Ferroptosis Regulator Information
General Information of the Ferroptosis Regulator (ID: REG30038)
Full List of the Ferroptosis Target of This Regulator and Corresponding Disease/Drug Response(s)
LINC00239
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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Phospholipid hydroperoxide glutathione peroxidase (GPX4) [Suppressor]
In total 1 item(s) under this target | |||||
Experiment 1 Reporting the Ferroptosis Target of This Regulator | [1] | ||||
Target for Ferroptosis | Suppressor | ||||
Responsed Disease | Colorectal cancer | ICD-11: 2B91 | |||
Pathway Response | Pathways in cancer | hsa05200 | |||
Ferroptosis | hsa04216 | ||||
Cell Process | Cell ferroptosis | ||||
In Vitro Model |
RKO cells | Colon carcinoma | Homo sapiens | CVCL_0504 | |
HCT 116 cells | Colon carcinoma | Homo sapiens | CVCL_0291 | ||
Caco-2 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0025 | ||
SW480 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0546 | ||
SW620 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0547 | ||
FHC cells | Normal | Homo sapiens | CVCL_3688 | ||
In Vivo Model |
To clarify the role of LINC00239 in vivo, we used 4-week-old male BALB/c nude mice provided by the Experimental Animal Center of the Air Force Military Medical University. HCT116 or SW620 cells (1 x 107 cells) were injected subcutaneously into the right flanks of these mice to establish a CRC xenograft model. One week after the injection of cells, the volume of xenografts was continuously monitored (once a week). Four weeks later, the xenografts were removed, and the weights were measured.
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Response regulation | LINC00239 plays a novel and indispensable role in ferroptosis by nucleotides 1-315 of LINC00239 to interact with the Kelch domain (Nrf2-binding site) of Keap1, inhibiting Nrf2 ubiquitination and increasing Nrf2 protein stability. And LINC00239 expression has a positive correlation with Nrf2 and GPX4 expression in colorectal cancer tissues. LINC00239 inhibition in combination with ferroptosis induction might be a promising therapeutic strategy for CRC patients. | ||||
Nuclear factor erythroid 2-related factor 2 (NFE2L2) [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 | ||||
Responsed Disease | Colorectal cancer | ICD-11: 2B91 | |||
Pathway Response | Pathways in cancer | hsa05200 | |||
Ferroptosis | hsa04216 | ||||
Cell Process | Cell ferroptosis | ||||
In Vitro Model |
RKO cells | Colon carcinoma | Homo sapiens | CVCL_0504 | |
HCT 116 cells | Colon carcinoma | Homo sapiens | CVCL_0291 | ||
Caco-2 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0025 | ||
SW480 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0546 | ||
SW620 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0547 | ||
FHC cells | Normal | Homo sapiens | CVCL_3688 | ||
In Vivo Model |
To clarify the role of LINC00239 in vivo, we used 4-week-old male BALB/c nude mice provided by the Experimental Animal Center of the Air Force Military Medical University. HCT116 or SW620 cells (1 x 107 cells) were injected subcutaneously into the right flanks of these mice to establish a CRC xenograft model. One week after the injection of cells, the volume of xenografts was continuously monitored (once a week). Four weeks later, the xenografts were removed, and the weights were measured.
Click to Show/Hide
|
||||
Response regulation | LINC00239 plays a novel and indispensable role in ferroptosis by nucleotides 1-315 of LINC00239 to interact with the Kelch domain (Nrf2-binding site) of Keap1, inhibiting Nrf2 ubiquitination and increasing Nrf2 protein stability. And LINC00239 expression has a positive correlation with Nrf2 and GPX4 expression in CRC tissues. LINC00239 inhibition in combination with ferroptosis induction might be a promising therapeutic strategy for colorectal cancer patients. | ||||
Colorectal cancer [ICD-11: 2B91]
In total 2 item(s) under this disease | |||||
Experiment 1 Reporting the Ferroptosis-centered Disease Response | [1] | ||||
Target Regulator | LINC00239 (IncRNA) | lncRNA | |||
Pathway Response | Pathways in cancer | hsa05200 | |||
Ferroptosis | hsa04216 | ||||
Cell Process | Cell ferroptosis | ||||
In Vitro Model |
RKO cells | Colon carcinoma | Homo sapiens | CVCL_0504 | |
HCT 116 cells | Colon carcinoma | Homo sapiens | CVCL_0291 | ||
Caco-2 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0025 | ||
SW480 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0546 | ||
SW620 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0547 | ||
FHC cells | Normal | Homo sapiens | CVCL_3688 | ||
In Vivo Model |
To clarify the role of LINC00239 in vivo, we used 4-week-old male BALB/c nude mice provided by the Experimental Animal Center of the Air Force Military Medical University. HCT116 or SW620 cells (1 x 107 cells) were injected subcutaneously into the right flanks of these mice to establish a CRC xenograft model. One week after the injection of cells, the volume of xenografts was continuously monitored (once a week). Four weeks later, the xenografts were removed, and the weights were measured.
Click to Show/Hide
|
||||
Response regulation | LINC00239 plays a novel and indispensable role in ferroptosis by nucleotides 1-315 of LINC00239 to interact with the Kelch domain (Nrf2-binding site) of Keap1, inhibiting Nrf2 ubiquitination and increasing Nrf2 protein stability. And LINC00239 expression has a positive correlation with Nrf2 and GPX4 expression in colorectal cancer tissues. LINC00239 inhibition in combination with ferroptosis induction might be a promising therapeutic strategy for CRC patients. | ||||
Experiment 2 Reporting the Ferroptosis-centered Disease Response | [1] | ||||
Target Regulator | LINC00239 (IncRNA) | lncRNA | |||
Pathway Response | Pathways in cancer | hsa05200 | |||
Ferroptosis | hsa04216 | ||||
Cell Process | Cell ferroptosis | ||||
In Vitro Model |
RKO cells | Colon carcinoma | Homo sapiens | CVCL_0504 | |
HCT 116 cells | Colon carcinoma | Homo sapiens | CVCL_0291 | ||
Caco-2 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0025 | ||
SW480 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0546 | ||
SW620 cells | Colon adenocarcinoma | Homo sapiens | CVCL_0547 | ||
FHC cells | Normal | Homo sapiens | CVCL_3688 | ||
In Vivo Model |
To clarify the role of LINC00239 in vivo, we used 4-week-old male BALB/c nude mice provided by the Experimental Animal Center of the Air Force Military Medical University. HCT116 or SW620 cells (1 x 107 cells) were injected subcutaneously into the right flanks of these mice to establish a CRC xenograft model. One week after the injection of cells, the volume of xenografts was continuously monitored (once a week). Four weeks later, the xenografts were removed, and the weights were measured.
Click to Show/Hide
|
||||
Response regulation | LINC00239 plays a novel and indispensable role in ferroptosis by nucleotides 1-315 of LINC00239 to interact with the Kelch domain (Nrf2-binding site) of Keap1, inhibiting Nrf2 ubiquitination and increasing Nrf2 protein stability. And LINC00239 expression has a positive correlation with Nrf2 and GPX4 expression in CRC tissues. LINC00239 inhibition in combination with ferroptosis induction might be a promising therapeutic strategy for colorectal cancer patients. | ||||