Evidence map›Paper›PMID 24359188›Full record

ReviewAntioxidants & redox signaling2015

The use of microRNAs to modulate redox and immune response to stroke.

Yi-Bing Ouyang, Creed M Stary, Robin E White, Rona G Giffard

Abstract readReview
In one paragraph

Review in Antioxidants & redox signaling, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.3field-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

35 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
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  3. Article
  4. Article
  5. Review
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  7. Article
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  9. Review
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  11. Review
  12. Review
  13. Article
  14. Article
  15. MicroRNAs in brain development and cerebrovascular pathophysiology.American journal of physiology. Cell physiology · 2019
    Review
  16. Exercise and Cardiovascular Progenitor Cells.Comprehensive Physiology · 2019
    Review
  17. Review
  18. MicroRNA-1906, a Novel Regulator of Toll-Like Receptor 4, Ameliorates Ischemic Injury after Experimental Stroke in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  19. 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

4 authors at 1 institution in 1 country.

Yi-Bing OuyangDepartment of Anesthesia, Stanford University School of Medicine , Stanford, California.
Creed M Stary
Robin E White
Rona G Giffard
Stanford University · US

Funding

Research in Anesthesia Training Program (ReAP)T32GM089626 · NIGMS · STANFORD UNIVERSITY · PI Vivianne L Tawfik · 2010 to 2026
$5.2M
Astrocytes and Ischemic Brain InjuryR01NS053898 · NINDS · STANFORD UNIVERSITY · PI GIFFARD, RONA G · 2007 to 2016
$3.8M
Stress Proteins in Brain Cell InjuryR01NS084396 · NINDS · STANFORD UNIVERSITY · PI GIFFARD, RONA G · 2013 to 2017
$1.7M
Mitochondrial protection in post-stroke recoveryR01NS080177 · NINDS · STANFORD UNIVERSITY · PI GIFFARD, RONA G · 2013 to 2017
$1.7M
NIGMS NIH HHS T32 GM089626NINDS NIH HHS NS053898NINDS NIH HHS NS080177NINDS NIH HHS NS084396NINDS NIH HHS R01 NS053898NINDS NIH HHS R01 NS080177NINDS NIH HHS R01 NS084396
6 · The paper itself

Abstract

significanceCerebral ischemia is a major cause of death and disability throughout the world, yet therapeutic options remain limited. The interplay between the cellular redox state and the immune response plays a critical role in determining the extent of neural cell injury after ischemia and reperfusion. Excessive amounts of reactive oxygen species (ROS) generated by mitochondria and other sources act both as triggers and effectors of inflammation. This review will focus on the interplay between these two mechanisms. RECENT ADVANCES: MicroRNAs (miRNAs) are important post-transcriptional regulators that interact with multiple target messenger RNAs coordinately regulating target genes, including those involved in controlling mitochondrial function, redox state, and inflammatory pathways. This review will focus on the regulation of mitochondria, ROS, and inflammation by miRNAs in the chain of deleterious intra- and intercellular events that lead to brain cell death after cerebral ischemia. CRITICAL ISSUES: Although pretreatment using miRNAs was effective in cerebral ischemia in rodents, testing treatment after the onset of ischemia is an essential next step in the development of acute stroke treatment. In addition, miRNA formulation and delivery into the CNS remain a challenge in the clinical translation of miRNA therapy. FUTURE DIRECTIONS: Future research should focus on post-treatment and potential clinical use of miRNAs.

Indexed as

AnimalsHumansMicroRNAsMitochondriaOxidation-ReductionReactive Oxygen SpeciesStrokeMicroRNAsReactive Oxygen Species

Identifiers

PMID24359188
PMCPMC4281877
OpenAlexW2331819647

What Socratic 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 Socratic graph.