Target intelligence / Profile preview

Cystatin C (CST3)

Target
CST3
Molecular classification
Cysteine protease inhibitor, Type 2 cystatin, Protein (secreted, extracellular)
01

Overview

Cystatin C is a small, non-glycosylated protein of 120 amino acids (~13 kDa) encoded by the CST3 gene, widely expressed and secreted by all nucleated human cells[1][5][6]. It is the principal extracellular inhibitor of cysteine proteases, especially cathepsins, helping regulate proteolytic processes in tissues and bodily fluids[1][5][3]. Cystatin C provides cell and tissue protection by controlling protease activity during inflammation, tissue remodeling, and apoptotic events[2][1][5]. Highest physiological concentrations are found in cerebrospinal fluid, semen, breastmilk, tears, and saliva[1][6]. Its serum levels are used clinically to assess kidney function, being less influenced by muscle mass than creatinine, and altered levels may indicate risk for cardiovascular and neurodegenerative disease. Mutations or aggregation of Cystatin C are associated with rare hereditary amyloid disorders and may play a role in the pathogenesis of Alzheimer's disease and cerebral vessel fragility[3][2][4][6].

Other names
Cystatin-3Gamma-traceNeuroendocrine basic polypeptidePost-gamma-globulinADLDWAARMD11HEL-S-2cystatin-CbA218C14.4epididymis secretory protein Li 2CST3
02

Mechanism of action

Endogenous inhibitor: Prevents proteolysis by binding and inhibiting cysteine proteases (cathepsins)[1][3][6].

03

Biological functions

Inhibition of cysteine proteases (notably cathepsins B, H, L)Regulation of protease activity in extracellular and intracellular environmentsModulation of immune responseInvolvement in neuroprotectionHomeostasis of extracellular matrix
04

Disease associations

Chronic kidney disease (as a biomarker)Cardiovascular diseaseCerebral amyloid angiopathyAlzheimer’s diseaseAge-related macular degenerationAtherosclerosisNeurodegenerative disease
05

Safety considerations

No major safety concerns for use as a biomarker; loss of function (e.g., due to protein aggregation) may contribute to amyloid pathology or vessel fragility in disease[4][2][3].
06

Interacting drugs

No approved or widely used drugs are known to directly target Cystatin C, but it is frequently measured as a biomarker; some experimental agents may modulate cathepsin activity indirectly linked to Cystatin C pathways[1][5][3].
07

Biomarkers

Serum or plasma Cystatin C levels (for kidney function assessment and cardiovascular risk prediction)[1][3]Cerebrospinal fluid Cystatin C levels (for neurodegenerative disease studies)[2][6]

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