Target intelligence / Profile preview

Galactose-3-O-sulfotransferase 2 (GAL3ST2)

Target
GAL3ST2
Molecular classification
Enzyme, Sulfotransferase
01

Overview

Galactose-3-O-sulfotransferase 2 (GAL3ST2) is an enzyme of the galactose-3-O-sulfotransferase family that catalyzes the transfer of sulfate to the C-3 hydroxyl group of non-reducing beta-galactosyl residues in diverse glycoconjugates[1][3]. This modification predominantly occurs on both type 1 and type 2 oligosaccharides and on core 1 mucin-type O-glycans, facilitating the biosynthesis of 3′-sulfated glycan structures such as 3′-sulfo-Lewis antigens[1][2]. GAL3ST2 expression is found in multiple tissues, notably in the gastrointestinal tract mucosa, and it is involved in the synthesis of sulfomucins that are important for mucosal barrier integrity[4]. Dysregulation or altered expression of GAL3ST2 has been associated with tumor metastasis and certain cancers, with increased sulfation of tumor cell surface glycans impacting cell–cell interactions and possibly immune recognition[1][5]. No drugs are currently approved that directly target this enzyme, but it is considered a promising molecular enzyme target for altering glycosylation-dependent cell processes in oncology and mucosal biology[1][3][5].

Other names
GP3STGal3ST-2Beta-galactose-3-O-sulfotransferase 2Gal-beta-1,3-GalNAc 3'-sulfotransferase 2Glycoprotein beta-Gal 3'-sulfotransferase 2gal 3-O-sulphotransferasegal-beta-1,3-GalNAc 3'-sulfotransferase 2galbeta1-3GalNAc 3'-sulfotransferase 2GAL3ST-2
02

Mechanism of action

no drugs with characterized mechanism of action targeting GAL3ST2; the enzyme’s modification of glycan structures could, in principle, alter cell recognition or binding by certain therapeutic agents or antibodies[5]

03

Biological functions

Sulfation of beta-galactosyl residuesGlycosylation of proteins and lipidsModification of mucin O-glycansInvolvement in synthesis of sulfomucinsSynthesis of 3'-sulfated Lewis antigens
04

Disease associations

Cancer (e.g., roles in tumor metastasis)Other (implicated in modulating glycan structures relevant for tumor progression and mucosal barrier function)
05

Safety considerations

Potential on-target effects on normal glycan sulfation in healthy tissues, especially within the gastrointestinal tract and mucosal barriers (speculated, based on biological function[4])Modulation of glycosylation pathways may alter immune recognition or mucosal protection (hypothetical, as direct inhibitors have not been clinically developed)
06

Biomarkers

Expression of 3′-sulfo-TF (Thomsen–Friedenreich) antigen as a marker for certain cancers[5]GAL3ST2 mRNA/protein levels may serve as a biomarker in tumor tissues (correlated with metastatic potential and response to some experimental agents[5])

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