General Information of the Ferroptosis Regulator (ID: REG10236)
Regulator Name Cysteine dioxygenase type 1 (CDO1)
Synonyms
Cysteine dioxygenase type I
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Gene Name CDO1
Gene ID 1036
Regulator Type Protein coding
Uniprot ID Q16878
Sequence
MEQTEVLKPRTLADLIRILHQLFAGDEVNVEEVQAIMEAYESDPTEWAMYAKFDQYRYTR
NLVDQGNGKFNLMILCWGEGHGSSIHDHTNSHCFLKMLQGNLKETLFAWPDKKSNEMVKK
SERVLRENQCAYINDSIGLHRVENISHTEPAVSLHLYSPPFDTCHAFDQRTGHKNKVTMT
FHSKFGIRTPNATSGSLENN

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Family Cysteine dioxygenase family
Function
Catalyzes the oxidation of cysteine to cysteine sulfinic acid with addition of molecular dioxygen.

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HGNC ID
HGNC:1795
KEGG ID hsa:1036
Full List of the Ferroptosis Target of This Regulator and Corresponding Disease/Drug Response(s)
CDO1 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
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 Gastric cancer ICD-11: 2B72
Pathway Response Fatty acid metabolism hsa01212
Ferroptosis hsa04216
Cell Process Cell ferroptosis
Cell proliferation
In Vitro Model
AGS cells Gastric adenocarcinoma Homo sapiens CVCL_0139
BGC-823 cells Gastric carcinoma Homo sapiens CVCL_3360
MKN45 cells Gastric adenocarcinoma Homo sapiens CVCL_0434
SGC-7901 cells Gastric carcinoma Homo sapiens CVCL_0520
MGC-803 cells Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
In Vivo Model
1 x 106 BGC823 control or CDO1 short hairpin (sh)RNA treated cells in 150 ul PBS were injected subcutaneously right of the dorsal midline in athymic nude mice. Once the tumors reached 80 to 100 mm3 at day 10, mice were allocated randomly into groups of five and treated with erastin (30 mg/kg intraperitoneally, twice every other day).

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Response regulation Silencing CDO1 inhibited erastin-induced ferroptosis in gastric cancer cells both in vitro and in vivo. Mechanistically, c-Myb transcriptionally regulated CDO1, and inhibition of CDO1 expression upregulated GPX4 expression.
Gastric cancer [ICD-11: 2B72]
In total 1 item(s) under this disease
Experiment 1 Reporting the Ferroptosis-centered Disease Response [1]
Target Regulator Cysteine dioxygenase type 1 (CDO1) Protein coding
Pathway Response Fatty acid metabolism hsa01212
Ferroptosis hsa04216
Cell Process Cell ferroptosis
Cell proliferation
In Vitro Model
AGS cells Gastric adenocarcinoma Homo sapiens CVCL_0139
BGC-823 cells Gastric carcinoma Homo sapiens CVCL_3360
MKN45 cells Gastric adenocarcinoma Homo sapiens CVCL_0434
SGC-7901 cells Gastric carcinoma Homo sapiens CVCL_0520
MGC-803 cells Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
In Vivo Model
1 x 106 BGC823 control or CDO1 short hairpin (sh)RNA treated cells in 150 ul PBS were injected subcutaneously right of the dorsal midline in athymic nude mice. Once the tumors reached 80 to 100 mm3 at day 10, mice were allocated randomly into groups of five and treated with erastin (30 mg/kg intraperitoneally, twice every other day).

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Response regulation Silencing CDO1 inhibited erastin-induced ferroptosis in gastric cancer cells both in vitro and in vivo. Mechanistically, c-Myb transcriptionally regulated CDO1, and inhibition of CDO1 expression upregulated GPX4 expression.
References
Ref 1 Cysteine Dioxygenase 1 Mediates Erastin-Induced Ferroptosis in Human Gastric Cancer Cells. Neoplasia. 2017 Dec;19(12):1022-1032. doi: 10.1016/j.neo.2017.10.005. Epub 2017 Nov 13.