4.5 Review

Current state-of-the-art on ganglioside-mediated immune modulation in the tumor microenvironment

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Summary: Endogenous sialoglycolipids and/or sialoglycoproteins bind to and initiate signaling by cell surface Siglecs, which are endogenous sialic acid-binding lectins in humans. Gangliosides play varied roles in Siglec-mediated signaling, such as ensuring stable axon-myelin interactions and inhibiting immune signaling.

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Summary: Evidence suggests that host glycans, specifically glycolipids containing sialic acid, play a role in facilitating the entry of SARS-CoV-2 virus into host cells by binding to the receptor-binding domain (RBD) of the spike protein. Depletion of cell surface sialic acid levels through various methods decreases RBD binding and infection of the virus, indicating the importance of sialylated glycans in viral entry.

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Anti-GD2 synergizes with CD47 blockade to mediate tumor eradication

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Summary: The combination of anti-GD2 and CD47 blockade demonstrates robust anti-tumor activity in mouse models, particularly effective against neuroblastoma, osteosarcoma, and small-cell lung cancer.

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Role of GD3 Synthase ST8Sia I in Cancers

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Identification of ST3GAL5 as a prognostic biomarker correlating with CD8+ T cell exhaustion in clear cell renal cell carcinoma

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Summary: Mutations in TSC lead to tumors with biallelic mutations in TSC7 or TSC2 and hyperactive mTORC1. Overexpression of GD3 was observed in affected tissues from TSC patients and aging Tsc2(+/-) mice. Treatment with GD3 CAR-T cells significantly reduced tumor burden in mice and resulted in tumor-free outcome for the majority of treated animals.

JCI INSIGHT (2021)

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Monosialic ganglioside GM3 specifically suppresses the monocyte adhesion to endothelial cells for inflammation

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Ganglioside GM3 inhibits hepatoma cell motility via down-regulating activity of EGFR and PI3K/AKT signaling pathway

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