Sort   by:  
 Page size 
ProteomicsIdentification of downstream proteins of B3GNT5
Pancreatic cancer (PC) is one of the most lethal solid malignancies and new therapeutic strategies are urgently needed. β1,3-N-acetylglucosaminyltransferase V (B3GNT5) may be a potential option for cancer treatment, but its role in pancreatic cancer remains unknown. We systematically verified the re...
ORGANISM(S): Homo sapiens (Human) 
2025-05-07 | PXD052421 | Pride
Human Lc-ms label-free quantitative proteomics 
UnknownElevated transcription and glycosylation of B3GNT5 promotes breast cancer aggressiveness.
Not available
S-EPMC9077843 | biostudies-literature
UnknownRegulation of EMT-MET and chemoresistance by the Lc3Cer-synthase B3GNT5.
Not available
S-EPMC12372232 | biostudies-literature
UnknownB3GNT5 is a novel marker correlated with malignant phenotype and poor outcome in pancreatic cancer.
Not available
S-EPMC11421285 | biostudies-literature
UnknownPan-cancer analysis of B3GNT5 with potential implications for cancer immunotherapy and cancer stem cell stemness.
Not available
S-EPMC11642946 | biostudies-literature
UnknownB3GNT5 is a novel marker correlated with stem-like phenotype and poor clinical outcome in human gliomas.
Not available
S-EPMC7564194 | biostudies-literature
UnknownlncRNA MIR4435‑2HG promotes the progression of liver cancer by upregulating B3GNT5 expression.
Not available
S-EPMC8669657 | biostudies-literature
ProteomicsTumor-expressed SPPL3 supports innate anti-tumor immune responses
The development of an effective anti-tumor response relies on the synergistic actions of various immune cells that recognize tumor cells via distinct receptors. Tumors, however, often manipulate receptor-ligand interactions to evade recognition by the immune system. Recently, we highlighted the role...
ORGANISM(S): Homo sapiens (Human) 
2025-09-30 | PXD056501 | Pride
Sppl3 Cd8 t-cells Anti-tumor response B3gnt5 
OtherFucosylated glycoproteins and fucosylated glycolipids play opposing roles in cholera intoxication
Cholera toxin (CT) is the etiological agent of cholera. Here we report that multiple classes of fucosylated glycoconjugates function in CT binding and intoxication of intestinal epithelial cells. In Colo205 cells, knockout of B3GNT5, the enzyme required for synthesis of lacto- and neolacto-series gl...
ORGANISM(S): Homo sapiens 
2024-08-31 | GSE242156 | GEO
UnknownLack of lacto/neolacto-glycolipids enhances the formation of glycolipid-enriched microdomains, facilitating B cell activation.
Not available
S-EPMC2900644 | biostudies-literature
Sort   by:  
 Page size