Ferroptosis-centered Disease Response Information
General Information of the Disease (ID: DIS00055)
Name |
Hemochromatosis
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ICD |
ICD-11: 3B10-3B11
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Full List of Target(s) of This Ferroptosis-centered Disease
Unspecific Target
In total 1 item(s) under this target | |||||
Experiment 1 Reporting the Ferroptosis-centered Disease Response by This Target | [1] | ||||
Responsed Disease | Hemochromatosis [ICD-11: 3B10-3B11] | ||||
Responsed Drug | Auranofin | Investigative | |||
Responsed Regulator | Thioredoxin reductase 2, mitochondrial (TXNRD2) | Suppressor | |||
Pathway Response | JAK-STAT signaling pathway | hsa04630 | |||
NF-kappa B signaling pathway | hsa04064 | ||||
Fatty acid metabolism | hsa01212 | ||||
Ferroptosis | hsa04216 | ||||
Cell Process | Cell ferroptosis | ||||
In Vitro Model | Huh-7 cells | Hepatocellular carcinoma | Homo sapiens | CVCL_0336 | |
HEK-293T cells | Normal | Homo sapiens | CVCL_0063 | ||
In Vivo Model |
C57BL/6J mice (7-8 weeks of age, both males and females) were purchased from Vital River Laboratory Animal Technology Co., Ltd., Beijing, China. Hfe-/-mice were kindly provided by Dr. Nancy C. Andrews. All mice were housed in a specific pathogen-free facility and fed an egg white-based AIN-76A diet containing 50 mg/kg iron (Research Diets, Inc., New Brunswick, NJ).
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Response regulation | High-dose auranofin (AUR) induces ferroptosis and causes lipid peroxidation through inhibition of thioredoxin reductase (TXNRD) activity.In conclusion, TXNRD is a key regulator of ferroptosis, and AUR is a novel activator of hepcidin and ferroptosis via distinct mechanisms, suggesting a promising approach for treating hemochromatosis and hepcidin-deficiency related disorders. | ||||