Evidence map›Paper›PMID 30344053›Full record

ArticleCell chemical biology2018

Thioglycosides Are Efficient Metabolic Decoys of Glycosylation that Reduce Selectin Dependent Leukocyte Adhesion.

Shuen-Shiuan Wang, Xuefeng Gao, Virginia Del Solar, Xinheng Yu, Aristotelis Antonopoulos, Alan E Friedman, Eryn K Matich, G Ekin Atilla-Gokcumen, Mehrab Nasirikenari, Joseph T Lau and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell chemical biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 36 citations in OpenAlex.

  1. Synthetic Ligands of Myeloid C-Type Lectin Receptors.Chembiochem : a European journal of chemical biology · 2026
    Review
  2. AssessingACS infectious diseases · 2026
    Article
  3. Article
  4. Thioglycoside functionalizationChemical communications (Cambridge, England) · 2025
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Comparative Glycomics Analysis of Mass Spectrometry Data.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 2 countries.

Shuen-Shiuan WangDepartment of Chemical and Biological Engineering, State University of New York, 906 Furnas Hall, Buffalo, NY 14260, USA.
Xuefeng GaoTumorEnd LLC, Louisiana Emerging Technology Center, 340 East Parker Drive, Suite 246, Baton Rouge, LA 70803, USA.
Virginia Del SolarDepartment of Chemical and Biological Engineering, State University of New York, 906 Furnas Hall, Buffalo, NY 14260, USA; Clinical & Translational Research Center and State University of New York, Buffalo, NY 14260, USA.
Xinheng YuDepartment of Chemical and Biological Engineering, State University of New York, 906 Furnas Hall, Buffalo, NY 14260, USA.
Aristotelis AntonopoulosDepartment of Life Sciences, Imperial College London, London SW7 2AZ, UK.
Alan E FriedmanDepartment of Chemistry, State University of New York, Buffalo, NY 14260, USA.
Eryn K MatichDepartment of Chemistry, State University of New York, Buffalo, NY 14260, USA.
G Ekin Atilla-GokcumenDepartment of Chemistry, State University of New York, Buffalo, NY 14260, USA.
Mehrab NasirikenariDepartment of Cellular and Molecular Biology, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
Joseph T LauDepartment of Cellular and Molecular Biology, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
Anne DellDepartment of Life Sciences, Imperial College London, London SW7 2AZ, UK.
Stuart M HaslamDepartment of Life Sciences, Imperial College London, London SW7 2AZ, UK.
Roger A LaineTumorEnd LLC, Louisiana Emerging Technology Center, 340 East Parker Drive, Suite 246, Baton Rouge, LA 70803, USA.
Khushi L MattaDepartment of Chemical and Biological Engineering, State University of New York, 906 Furnas Hall, Buffalo, NY 14260, USA; TumorEnd LLC, Louisiana Emerging Technology Center, 340 East Parker Drive, Suite 246, Baton Rouge, LA 70803, USA. Electronic address: klmatta40@gmail.com.
Sriram NeelameghamDepartment of Chemical and Biological Engineering, State University of New York, 906 Furnas Hall, Buffalo, NY 14260, USA; Clinical & Translational Research Center and State University of New York, Buffalo, NY 14260, USA. Electronic address: neel@buffalo.edu.
University at Buffalo, State University of New York · USImperial College London · GBTumorEnd (United States) · USRoswell Park Comprehensive Cancer Center · US

Funding

REGULATION OF LACTOSAMINYL GLYCAN BIOSYNTHESIS IN HEMATOPOIETIC CELLSP01HL107146 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SACKSTEIN, ROBERT · 2011 to 2017
$17.7M
Systems Biology of GlycosylationR01HL103411 · NHLBI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI NEELAMEGHAM, SRIRAM · 2011 to 2025
$7.1M
Synthetic glycan biomarkers: Novel reporters of cell metabolismR21GM126537 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI NEELAMEGHAM, SRIRAM · 2018 to 2019
$439k
Small Cell-Penetrating Glyco-Decoys Sidetrack Selectin Ligand BiosynthesisR43GM106513 · NIGMS · TUMOREND, LLC · PI MATTA, KHUSHI L · 2013 to 2013
$149k
Biotechnology and Biological Sciences Research Council BB/K016164/1NHLBI NIH HHS P01 HL107146NHLBI NIH HHS R01 HL103411NIGMS NIH HHS R21 GM126537NIGMS NIH HHS R43 GM106513
6 · The paper itself

Abstract

Metabolic decoys are synthetic analogs of naturally occurring biosynthetic acceptors. These compounds divert cellular biosynthetic pathways by acting as artificial substrates that usurp the activity of natural enzymes. While O-linked glycosides are common, they are only partially effective even at millimolar concentrations. In contrast, we report that N-acetylglucosamine (GlcNAc) incorporated into various thioglycosides robustly truncate cell surface N- and O-linked glycan biosynthesis at 10-100 μM concentrations. The >10-fold greater inhibition is in part due to the resistance of thioglycosides to hydrolysis by intracellular hexosaminidases. The thioglycosides reduce β-galactose incorporation into lactosamine chains, cell surface sialyl Lewis-X expression, and leukocyte rolling on selectin substrates including inflamed endothelial cells under fluid shear. Treatment of granulocytes with thioglycosides prior to infusion into mouse inhibited neutrophil homing to sites of acute inflammation and bone marrow by ∼80%-90%. Overall, thioglycosides represent an easy to synthesize class of efficient metabolic inhibitors or decoys. They reduce N-/O-linked glycan biosynthesis and inflammatory leukocyte accumulation.

Indexed as

AnimalsCell AdhesionGlycosylationHL-60 CellsHumansInflammationLeukocytesMiceMice, Inbred C57BLMolecular StructureSmall Molecule LibrariesThioglycosidesSmall Molecule LibrariesThioglycosidesdecoyfluid shearglycosidesglycosylationinflammationleukocyte-endothelial adhesionN-glycanselectinssmall-molecule inhibitorsthioglycoside

Identifiers

PMID30344053
PMCPMC6474417
OpenAlexW2896106474

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.