“…In this context, several clinical studies have unveiled glycan-associated signatures (glycans, glycan binding proteins, glycosyltranserases, heavily glycosylated proteins/lipids/GPI-anchored molecules) associated with more aggressive cancer cell phenotypes, tumour recurrence, progression, metastization, or decreased overall survival. Particularly, in bladder cancer, the presence/overexpression of GnT-III/IV, Le x , Le y , SLe x , STn, ST6GalNAc.I, T-antigen, ST3Gal.I, HER2, EpCAM, galectin-1, galectin-3, CD44, CD44v9, MUC1, MUC4, ITGA6, ITGAV, neuropilin-1, neuropilin-2, versican, decorin, biglycan, endocan, HYAL1, hyaluronic acid synthase 1, RHAAM, glucosylceramide synthase, and PIG-U was associated with more aggressive phenotypes and/or poor prognosis [ 20 , 30 , 46 , 50 , 54 , 64 - 67 , 76 , 82 , 86 , 87 , 96 , 97 , 101 - 103 , 120 , 121 , 124 , 125 , 129 , 133 , 139 , 165 - 168 , 171 , 172 , 176 , 177 , 179 - 181 , 198 , 208 , 209 ]. By another hand, (over)expression of β-1-6GalNAc antennae, galectin-7, CD44v6, MUC2, MUC6, glycolipid enzyme GM3, and CD109 were linked to a less aggressive phenotype and/or better prognosis [ 32 , 104 , 121 , 122 , 129 , 199 , 213 ].…”