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Multifunctionalized Brush-Like Glycopolymers with High Affinity to P-Selectin and Antitumor Metastasis Activity
- Source :
- Biomacromolecules. 22:1177-1185
- Publication Year :
- 2021
- Publisher :
- American Chemical Society (ACS), 2021.
-
Abstract
- Glycopolymers that can mimic natural glycosaminoglycan, such as heparin, have shown great potentials in inhibition of cancer metastasis. In the current work, a novel series of brush-like glycopolymers (BGPs) with simultaneous functionalization of various monosaccharide or disaccharide compositions have been synthesized through a new grafting-polymerization strategy, in order to mimic the activities of both heparin and P-selectin ligand PSGL-1. In the subsequent in vitro assays of antiadhesion, platelets activation, heparanase inhibition, and so on, BGP-SFH, as one of the BGPs with the composition of the combined three sugar units, sialic acids, fucoses, and heparin disaccharides, showed the highest antimetastasis ability, similar to its prototype heparin. Moreover, in a mouse metastatic melanoma model, the BGP-SFH also inhibited B16 cell metastasis effectively. Thus, the current work not only demonstrated a type of promising antimetastasis glycopolymer BGPs, but also illustrated an easy synthetic approach to multifunctionalized glycopolymers, leading to potential applications for broader biomedical research.
- Subjects :
- Polymers and Plastics
Glycopolymer
Cell
Disaccharide
Bioengineering
02 engineering and technology
010402 general chemistry
01 natural sciences
Polymerization
Biomaterials
Glycosaminoglycan
Mice
chemistry.chemical_compound
Neoplasms
Materials Chemistry
medicine
Animals
Monosaccharide
Heparanase
Neoplasm Metastasis
chemistry.chemical_classification
Heparin
021001 nanoscience & nanotechnology
Ligand (biochemistry)
0104 chemical sciences
P-Selectin
medicine.anatomical_structure
chemistry
Biochemistry
0210 nano-technology
medicine.drug
Subjects
Details
- ISSN :
- 15264602 and 15257797
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- Biomacromolecules
- Accession number :
- edsair.doi.dedup.....192338b9b9962259b75cfc77efc96c01