Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10907322 | Experimental Hematology | 2016 | 6 Pages |
Abstract
Fanconi anemia (FA) is an inherited disorder of genomic instability associated with high risk of myelodysplasia and acute myeloid leukemia (AML). Young mice deficient in FA core complex genes do not naturally develop cancer, hampering preclinical studies on malignant hematopoiesis in FA. Here we describe that aging Fanccâ/â mice are prone to genomically unstable AML and other hematologic neoplasms. We report that aneuploidy precedes malignant transformation during Fanccâ/â hematopoiesis. Our observations reveal that Fanccâ/â mice develop hematopoietic chromosomal instability followed by leukemia in an age-dependent manner, recapitulating the clinical phenotype of human FA and providing a proof of concept for future development of preclinical models of FA-associated leukemogenesis.
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Authors
Donna Cerabona, Zejin Sun, Grzegorz Nalepa,