Evidence map›Paper›PMID 26807114›Full record

ArticleNeural regeneration research2015

MicroRNAs: a novel promising therapeutic target for cerebral ischemia/reperfusion injury?

Xiao-Li Min, Ting-Yong Wang, Yi Cao, Jia Liu, Jin-Tao Li, Ting-Hua Wang

Abstract read
In one paragraph

Article in Neural regeneration research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

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  16. Inhibition ofBioscience reports · 2017
    Article
  17. [Yiqihuoxue prescription promotes nerve regeneration by miR-124-mediated regulation of Wnt signaling in rats].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2017
    Article
  18. Article
  19. Pigmy MicroRNA: surveillance cops in Therapies kingdom.Molecular medicine (Cambridge, Mass.) · 2016
    Article
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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.

Xiao-Li MinInstitute of Neuroscience, Kunming Medical University, Kunming, Yunnan Province, China; Faculty of Clinical Medicine, Yunnan University of Traditional Chinese Medicine; the First Affiliated Hospital of Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan Province, China.
Ting-Yong WangSchool of Economics of Sichuan University, Chengdu, Sichuan Province, China.
Yi CaoDepartment of Neurosurgery, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan Province, China.
Jia LiuInstitute of Neuroscience, Kunming Medical University, Kunming, Yunnan Province, China.
Jin-Tao LiInstitute of Neuroscience, Kunming Medical University, Kunming, Yunnan Province, China.
Ting-Hua WangInstitute of Neuroscience, Kunming Medical University, Kunming, Yunnan Province, China.ORCID 0000-0002-5353-4810

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To determine the molecular mechanism of cerebral ischemia/reperfusion injury, we examined the microRNA (miRNA) expression profile in rat cortex after focal cerebral ischemia/reperfusion injury using miRNA microarrays and bioinformatic tools to systematically analyze Gene Ontology (GO) function classifications, as well as the signaling pathways of genes targeted by these differentially expressed miRNAs. Our results show significantly changed miRNA expression profiles in the reperfusion period after focal cerebral ischemia, with a total of 15 miRNAs up-regulated and 44 miRNAs down-regulated. Target genes of these differentially expressed miRNAs were mainly involved in metabolic and cellular processes, which were identified as hub nodes of a miRNA-GO-network. The most correlated pathways included D-glutamine and D-glutamate metabolism, the renin-angiotensin system, peroxisomes, the PPAR signaling pathway, SNARE interactions in vesicular transport, and the calcium signaling pathway. Our study suggests that miRNAs play an important role in the pathological process of cerebral ischemia/reperfusion injury. Understanding miRNA expression and function may shed light on the molecular mechanism of cerebral ischemia/reperfusion injury.

Indexed as

bioinformatics analysiscerebral ischemia/reperfusion injuryGene Ontology analysisKEGG pathwaymicroRNAmiRNA expression profilesmolecular mechanismnerve regenerationneural regenerationtherapeutic target

Identifiers

PMID26807114
PMCPMC4705791

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Registered trials

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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.