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GBM-IC2 is a targeting peptide identified through in vivo phage display biopanning that specifically binds to N-cadherin (CDH2) on glioma stem cells (GSCs). Developed by researchers at the Moffitt Cancer Center, the peptide was selected for its ability to bind specifically to GSCs in vitro and glioblastoma (GBM) tissue in vivo. N-cadherin is a surface receptor associated with self-renewal and tumor recapitulation in glioma, making it a potential marker for treatment-resistant cell populations. GBM-IC2 is being investigated as a vehicle for targeted therapeutic delivery or as a diagnostic tool for identifying aggressive cell populations within brain tumors.
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