Immunoglobulin superfamily, WD repeat domain containing (WDR family), Heparin-binding protein, Other (not classified as receptor, enzyme, transporter, etc.)
01
Overview
Angio-associated migratory cell protein (AAMP) is a conserved, immunoglobulin superfamily protein containing a WD40 domain and a heparin-binding site. It is primarily expressed in the cytosol of vascular endothelial cells and certain cancer cells. Its main biological roles include driving angiogenesis and regulating cell migration—which it does via the RhoA/Rho-kinase signaling pathway. AAMP’s expression and function are relevant in numerous disease processes, especially cancer and cardiovascular disease, where abnormal cell migration and blood vessel formation play critical roles. While AAMP is a promising therapeutic target for diseases involving pathological angiogenesis and cell migration, no approved drugs currently target it directly
Other names
AAMPAngio-associated migratory cell proteinAngio associated migratory cell protein
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Mechanism of action
Not established for approved drugs. Mechanistically, targeting AAMP could affect angiogenesis, cell migration, and RhoA pathway modulation
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Biological functions
Angiogenesis (formation of new blood vessels)Cell migration (regulation in endothelial and smooth muscle cells, cytotrophoblasts, cancer cells)Endothelial tube formationHeparin-sensitive cell adhesionRhoA/Rho-kinase pathway signaling (involved in cell migration/division)
Targeting proteins involved in angiogenesis (like AAMP) could potentially affect vascular health and wound healing (class-wide concern for angiogenesis modulators)No specific safety concerns are documented for targeting AAMP directly, as no clinical drugs exist currently
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Interacting drugs
No commonly recognized approved drugs directly targeting AAMP. Some small molecule perturbations that change AAMP expression have been described in high-throughput datasets, but specific drugs are not validated as therapeutic interventions
1 more in the full profile.
07
Biomarkers
AAMP expression has been correlated with disease status and tissue necrosis in situ in conditions such as GIST, ductal carcinomas, and other malignanciesResearch studies use AAMP expression as a marker of endothelial activation or cancer aggressiveness, but it is not widely established as a clinical biomarker
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