Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B96b42790d9344bad6f618234302a59ec> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B96b42790d9344bad6f618234302a59ec NCIT_P378 "NCI" @default.
- B96b42790d9344bad6f618234302a59ec type Axiom @default.
- B96b42790d9344bad6f618234302a59ec annotatedProperty IAO_0000115 @default.
- B96b42790d9344bad6f618234302a59ec annotatedSource NCIT_C100101 @default.
- B96b42790d9344bad6f618234302a59ec annotatedTarget "An immunoconjugate that consists of a humanized IgG1 antibody K7153A against the cell-surface antigen CD37 and covalently linked via the uncleavable, maleimide-derived thioether-based linker SMCC to the maytansinoid DM1, with potential pro-apoptotic and cytotoxic activities. Upon administration of naratuximab emtansine, the antibody moiety of IMGN529 binds to CD37 on tumor B-cells and induces an antibody-dependent cell-mediated cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC), thereby showing pro-apoptotic activity. In addition, after the internalization of this agent and lysosomal degradation, the DM1 moiety binds to tubulin and inhibits tubulin polymerization and microtubule assembly, resulting in a disruption of microtubule activity and cell division, and eventually causing cell death in CD37-positive B-cells. CD37, a transmembrane glycoprotein, is overexpressed in B-cell malignancies. Compared to reducible, cleavable linkers, the non-reducible SMCC linker shows increased stability in plasma." @default.