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10.3390/ijms17091566

http://scihub22266oqcxt.onion/10.3390/ijms17091566
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C5037834!5037834 !27649167
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suck abstract from ncbi


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pmid27649167
      Int+J+Mol+Sci 2016 ; 17 (9 ): ä
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  • The Role of Galectin-1 in Cancer Progression, and Synthetic Multivalent Systems for the Study of Galectin-1 #MMPMID27649167
  • Cousin JM ; Cloninger MJ
  • Int J Mol Sci 2016[Sep]; 17 (9 ): ä PMID27649167 show ga
  • This review discusses the role of galectin-1 in the tumor microenvironment. First, the structure and function of galectin-1 are discussed. Galectin-1, a member of the galectin family of lectins, is a functionally dimeric galactoside-binding protein. Although galectin-1 has both intracellular and extracellular functions, the defining carbohydrate-binding role occurs extracellularly. In this review, the extracellular roles of galectin-1 in cancer processes are discussed. In particular, the importance of multivalent interactions in galectin-1 mediated cellular processes is reviewed. Multivalent interactions involving galectin-1 in cellular adhesion, mobility and invasion, tumor-induced angiogenesis, and apoptosis are presented. Although the mechanisms of action of galectin-1 in these processes are still not well understood, the overexpression of galectin-1 in cancer progression indicates that the role of galectin-1 is significant. To conclude this review, synthetic frameworks that have been used to modulate galectin-1 processes are reviewed. Small molecule oligomers of carbohydrates, carbohydrate-functionalized pseudopolyrotaxanes, cyclodextrins, calixarenes, and glycodendrimers are presented. These synthetic multivalent systems serve as important tools for studying galectin-1 mediated cancer cellular functions.
  • |Animals [MESH]
  • |Cell Adhesion [MESH]
  • |Cyclodextrins/chemistry/metabolism [MESH]
  • |Dendrimers/chemistry/metabolism [MESH]
  • |Extracellular Matrix/metabolism [MESH]
  • |Galectin 1/genetics/*metabolism [MESH]
  • |Humans [MESH]
  • |Neoplasm Invasiveness [MESH]
  • |Neoplasms/metabolism/*pathology [MESH]
  • |Neovascularization, Pathologic [MESH]
  • |Poloxamer/chemistry/metabolism [MESH]
  • |Rotaxanes/chemistry/metabolism [MESH]


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