General Information of the Ferroptosis Regulator (ID: REG30010)
Regulator Name CERS6-AS1 (IncRNA)
Synonyms
CERS6-AS1
    Click to Show/Hide
Gene Name CERS6-AS1
Gene ID 100861402
Regulator Type lncRNA
Ensembl ID ENSG00000227617
HGNC ID
HGNC:44485
Full List of the Ferroptosis Target of This Regulator and Corresponding Disease/Drug Response(s)
CERS6-AS1 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).
Browse Target
Browse Disease
Cystine/glutamate transporter (SLC7A11) [Driver; 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 Thyroid cancer ICD-11: 2D10
Pathway Response Ferroptosis hsa04216
Cell Process Cell ferroptosis
Cell proliferation
In Vitro Model
Nthy-ori3-1 cells Normal Homo sapiens CVCL_2659
IHH-4 cells Thyroid gland papillary carcinoma Homo sapiens CVCL_2960
BCPAP cells Thyroid carcinoma Homo sapiens CVCL_0153
KTC-1 cells Thyroid carcinoma Homo sapiens CVCL_6300
TPC-1 cells Thyroid gland papillary carcinoma Homo sapiens CVCL_6298
In Vivo Model
Animal experiments were approved by ethics committee of Wuzhou Red Cross Hospital. The TPC-1 cells transfected with sh-CERS6-AS1 or sh-NC were made into cell suspension (2 x 106/ml) with PBS. Then nude mice were randomly divided into sh-CERS6-AS1 group (n = 6) and sh-NC group (n = 6). The mice were subcutaneously inoculated with 200 ul corresponding cell suspension respectively, and then the weight and tumor volume of mice were recorded every other week. After 5 weeks, pentobarbital sodium (120 mg/kg) were intraperitoneally injected to make nude mice euthanasia, and then the tumors were stripped and weighed. Subsequently, immunohistochemistry and RT-PCR were performed.

    Click to Show/Hide
Response regulation Silencing CERS6-AS1 suppressed cell viability and increased ferroptosis in papillary thyroid cancer. LASP1 was modulated by CERS6-AS1 through sponging miR-497-5p. The expression of Ki67, PCNA, GPX4, and SLC7A11 was inhibited by si- CERS6-AS1 transfection.
Thyroid cancer [ICD-11: 2D10]
In total 1 item(s) under this disease
Experiment 1 Reporting the Ferroptosis-centered Disease Response [1]
Target Regulator CERS6-AS1 (IncRNA) lncRNA
Pathway Response Ferroptosis hsa04216
Cell Process Cell ferroptosis
Cell proliferation
In Vitro Model
Nthy-ori3-1 cells Normal Homo sapiens CVCL_2659
IHH-4 cells Thyroid gland papillary carcinoma Homo sapiens CVCL_2960
BCPAP cells Thyroid carcinoma Homo sapiens CVCL_0153
KTC-1 cells Thyroid carcinoma Homo sapiens CVCL_6300
TPC-1 cells Thyroid gland papillary carcinoma Homo sapiens CVCL_6298
In Vivo Model
Animal experiments were approved by ethics committee of Wuzhou Red Cross Hospital. The TPC-1 cells transfected with sh-CERS6-AS1 or sh-NC were made into cell suspension (2 x 106/ml) with PBS. Then nude mice were randomly divided into sh-CERS6-AS1 group (n = 6) and sh-NC group (n = 6). The mice were subcutaneously inoculated with 200 ul corresponding cell suspension respectively, and then the weight and tumor volume of mice were recorded every other week. After 5 weeks, pentobarbital sodium (120 mg/kg) were intraperitoneally injected to make nude mice euthanasia, and then the tumors were stripped and weighed. Subsequently, immunohistochemistry and RT-PCR were performed.

    Click to Show/Hide
Response regulation Silencing CERS6-AS1 suppressed cell viability and increased ferroptosis in papillary thyroid cancer. LASP1 was modulated by CERS6-AS1 through sponging miR-497-5p. The expression of Ki67, PCNA, GPX4, and SLC7A11 was inhibited by si- CERS6-AS1 transfection.
References
Ref 1 CERS6-AS1 Facilitates Oncogenesis and Restrains Ferroptosis in Papillary Thyroid Carcinoma by Serving as a ceRNA through miR-497-5p/LASP1 Axis. Ann Clin Lab Sci. 2022 May;52(3):426-438.