Loss of erythroblasts in acute myeloid leukemia causes iron redistribution with clinical implications
Details
Publication Year 2021-08-24,Volume 5,Issue #16,Page 3102-3112
Journal Title
Blood Advances
Abstract
Acute myeloid leukemia (AML) is a heterogeneous disease with poor prognosis and limited treatment strategies. Determining the role of cell-extrinsic regulators of leukemic cells is vital to gain clinical insights into the biology of AML. Iron is a key extrinsic regulator of cancer, but its systemic regulation remains poorly explored in AML. To address this question, we studied iron metabolism in patients with AML at diagnosis and explored the mechanisms involved using the syngeneic MLL-AF9-induced AML mouse model. We found that AML is a disorder with a unique iron profile, not associated with inflammation or transfusion, characterized by high ferritin, low transferrin, high transferrin saturation (TSAT), and high hepcidin. The increased TSAT in particular, contrasts with observations in other cancer types and in anemia of inflammation. Using the MLL-AF9 mouse model of AML, we demonstrated that the AML-induced loss of erythroblasts is responsible for iron redistribution and increased TSAT. We also show that AML progression is delayed in mouse models of systemic iron overload and that elevated TSAT at diagnosis is independently associated with increased overall survival in AML. We suggest that TSAT may be a relevant prognostic marker in AML.
Publisher
ASH
Research Division(s)
Inflammation
PubMed ID
34402883
Open Access at Publisher's Site
https://doi.org/10.1182/bloodadvances.2021004373
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2021-09-17 11:04:11
Last Modified: 2021-09-17 11:13:48
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