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First identified and characterized by researchers at the University of Zagreb, BPC-157 has been the subject of extensive preclinical investigation spanning over two decades

This transforms the tumor into a highly vulnerable, biologically primed target, enabling precise, high-effect radiation delivery even in bulky, hypoxic, or treatment-resistant cervical cancers [170]

In contrast, low-affinity interactions, typically requiring micromolar ligand concentrations, often fail to accurately reflect the receptor-ligand dynamics observed within cellular environments

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