Ferroptosis Regulator Information
General Information of the Ferroptosis Regulator (ID: REG50008)
Full List of the Ferroptosis Target of This Regulator and Corresponding Disease/Drug Response(s)
hsa-mir-222
can regulate the following target(s), and cause disease/drug response(s). You can browse detail information of target(s) or disease/drug response(s).
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Transferrin receptor protein 1 (TFRC) [Driver; Suppressor; Marker]
In total 1 item(s) under this target | |||||
Experiment 1 Reporting the Ferroptosis Target of This Regulator | [1] | ||||
Target for Ferroptosis | Marker/Suppressor/Driver | ||||
Responsed Disease | Liver fibrosis | ICD-11: DB93 | |||
Pathway Response | Fatty acid metabolism | hsa01212 | |||
Ferroptosis | hsa04216 | ||||
Cell Process | Cell ferroptosis | ||||
Cell proliferation | |||||
In Vitro Model |
L-02 cells | Endocervical adenocarcinoma | Homo sapiens | CVCL_6926 | |
In Vivo Model |
Male C57BL/6 mice (6-8-weeks old; Vitalriver, Beijing, China) were employed. Briefly, 200 ul AAV8-HBV-1.2 was introduced through the tail vein. The exosomes (10 ug) derived from HBV-infected LO2 cells were dissolved in PBS (50 ul) and introduced through the tail vein 2 h after AAV8-HBV-1.2 injection. Mice were anesthetized by inhalation with 3% isoflurane and sacrificed by cervical dislocation after 4 weeks to collect livers for hematoxylin-eosin (HE) and Masson's Trichrome staining and measurement of liver injury as previously described.
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Response regulation | Exosomes derived from HBV-infected LO2 cells promote LX-2 cell activation and liver fibrosis in mouse Exosomal miR-222 derived from HBV-infected LO2 cells promotes LX-2 cell activation TFRC is a target of miR-222 and inhibits LX-2 cell activation induced by miR-222 miR-222 promotes LX-2 cell activation through inhibiting TFRC-induced ferroptosis. | ||||
Liver fibrosis [ICD-11: DB93]
In total 1 item(s) under this disease | |||||
Experiment 1 Reporting the Ferroptosis-centered Disease Response | [1] | ||||
Target Regulator | hsa-mir-222 (Precursor RNA) | Precursor RNA | |||
Pathway Response | Fatty acid metabolism | hsa01212 | |||
Ferroptosis | hsa04216 | ||||
Cell Process | Cell ferroptosis | ||||
Cell proliferation | |||||
In Vitro Model |
L-02 cells | Endocervical adenocarcinoma | Homo sapiens | CVCL_6926 | |
In Vivo Model |
Male C57BL/6 mice (6-8-weeks old; Vitalriver, Beijing, China) were employed. Briefly, 200 ul AAV8-HBV-1.2 was introduced through the tail vein. The exosomes (10 ug) derived from HBV-infected LO2 cells were dissolved in PBS (50 ul) and introduced through the tail vein 2 h after AAV8-HBV-1.2 injection. Mice were anesthetized by inhalation with 3% isoflurane and sacrificed by cervical dislocation after 4 weeks to collect livers for hematoxylin-eosin (HE) and Masson's Trichrome staining and measurement of liver injury as previously described.
Click to Show/Hide
|
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Response regulation | Exosomes derived from HBV-infected LO2 cells promote LX-2 cell activation and liver fibrosis in mouse Exosomal miR-222 derived from HBV-infected LO2 cells promotes LX-2 cell activation TFRC is a target of miR-222 and inhibits LX-2 cell activation induced by miR-222 miR-222 promotes LX-2 cell activation through inhibiting TFRC-induced ferroptosis. | ||||