Ferroptosis Regulator Information
General Information of the Ferroptosis Regulator (ID: REG10056)
Full List of the Ferroptosis Target of This Regulator and Corresponding Disease/Drug Response(s)
NRAS
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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Unspecific Target [Unspecific Target]
In total 1 item(s) under this target | ||||
Experiment 1 Reporting the Ferroptosis Target of This Regulator | [1] | |||
Responsed Disease | Rhabdomyosarcoma | ICD-11: 2B55 | ||
Pathway Response | Ferroptosis | hsa04216 | ||
MAPK signaling pathway | hsa04010 | |||
PI3K-Akt signaling pathway | hsa04151 | |||
Apoptosis | hsa04210 | |||
Cell Process | Cell ferroptosis | |||
Cell apoptosis | ||||
Cell proliferation | ||||
In Vitro Model |
RMS13 cells | Rhabdomyosarcoma | Mus musculus | CVCL_S112 |
Response regulation | Oncogenic RAS (HRAS, NRAS, KRAS) selectively modulates cell death pathways triggered by cytotoxic stimuli in rhabdomyosarcoma RMS13 cells. In conclusion, our discovery of an increased resistance to oxidative stress imposed by oncogenic RAS mutants in RMS13 cells has important implications for the development of targeted therapies for rhabdomyosarcoma (RMS). | |||
Rhabdomyosarcoma [ICD-11: 2B55]
In total 1 item(s) under this disease | ||||
Experiment 1 Reporting the Ferroptosis-centered Disease Response | [1] | |||
Target Regulator | GTPase NRas (NRAS) | Protein coding | ||
Pathway Response | Ferroptosis | hsa04216 | ||
MAPK signaling pathway | hsa04010 | |||
PI3K-Akt signaling pathway | hsa04151 | |||
Apoptosis | hsa04210 | |||
Cell Process | Cell ferroptosis | |||
Cell apoptosis | ||||
Cell proliferation | ||||
In Vitro Model |
RMS13 cells | Rhabdomyosarcoma | Mus musculus | CVCL_S112 |
Response regulation | Oncogenic RAS (HRAS, NRAS, KRAS) selectively modulates cell death pathways triggered by cytotoxic stimuli in rhabdomyosarcoma RMS13 cells. In conclusion, our discovery of an increased resistance to oxidative stress imposed by oncogenic RAS mutants in RMS13 cells has important implications for the development of targeted therapies for rhabdomyosarcoma (RMS). | |||