Evidence map›Paper›PMID 24591635›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Mapping posttranscriptional regulation of the human glycome uncovers microRNA defining the glycocode.

Praveen Agrawal, Tomasz Kurcon, Kanoelani T Pilobello, John F Rakus, Sujeethraj Koppolu, Zhongyin Liu, Bianca S Batista, William S Eng, Ku-Lung Hsu, Yaxuan Liang and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 79 citations in OpenAlex.

  1. Review
  2. Article
  3. The Critical Role of GALNTs-Regulated O-GalNAc Glycosylation in Cancer Malignancy.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
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  11. Article
  12. Article
  13. Article
  14. Review
  15. GANAB andInternational journal of molecular sciences · 2022
    Review
  16. Article
  17. Heritability of the glycan clock of biological age.Frontiers in cell and developmental biology · 2022
    Article
  18. Article
  19. Review
  20. Glycoengineering of Mammalian Expression Systems on a Cellular Level.Advances in biochemical engineering/biotechnology · 2021
    Article
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

11 authors at 3 institutions in 2 countries.

Praveen AgrawalBiomedical Chemistry Institute, Department of Chemistry, New York University, New York, NY 10003.
Tomasz Kurcon
Kanoelani T Pilobello
John F Rakus
Sujeethraj Koppolu
Zhongyin Liu
Bianca S Batista
William S Eng
Ku-Lung Hsu
Yaxuan Liang
Lara K Mahal
New York University · USInstitut de Biologie Moléculaire et Cellulaire · FRThe University of Texas at Austin · US

Funding

An integrated systems approach to deconstructing glycosylationDP2OD004711 · OD · UNIVERSITY OF TEXAS AT AUSTIN · PI MAHAL, LARA K. · 2008 to 2008
$1.8M
NIH HHS 7 DP2 OD004711-02NIH HHS DP2 OD004711
6 · The paper itself

Abstract

Cell surface glycans form a critical interface with the biological milieu, informing diverse processes from the inflammatory cascade to cellular migration. Assembly of discrete carbohydrate structures requires the coordinated activity of a repertoire of proteins, including glycosyltransferases and glycosidases. Little is known about the regulatory networks controlling this complex biosynthetic process. Recent work points to a role for microRNA (miRNA) in the regulation of specific glycan biosynthetic enzymes. Herein we take a unique systems-based approach to identify connections between miRNA and the glycome. By using our glycomic analysis platform, lectin microarrays, we identify glycosylation signatures in the NCI-60 cell panel that point to the glycome as a direct output of genomic information flow. Integrating our glycomic dataset with miRNA data, we map miRNA regulators onto genes in glycan biosynthetic pathways (glycogenes) that generate the observed glycan structures. We validate three of these predicted miRNA/glycogene regulatory networks: high mannose, fucose, and terminal β-GalNAc, identifying miRNA regulation that would not have been observed by traditional bioinformatic methods. Overall, our work reveals critical nodes in the global glycosylation network accessible to miRNA regulation, providing a bridge between miRNA-mediated control of cell phenotype and the glycome.

Indexed as

Biosynthetic PathwaysBlotting, WesternCell LineGene Expression Regulation, EnzymologicGene Regulatory NetworksGlycomicsGlycosylationHumansLuciferasesMicroarray AnalysisMicroRNAsMicroscopy, FluorescencePolysaccharidesReal-Time Polymerase Chain ReactionSystems BiologyLuciferasesMicroRNAsPolysaccharidescarbohydrate biosynthesisepigeneticsglycan regulationNCI-60systems biology

Identifiers

PMID24591635
PMCPMC3964104
OpenAlexW2152837700

What OpenQuestion holds

Textmetadata
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.