Evidence map›Paper›PMID 25336635›Full record

ReviewThe Journal of biological chemistry2014

Protein O-GlcNAcylation and cardiovascular (patho)physiology.

Susan A Marsh, Helen E Collins, John C Chatham

Abstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
–field-weighted citation impact
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

59 citing papers in PubMed.

  1. Review
  2. Article
  3. International journal of molecular sciences · 2025
    Review
  4. The Role of Uridine in Health and Disease.Journal of inflammation research · 2025
    Review
  5. Improving metabolic support during normothermicFrontiers in cardiovascular medicine · 2025
    Review
  6. PERM1 regulates mitochondrial energetics through O-GlcNAcylation in the heart.Journal of molecular and cellular cardiology · 2025
    Article
  7. Review
  8. Review
  9. Article
  10. The O-GlcNAc dichotomy: when does adaptation become pathological?Clinical science (London, England : 1979) · 2023
    Review
  11. Article
  12. OGT controls mammalian cell viability by regulating the proteasome/mTOR/ mitochondrial axis.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Metabolites · 2021
    Article
  18. Article
  19. Role ofPhysiological reviews · 2021
    Review
  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

3 authors.

Susan A MarshFrom the Section of Experimental and Systems Pharmacology, College of Pharmacy, Washington State University, Spokane, Washington 99210-1495 and.
Helen E Collinsthe Division of Molecular and Cellular Pathology, Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama 35294-0019.
John C Chathamthe Division of Molecular and Cellular Pathology, Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama 35294-0019 jchatham@uab.edu.

Funding

Protein O-GlcNAcylation and the regulation of cardiac functionR01HL101192 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CHATHAM, JOHN C · 2010 to 2014
$1.5M
The Western diet and O-GlcNAc modification of chromatin proteinsR15HL104549 · NHLBI · WASHINGTON STATE UNIVERSITY · PI MARSH, SUSAN ANNE · 2011 to 2011
$451k
STIM1 mediated calcium entry: A new paradigm of metabolic regulation of cardiomyoR21HL110366 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CHATHAM, JOHN C · 2012 to 2013
$407k
NHLBI NIH HHS HL-101192NHLBI NIH HHS HL-104549NHLBI NIH HHS HL-110366NHLBI NIH HHS R01 HL101192NHLBI NIH HHS R15 HL104549NHLBI NIH HHS R21 HL110366
6 · The paper itself

Abstract

Our understanding of the role of protein O-GlcNAcylation in the regulation of the cardiovascular system has increased rapidly in recent years. Studies have linked increased O-GlcNAc levels to glucose toxicity and diabetic complications; conversely, acute activation of O-GlcNAcylation has been shown to be cardioprotective. However, it is also increasingly evident that O-GlcNAc turnover plays a central role in the delicate regulation of the cardiovascular system. Therefore, the goals of this minireview are to summarize our current understanding of how changes in O-GlcNAcylation influence cardiovascular pathophysiology and to highlight the evidence that O-GlcNAc cycling is critical for normal function of the cardiovascular system.

Indexed as

AcetylglucosamineAnimalsCalcium SignalingCardiovascular SystemEpigenesis, GeneticGlycosylationHumansProteinsAcetylglucosamineProteinsCalciumCardiac HypertrophyCardiovascularEpigeneticsO-Linked N-Acetylglucosamine (O-GlcNAc)

Identifiers

PMID25336635
PMCPMC4263852

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.