| Literature DB >> 25320078 |
Heinz Läubli1, Frederico Alisson-Silva2, Michal A Stanczak2, Shoib S Siddiqui2, Liwen Deng2, Andrea Verhagen2, Nissi Varki2, Ajit Varki3.
Abstract
Lectin galactoside-binding soluble 3 binding protein (LGALS3BP, also called Mac-2 binding protein) is a heavily glycosylated secreted molecule that has been shown previously to be up-regulated in many cancers and has been implicated in tumor metastatic processes, as well as in other cell adhesion and immune functions. The CD33-related subset of sialic acid-binding immunoglobulin-like lectins (Siglecs) consists of immunomodulatory molecules that have recently been associated with the modulation of immune responses to cancer. Because up-regulation of Siglec ligands in cancer tissue has been observed, the characterization of these cancer-associated ligands that bind to inhibitory CD33-related Siglecs could provide novel targets for cancer immunomodulatory therapy. Here we used affinity chromatography of tumor cell extracts to identify LGALS3BP as a novel sialic acid-dependent ligand for human Siglec-9 and for other immunomodulatory Siglecs, such as Siglec-5 and Siglec-10. In contrast, the mouse homolog Siglec-E binds to murine LGALS3BP with lower affinity. LGALS3BP has been observed to be up-regulated in human colorectal and prostate cancer specimens, particularly in the extracellular matrix. Finally, LGALS3BP was able to inhibit neutrophil activation in a sialic acid- and Siglec-dependent manner. These findings suggest a novel immunoinhibitory function for LGALS3BP that might be important for immune evasion of tumor cells during cancer progression.Entities:
Keywords: Cancer; Galectin; Glycobiology; LGALS3BP; Sialic Acid; Siglecs; Tumor Immunology
Mesh:
Substances:
Year: 2014 PMID: 25320078 PMCID: PMC4246102 DOI: 10.1074/jbc.M114.593129
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157