Researchers at the University of California, Davis have developed a unique non-sacrificial synthetic peptide substrate designed to inhibit plasmin activity and prevent tumor progression and ascites formation in cancers characterized by elevated plasmin levels.
This technology relates to a synthetic peptide engineered from bovine pancreatic trypsin inhibitor (BPTI). Since all peptide-based plasmin inhibitors are sacrificial substrates for plasmin cleavage , this invention is designed to resist proteolytic degradation by plasmin. This highly stable peptide is resistant to plasmin even after 48 hours of incubation and significantly efficacious over BPTI against ascites development in xenograft models. The peptide may be fused to targeting moieties such as antibodies specific to tumor-associated antigens (e.g., folate receptor alpha or Fas receptor). It is designed to treat tumors characterized by elevated plasmin levels, including ovarian, breast, and pancreatic cancers, and to prevent malignant ascites formation. Additionally, it may be used to reduce bleeding during heart surgeries like coronary artery bypass.
antibody, ascites, cancer, chemotherapy, immunotherapy, peptide, plasmin, solid tumor, synthetic peptide, tumor-associated antigen