Ferroptosis Regulator Information
General Information of the Ferroptosis Regulator (ID: REG10023)
Full List of the Ferroptosis Target of This Regulator and Corresponding Disease/Drug Response(s)
BCAT2
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 | Pancreatic cancer | ICD-11: 2C10 | |||
Responsed Drug | Erastin | Investigative | |||
Pathway Response | Fatty acid metabolism | hsa01212 | |||
Ferroptosis | hsa04216 | ||||
Autophagy | hsa04140 | ||||
Cell Process | Cell ferroptosis | ||||
Cell autophagy | |||||
In Vitro Model |
AsPC-1 cells | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0152 | |
Hep-G2 cells | Hepatoblastoma | Homo sapiens | CVCL_0027 | ||
Panc02 cells | Pancreatic ductal adenocarcinoma | Mus musculus | CVCL_D627 | ||
H22 cells | Hepatoma | Mus musculus | CVCL_H613 | ||
HT-1080 cells | Fibrosarcoma | Homo sapiens | CVCL_0317 | ||
SW480 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0546 | ||
In Vivo Model |
1 x 106 BCAT2 overexpression and control Panc02 cancer cells were implanted subcutaneously into the right dorsal flanks of C57BL/6 mice (five mice per group), respectively. To investigate the role of combination sorafenib with sulfasalazine inducing ferroptosis, 1 x 106 Panc02 were implanted subcutaneously into the right dorsal flanks of C57BL/6 mice. To generate orthotopic tumors, forty C57BL/6 mice were surgically implanted with 1 x 106 H22 cells into left lobe of livers.
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Response regulation | Ferroptosis inducers (erastin, sorafenib, or sulfasalazine) activate ferritinophagy and AMPK phosphorylation, which consequently suppresses nuclear translocation of SREBP1, and inhibits the transcription of its direct target gene BCAT2. BCAT2 is a suppressor of ferroptosis by regulating intracellular glutamate levels in pancreatic ductal adenocarcinoma cells. | ||||
Pancreatic cancer [ICD-11: 2C10]
In total 1 item(s) under this disease | |||||
Experiment 1 Reporting the Ferroptosis-centered Disease Response | [1] | ||||
Target Regulator | Branched-chain-amino-acid aminotransferase, mitochondrial (BCAT2) | Protein coding | |||
Responsed Drug | Erastin | Investigative | |||
Pathway Response | Fatty acid metabolism | hsa01212 | |||
Ferroptosis | hsa04216 | ||||
Autophagy | hsa04140 | ||||
Cell Process | Cell ferroptosis | ||||
Cell autophagy | |||||
In Vitro Model |
AsPC-1 cells | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0152 | |
Hep-G2 cells | Hepatoblastoma | Homo sapiens | CVCL_0027 | ||
Panc02 cells | Pancreatic ductal adenocarcinoma | Mus musculus | CVCL_D627 | ||
H22 cells | Hepatoma | Mus musculus | CVCL_H613 | ||
HT-1080 cells | Fibrosarcoma | Homo sapiens | CVCL_0317 | ||
SW480 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0546 | ||
In Vivo Model |
1 x 106 BCAT2 overexpression and control Panc02 cancer cells were implanted subcutaneously into the right dorsal flanks of C57BL/6 mice (five mice per group), respectively. To investigate the role of combination sorafenib with sulfasalazine inducing ferroptosis, 1 x 106 Panc02 were implanted subcutaneously into the right dorsal flanks of C57BL/6 mice. To generate orthotopic tumors, forty C57BL/6 mice were surgically implanted with 1 x 106 H22 cells into left lobe of livers.
Click to Show/Hide
|
||||
Response regulation | Ferroptosis inducers (erastin, sorafenib, or sulfasalazine) activate ferritinophagy and AMPK phosphorylation, which consequently suppresses nuclear translocation of SREBP1, and inhibits the transcription of its direct target gene BCAT2. BCAT2 is a suppressor of ferroptosis by regulating intracellular glutamate levels in pancreatic ductal adenocarcinoma cells. | ||||
Erastin
[Investigative]
In total 1 item(s) under this drug | |||||
Experiment 1 Reporting the Ferroptosis-centered Drug Response | [1] | ||||
Drug for Ferroptosis | Inducer | ||||
Response Target | Unspecific Target | ||||
Responsed Disease | Pancreatic cancer | ICD-11: 2C10 | |||
Pathway Response | Fatty acid metabolism | hsa01212 | |||
Ferroptosis | hsa04216 | ||||
Autophagy | hsa04140 | ||||
Cell Process | Cell ferroptosis | ||||
Cell autophagy | |||||
In Vitro Model |
AsPC-1 cells | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0152 | |
Hep-G2 cells | Hepatoblastoma | Homo sapiens | CVCL_0027 | ||
Panc02 cells | Pancreatic ductal adenocarcinoma | Mus musculus | CVCL_D627 | ||
H22 cells | Hepatoma | Mus musculus | CVCL_H613 | ||
HT-1080 cells | Fibrosarcoma | Homo sapiens | CVCL_0317 | ||
SW480 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0546 | ||
In Vivo Model |
1 x 106 BCAT2 overexpression and control Panc02 cancer cells were implanted subcutaneously into the right dorsal flanks of C57BL/6 mice (five mice per group), respectively. To investigate the role of combination sorafenib with sulfasalazine inducing ferroptosis, 1 x 106 Panc02 were implanted subcutaneously into the right dorsal flanks of C57BL/6 mice. To generate orthotopic tumors, forty C57BL/6 mice were surgically implanted with 1 x 106 H22 cells into left lobe of livers.
Click to Show/Hide
|
||||
Response regulation | Ferroptosis inducers (erastin, sorafenib, or sulfasalazine) activate ferritinophagy and AMPK phosphorylation, which consequently suppresses nuclear translocation of SREBP1, and inhibits the transcription of its direct target gene BCAT2. BCAT2 is a suppressor of ferroptosis by regulating intracellular glutamate levels in pancreatic ductal adenocarcinoma cells. | ||||