi.org/10.3390/genes10080614 | |
| dc.identifier.eid | 2-s2.0-85071687857 | |
| dc.identifier.pmid | 31412687 | |
| dc.identifier.uri | http://hdl.handle.net/10938/29151 | |
| dc.language.iso | en | |
| dc.publisher | MDPI AG | |
| dc.relation.ispartof | Genes | |
| dc.source | Scopus | |
| dc.subject | Drosophila | |
| dc.subject | Eto-1 | |
| dc.subject | Flt3 itd | |
| dc.subject | Idh1/2 | |
| dc.subject | Mice | |
| dc.subject | Npm-1 | |
| dc.subject | Rats | |
| dc.subject | Zebrafish | |
| dc.subject | Animals | |
| dc.subject | Carcinogens | |
| dc.subject | Disease models, animal | |
| dc.subject | Drosophila melanogaster | |
| dc.subject | Leukemia, myeloid, acute | |
| dc.subject | Mutagenesis | |
| dc.subject | Oncogenic viruses | |
| dc.subject | Carcinogen | |
| dc.subject | Acute myeloid leukemia | |
| dc.subject | Animal model | |
| dc.subject | Mouse model | |
| dc.subject | Nod scid gamma mouse | |
| dc.subject | Nonhuman | |
| dc.subject | Pathophysiology | |
| dc.subject | Rat model | |
| dc.subject | Review | |
| dc.subject | Scid mouse | |
| dc.subject | Transgenic mouse | |
| dc.subject | Zebra fish | |
| dc.subject | Animal | |
| dc.subject | Disease model | |
| dc.subject | Mouse | |
| dc.subject | Pathogenicity | |
| dc.subject | Pathology | |
| dc.subject | Rat | |
| dc.subject | Tumor virus | |
| dc.title | A critical review of animal models used in acute myeloid leukemia pathophysiology | |
| dc.type | Review |
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