Target intelligence / Profile preview

S100 calcium-binding protein A7A (S100A7A)

Target
S100A7A
Molecular classification
Calcium-binding protein, Antimicrobial peptide, Cytokine/chemoattractant-like protein, Other
01

Overview

S100 calcium-binding protein A7A (S100A7A), also known as koebnerisin, is a member of the S100 family of calcium-binding proteins highly expressed in epithelial tissues such as the skin and breast[5]. It plays a role in epithelial homeostasis, innate immunity, and antimicrobial host defense by acting directly as an antimicrobial peptide, especially against *E. coli*[5]. Koebnerisin is overexpressed in inflammatory skin diseases (including psoriasis, where it contributes to the \"Koebner phenomenon\") and certain breast cancers, where its secretion functions as a chemoattractant that enhances inflammation and may drive tumor progression in hormone receptor–negative tumors. S100A7A is closely related at the sequence and functional level to S100A7 (psoriasin), but is distinct in regulation, expression, and function[5]. It acts as a proinflammatory amplifier in the epithelium, attracting myeloid immune cells, and participates in tissue regeneration, maturation, and tumorigenesis in human epithelial tissues[5].

Other names
Protein S100-A7AS100A15S100A7L1S100A7fS100 calcium-binding protein A15S100 calcium-binding protein A7-like 1koebnerisinNICE-2NICE2
02

Mechanism of action

No approved pharmacological agents targeting S100A7A directly\n- As a chemoattractant, S100A7A signals through a Gi protein-coupled receptor (pertussis toxin-sensitive pathway) to attract myeloid leukocytes\n- Contributes to inflammatory amplification with S100A7 via RAGE-dependent mechanisms[5]

03

Biological functions

Antimicrobial host defenseRegulation of cell proliferationRegulation of cell differentiationCell migrationModulation of immune/inflammatory responseEpithelial homeostasisChemoattraction of myeloid leukocytes
04

Disease associations

Inflammation (psoriasis, eczema, other inflammatory skin diseases)Cancer (notably breast cancer; also implicated in epithelial tumorigenesis)Potential roles in infection (as part of antimicrobial defense)Other (Koebner phenomenon in skin)
05

Safety considerations

Lack of pharmacological targeting means therapeutic challenges and safety profile are not establishedOverexpression amplifies inflammation, which may contribute to pathology in chronic inflammatory disease[5]
06

Biomarkers

Overexpression in psoriasis and eczema lesions (inflammatory skin disease biomarker)Overexpression in ER/PR-negative breast cancer (potential tumor progression biomarker)[5]

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