Target intelligence / Profile preview

Cysteine dioxygenase type 1 (CDO1)

Target
CDO1
Molecular classification
Enzyme, Iron-containing metalloenzyme, Non-heme Fe(II) dioxygenase
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Overview

Cysteine dioxygenase type 1 (CDO1) is a non-heme, iron-dependent enzyme that catalyzes the first and rate-limiting step of cysteine catabolism, converting cysteine to cysteine sulfinic acid—a precursor in taurine and sulfate metabolism. CDO1 is tightly regulated and essential for controlling intracellular cysteine levels and redox balance. Dysregulation or epigenetic silencing of CDO1 is frequently observed in multiple cancers, correlating with tumor progression, poor prognosis, and altered chemotherapeutic response. Beyond cancer, CDO1 is implicated in lipid metabolism, redox homeostasis, neurodegenerative diseases, and other metabolic and developmental processes. CDO1 is thus a biologically significant enzyme and a promising diagnostic and prognostic biomarker, though not yet a direct drug target in clinical therapeutics

Other names
CDOCDO-ICysteine dioxygenase type Icysteine dioxygenase, type ICDO1
02

Mechanism of action

Enzyme inhibition (potential mechanism for experimental compounds; currently not clinically targeted) Epigenetic modulation (biomodulators, e.g., demethylating agents, could restore CDO1 expression in cancer models, but these are not specific drugs for CDO1)

03

Biological functions

Cysteine catabolismRegulation of intracellular cysteine levelsRedox homeostasisTaurine biosynthesisLipid metabolismAdipogenesisOsteoblastic differentiationBile acid metabolismSulfide metabolismRegulation of cellular metabolism and ROS (reactive oxygen species) balanceControl of organismal growth and development
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Disease associations

Cancer (e.g., tumor suppressor role, epigenetically silenced in various cancers)Metabolic disordersNeurodegenerative diseases (e.g., Alzheimer's disease, Parkinson's disease, motor neuron disease)Rheumatoid arthritis
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Safety considerations

Risk of altered cysteine and redox balance with inhibition/modulationPotential impact on systemic taurine, sulfate, and lipid metabolism, which could affect multiple organs
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Biomarkers

CDO1 promoter methylation (cancer biomarker for colorectal, breast, lung, esophageal, bladder, and stomach cancer)CDO1 gene expression (tumor progression and prognosis, responsiveness to therapy)

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