General Information of the Disease (ID: DIS00010)
Name
Myelodysplastic syndrome
ICD
ICD-11: 2A3Z
Full List of Target(s) of This Ferroptosis-centered Disease
Phospholipid hydroperoxide glutathione peroxidase (GPX4)
In total 1 item(s) under this target
Experiment 1 Reporting the Ferroptosis-centered Disease Response by This Target [1]
Target for Ferroptosis Suppressor
Responsed Disease Myelodysplastic syndrome [ICD-11: 2A3Z]
Responsed Drug Decitabine Investigative
Pathway Response Fatty acid metabolism hsa01212
Ferroptosis hsa04216
Necroptosis hsa04217
Cell Process Cell ferroptosis
Cell necroptosis
In Vitro Model SKM-1 cells Acute myeloid leukemia Homo sapiens CVCL_0098
MUTZ-1 cells Burkitt lymphoma Homo sapiens CVCL_1431
In Vivo Model
C57BL/6 mice were purchased from Vital River (Beijing, China) at 6 to 8 weeks of age. Twenty mice were housed with five individuals per cage and used at a weight of approximately 20.0-22.0 g. They were randomly divided into four groups, five in each group, namely control group, low-dose group, middle-dose group, and high-dose group. The low-, middle-, and high-dose group mice were administered an intraperitoneal injection of 0.2-ml iron dextran at a concentration of 6.25, 12.5, and 25 mg/ml, respectively, every 3 days for 10 weeks to establish iron overload model. At the same time, normal saline was given to the control group.

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Response regulation Ferroptosis may account for the main mechanisms of how decitabine induced death of myelodysplastic syndrome (MDS) cells. Decitabine-induced ROS raise leads to ferroptosis in MDS cells by decreasing GSH level and GPX4 activity.
References
Ref 1 Abnormal Ferroptosis in Myelodysplastic Syndrome. Front Oncol. 2020 Sep 2;10:1656. doi: 10.3389/fonc.2020.01656. eCollection 2020.