Evidence map›Paper›PMID 29146736›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2018

Quantitative high-throughput screening identifies cytoprotective molecules that enhance SUMO conjugation via the inhibition of SUMO-specific protease (SENP)2.

Joshua D Bernstock, Daniel Ye, Jayden A Smith, Yang-Ja Lee, Florian A Gessler, Adam Yasgar, Jennifer Kouznetsova, Ajit Jadhav, Zhuoran Wang, Stefano Pluchino and 4 more

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. SUMOtherapeutics for Ischemic Stroke.Pharmaceuticals (Basel, Switzerland) · 2023
    Review
  5. Review
  6. Review
  7. Review
  8. Article
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  11. Review
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  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. SUMOylation in Glioblastoma: A Novel Therapeutic Target.International journal of molecular sciences · 2019
    Review
  20. 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

14 authors at 9 institutions in 2 countries.

Joshua D BernstockStroke Branch, National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health, Bethesda, Maryland, USA.
Daniel YeStroke Branch, National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health, Bethesda, Maryland, USA.
Jayden A SmithDivision of Stem Cell Neurobiology, Department of Clinical Neurosciences, Wellcome Trust-Medical Research Council Stem Cell Institute and National Institute of Health Research Biomedical Research Centre, University of Cambridge, United Kingdom.
Yang-Ja LeeStroke Branch, National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health, Bethesda, Maryland, USA.
Florian A GesslerDivision of Stem Cell Neurobiology, Department of Clinical Neurosciences, Wellcome Trust-Medical Research Council Stem Cell Institute and National Institute of Health Research Biomedical Research Centre, University of Cambridge, United Kingdom.
Adam YasgarNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, USA; and.
Jennifer KouznetsovaNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, USA; and.
Ajit JadhavNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, USA; and.
Zhuoran WangCenter for Perioperative Organ Protection, Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina, USA.
Stefano PluchinoDivision of Stem Cell Neurobiology, Department of Clinical Neurosciences, Wellcome Trust-Medical Research Council Stem Cell Institute and National Institute of Health Research Biomedical Research Centre, University of Cambridge, United Kingdom.
Wei ZhengNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, USA; and.
Anton SimeonovNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, USA; and.
John M HallenbeckStroke Branch, National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health, Bethesda, Maryland, USA.
Wei YangCenter for Perioperative Organ Protection, Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina, USA.
National Center for Advancing Translational Sciences · USNational Institutes of Health · USNational Institute of Neurological Disorders and Stroke · USDuke Medical Center · USDuke University Hospital · USMedical Research Council · GBNIHR Biomedical Research Centre at The Royal Marsden and the ICRUniversity of Alabama at Birmingham · USWellcome/MRC Cambridge Stem Cell Institute · GB

Funding

Drug Repurposing Screening for Rare and Neglected DiseasesZIATR000018 · NCATS · NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES · PI ZHENG, WEI · 2015 to 2025
$24.6M
Protective Mechanisms In Cerebral IschemiaZIANS002924 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI HALLENBECK, JOHN · 2009 to 2018
$16.5M
Hibernation--a New Approach To Stroke TherapyZIANS002856 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI HALLENBECK, JOHN · 2009 to 2018
$9.9M
The Unfolded Protein Response in Ischemic StrokeR01NS099590 · NINDS · DUKE UNIVERSITY · PI Wei Yang · 2016 to 2026
$3.7M
Medical Research Council MC_PC_12009NINDS NIH HHS R01 NS099590
6 · The paper itself

Abstract

The development of novel neuroprotective treatments for acute stroke has been fraught with failures, which supports the view of ischemic brain damage as a highly complex multifactorial process. Post-translational modifications such as small ubiquitin-like modifier (SUMO)ylation have emerged as critical molecular regulatory mechanisms in states of both homeostasis and ischemic stress, as evidenced by our previous work. Accordingly, the clinical significance of the selective control of the global SUMOylation process has become apparent in studies of ischemic pathobiology and pathophysiology. Herein, we describe a process capable of identifying and characterizing small molecules with the potential of targeting the SUMO system through inhibition of SUMO deconjugation in an effort to develop novel stroke therapies.-Bernstock, J. D., Ye, D., Smith, J. A., Lee, Y.-J., Gessler, F. A., Yasgar, A., Kouznetsova, J., Jadhav, A., Wang, Z., Pluchino, S., Zheng, W., Simeonov, A., Hallenbeck, J. M., Yang, W. Quantitative high-throughput screening identifies cytoprotective molecules that enhance SUMO-conjugation via the inhibition of SUMO-specific protease (SENP)2.

Indexed as

SumoylationAdaptor Proteins, Signal TransducingAnimalsCell Line, TransformedCysteine EndopeptidasesHumansProtease InhibitorsRatsStrokeSUMO-1 ProteinAdaptor Proteins, Signal TransducingCysteine EndopeptidasesProtease InhibitorsSENP2 protein, humanSenp2 protein, ratSUMO-1 Proteindrug repurposingischemianeuroprotectionstrokeSUMOylation

Identifiers

PMID29146736
PMCPMC5892725
OpenAlexW2770646696

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.