Target intelligence / Profile preview

Tenascin-C protein (TNC)

Target
TNC
Molecular classification
Matricellular protein, Extracellular matrix glycoprotein, Other
01

Overview

Tenascin-C protein (TNC) is a large, hexameric, and multimodular extracellular matrix glycoprotein encoded by the TNC gene on chromosome 9. It is primarily classified as a matricellular protein, meaning it modulates cell-matrix interactions rather than providing mere structural support. Tenascin-C is mostly absent in healthy adult tissues but is highly expressed during embryogenesis, tissue injury, inflammation, infection, and particularly in the microenvironment of various cancers, such as glioma. Functionally, it regulates cellular proliferation, differentiation, migration, survival, and apoptosis, and remodels the tissue microenvironment partly by interacting with integrins, growth factor receptors, and a broad range of extracellular partners. In pathological contexts, upregulation of TNC is linked to tumor progression, poor clinical outcomes, and altered responses to inflammation and infection. While there are no approved drugs directly targeting TNC, it is widely investigated as a disease biomarker and potential therapeutic target, especially in oncology and regenerative medicine

Other names
cytotactinhexabrachionglial/mesenchymal extracellular matrix protein (GMEM)neuronectinJ1 220/200myotendinous antigenTENA
02

Mechanism of action

Not directly targeted by drugs as a classical receptor or enzyme. However, TNC modulates cellular responses via binding to integrins, EGF receptor, Toll-like receptor 4, and interaction with growth factors, affecting cell signaling, immune response, and tissue remodeling

03

Biological functions

Regulation of cell proliferationRegulation of cell migrationApoptosisTissue remodelingCell differentiationSynaptic plasticityGuidance of migrating neurons and axons during developmentImmune response modulation
04

Disease associations

Cancer (notably glioma and other solid tumors)InflammationInfectious disease (including HIV-1 interactions)Cardiovascular disease (involvement in vessel development and pathology)
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Safety considerations

Upregulation in cancer and pathological tissue remodeling may contribute to disease progression and poor prognosis if targeted non-selectivelyAs a diagnostic/prognostic biomarker, tissue- and context-specific expression must be considered to avoid misinterpretation
06

Interacting drugs

None with established direct pharmacological intervention reported as of the latest literature; mainly studied as a disease marker or biological modulator rather than a direct drug target
07

Biomarkers

Biomarker for tumor progression, particularly in glioma and various solid cancersBiomarker for tissue injury, pathogenic remodeling, and inflammation

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