Evidence map›Paper›PMID 29574014›Full record

ReviewProgress in neurobiology

Notch signaling and neuronal death in stroke.

Thiruma V Arumugam, Sang-Ha Baik, Priyanka Balaganapathy, Christopher G Sobey, Mark P Mattson, Dong-Gyu Jo

Open access · greenAbstract readReview
In one paragraph

Review in Progress in neurobiology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

75 citing papers in PubMed, 140 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Innovative approaches for the treatment of stroke: a recent update.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Biomedicines · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

15 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 4 countries.

Thiruma V ArumugamDepartment of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; School of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea. Electronic address: phstva@nus.edu.sg.
Sang-Ha BaikDepartment of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Priyanka BalaganapathyDepartment of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Christopher G SobeyDepartment of Physiology, Anatomy & Microbiology, School of Life Sciences, La Trobe University, Melbourne, Victoria, Australia.
Mark P MattsonLaboratory of Neurosciences, National Institute on Aging Intramural Research Program, Baltimore, MD, USA; Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Dong-Gyu JoSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea. Electronic address: jodg@skku.edu.
National University of Singapore · SGSungkyunkwan University · KRLa Trobe University · AUNational Institute on Aging · US

Funding

Intramural NIH HHS Z99 AG999999
6 · The paper itself

Abstract

Ischemic stroke is a leading cause of morbidity and death, with the outcome largely determined by the amount of hypoxia-related neuronal death in the affected brain regions. Cerebral ischemia and hypoxia activate the Notch1 signaling pathway and four prominent interacting pathways (NF-κB, p53, HIF-1α and Pin1) that converge on a conserved DNA-associated nuclear multi-protein complex, which controls the expression of genes that can determine the fate of neurons. When neurons experience a moderate level of ischemic insult, the nuclear multi-protein complex up-regulates adaptive stress response genes encoding proteins that promote neuronal survival, but when ischemia is more severe the nuclear multi-protein complex induces genes encoding proteins that trigger and execute a neuronal death program. We propose that the nuclear multi-protein transcriptional complex is a molecular mediator of neuronal hormesis and a target for therapeutic intervention in stroke.

Indexed as

AnimalsBrain IschemiaCell DeathHumansHypoxia, BrainNeuronsReceptors, NotchSignal TransductionStrokeReceptors, NotchHIF-1αHypoxiaIschemic strokeNeuronal cell deathNF-κBNotchp-53Pin-1

Identifiers

PMID29574014
PMCPMC6100747
OpenAlexW2791037419

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.