Also, although the present study does not directly examine the functional role of oligomannoses in bladder cancer, prior research demonstrates that these structures can be recognized by innate immune receptors such as mannose-binding lectins (e.g., DC-SIGN and the macrophage mannose receptor) [57,58,59], raising the possibility that oligomannosylation modulates tumor–immune interactions, either enhancing immunosurveillance or promoting immune evasion, depending on the context. This evidence concerns the gene CD209 and urinary bladder cancer.