Target intelligence / Profile preview

UDP-GlcNAc:beta-Gal beta-1,3-N-acetylglucosaminyltransferase 5 (B3GNT5)

Target
B3GNT5
Molecular classification
Enzyme, Glycosyltransferase, Glycosphingolipid biosynthetic enzyme
01

Overview

UDP-GlcNAc:beta-Gal beta-1,3-N-acetylglucosaminyltransferase 5 (B3GNT5) is a glycosyltransferase enzyme that catalyzes the addition of N-acetylglucosamine (GlcNAc) from UDP-GlcNAc to galactose on lactosylceramide, forming lactotriaosylceramide—the precursor for the lacto- and neolacto-series glycosphingolipids[1][2][3][4][5]. These glycolipids are integral to cell membrane structure, serve as mediators of cell adhesion, signaling, and differentiation, and are critical during embryonic development. B3GNT5's dysregulation—especially its upregulation—has been implicated in several cancers, where it supports cancer stemness and correlates with poor prognosis, making it a promising but challenging therapeutic target. Knockout studies reveal its indispensability for early development and membrane microdomain structure, while its expression influences immune cell function and tumor microenvironment interactions.

Other names
Beta-1,3-N-acetylglucosaminyltransferase 5Beta-1,3-Gn-T5Beta3Gn-T5B3gnt5Lactotriaosylceramide synthaseLactosylceramide synthaseLc3 synthaseBGnT-5UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5Lactosylceramide 1,3-N-acetyl-beta-D-glucosaminyltransferase
02

Mechanism of action

siRNA-mediated knockdown (reduces stemness and neurosphere formation in glioma stem cells); Hypothetical small-molecule inhibition (would block glycosphingolipid biosynthesis, potentially preventing malignant or stem-like cell properties); Indirect modulation via glycosylation pathways (possible effects on cellular adhesion, immune signaling, stemness)

03

Biological functions

Biosynthesis of glycosphingolipids (GSLs)—formation of lacto- and neolacto-series GSL precursorsCell adhesionCell signalingCell differentiationRegulation of membrane microdomainsEmbryonic developmentImmune response modulation
04

Disease associations

CancerEmbryonic lethality
05

Safety considerations

Essential for embryonic developmentPotential widespread physiological disruptionPossible impact on immune function
06

Interacting drugs

No approved direct drugs targeting B3GNT5 are currently described in the literature.
07

Biomarkers

B3GNT5 expression levelLacto-/neolacto-series glycosphingolipid levels

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