Register for free to
view the full innovation profile.
The novel sequences recognize c-MET with high affinity and are less likely to induce a detrimental immune response in human patients since they are fully human(low immunogenicity).
About
Summary UCLA researchers in the Department of Molecular and Medical Pharmacology have developed several novel recognition sequences against the human oncogene c-MET. These unique sequences are the basic building blocks used to make intact human antibodies and antibody fragments that can be conjugated to various payloads endowing them with great therapeutic and diagnostic potential in vitro and in vivo. Background The proto-oncogene c-MET (hepatocyte growth factor receptor, HGFR) is a membrane-bound tyrosine kinase receptor expressed on the surface of cells of epithelial origin. In normal cells, c-MET signalling is initiated in response to hepatocyte growth factor (HGF), and is responsible for wound healing and tissue regeneration. However, in the case of cancer, this pathway is abnormally activated leading to several biological processes known together as invasive growth. In fact, the c-MET pathway is one of the most frequently dysregulated pathways in human cancer. Aberrant c-MET signalling has been documented in most solid tumours and haematological malignancies, and is tightly associated with the resistance to various cancer therapies. Reflecting their critical roles in cancer development and progression, c-MET and HGF have become leading candidates for targeted cancer therapies and diagnostics. Several mouse c-MET antibodies are available for in vitro use, and a single humanized c-MET antibody is being evaluated for its therapeutic and diagnostic potential. However, there are currently no fully human c-Met antibodies being available for cancer therapeutics or diagnostics. Innovation Dr. Anna Wu and colleagues in UCLA’s Department of Molecular and Medical Pharmacology have developed several novel human recognition sequences against the oncogene c-MET. These sequences are the basic building blocks used to synthesize c-MET-specific intact antibodies and antibody fragments (scFV, diabody, cys-diabody) with varying sizes and pharmacokinetics. The novel sequences recognize c-MET with high affinity (nanomolar/sub-nanomolar) and are less likely to induce a detrimental immune response in human patients since they are fully human (low immunogenicity). Intact antibodies or antibody fragments can be used alone as potential blocking agents or conjugated to several different payloads. Specifically, the formation of cys-diabody fragments allow for site-specific conjugation to various payloads (fluorophores, radioisotopes, nanoparticles, or cytotoxic drugs) making them very convenient reagents for several in vitro and in vivo applications. Researchers have confirmed that the novel recognition sequences have nanomolar affinity for c-MET and are currently testing the utility of these antibody fragments in diagnostic applications. Applications Receptor antagonist In vivo imaging (immunoPET) Targeted drug delivery In vitro diagnosis Circulating tumor cell capture