Drug intelligence / Profile preview

ANXA7-I1 lentivirus

Development stage
Preclinical
Lead developer
University of Alabama at Birmingham
Modality
Gene Therapies
Administration
Intratumoral
01

Overview

ANXA7-I1 lentivirus is an experimental gene therapy construct designed to overexpress the Annexin A7 isoform 1 (I1) protein, specifically for the treatment of glioblastoma (GBM). In GBM, the Epidermal Growth Factor Receptor (EGFR) often escapes degradation and is recycled to the cell surface, maintaining hyperactive signaling. ANXA7-I1 contains unique tyrosine residues that, when phosphorylated, facilitate the trafficking of EGFR to lysosomes for degradation. Research presented at the Society for Neuro-Oncology (SNO) meetings in 2024 and 2025 demonstrates that lentiviral delivery of ANXA7-I1 in glioma stem cells (GSCs) reduces total and surface EGFR levels, thereby inhibiting downstream signaling. This mechanism represents a potential therapeutic strategy to overcome RTK-driven resistance and reduce the tumorigenicity of GSC populations.

Other names
Annexin A7 isoform 1 lentivirusANXA7 isoform 1 lentivirusANXA-7 isoform 1 lentivirusANXA 7 isoform 1 lentivirus
02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)PDGFRA (Platelet-derived growth factor receptor alpha)MET (Mesenchymal-epithelial transition factor receptor)

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