Evidence map›Paper›PMID 29114076›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2018

Circular RNA DLGAP4 Ameliorates Ischemic Stroke Outcomes by Targeting miR-143 to Regulate Endothelial-Mesenchymal Transition Associated with Blood-Brain Barrier Integrity.

Ying Bai, Yuan Zhang, Bing Han, Li Yang, Xufeng Chen, Rongrong Huang, Fangfang Wu, Jie Chao, Pei Liu, Gang Hu and 2 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 234 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
234citing papers in PubMed, 3 pooled it
14.9field-weighted citation impact, top 1% 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

234 citing papers in PubMed, 3 syntheses or guidelines pooled it, 379 citations in OpenAlex.

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  19. CD8Cellular & molecular immunology · 2025
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174 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Ying BaiDepartment of Pharmacology, School of Medicine, Southeast University, Nanjing 210009, China.
Yuan ZhangDepartment of Pharmacology, School of Medicine, Southeast University, Nanjing 210009, China.
Bing HanDepartment of Pharmacology, School of Medicine, Southeast University, Nanjing 210009, China.
Li YangDepartment of Pharmacology, School of Medicine, Southeast University, Nanjing 210009, China.
Xufeng ChenEmergency Department, Jiangsu Province Hospital, Nanjing 210029, China.
Rongrong HuangDepartment of Pharmacology, School of Medicine, Southeast University, Nanjing 210009, China.
Fangfang WuDepartment of Pharmacology, School of Medicine, Southeast University, Nanjing 210009, China.
Jie ChaoDepartment of Physiology, School of Medicine, Southeast University, Nanjing 210009, China.
Pei LiuDepartment of Epidemiology and Biostatistics, School of Public Health, Southeast University, Nanjing 210009, China.
Gang HuJiangsu Key Laboratory of Neurodegeneration, Department of Pharmacology, Nanjing Medical University, Nanjing 210029, China.
John H ZhangDepartment of Anesthesiology, School of Medicine, Loma Linda University, Loma Linda, California 92354, and.
Honghong YaoDepartment of Pharmacology, School of Medicine, Southeast University, Nanjing 210009, China, yaohh@seu.edu.cn.
Southeast University · CNJiangsu Province Hospital · CNLoma Linda University · USNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circular RNAs (circRNAs) are highly expressed in the CNS and regulate physiological and pathophysiological processes. However, the potential role of circRNAs in stroke remains largely unknown. Here, we show that the circRNA DLGAP4 (circDLGAP4) functions as an endogenous microRNA-143 (miR-143) sponge to inhibit miR-143 activity, resulting in the inhibition of homologous to the E6-AP C-terminal domain E3 ubiquitin protein ligase 1 expression. circDLGAP4 levels were significantly decreased in the plasma of acute ischemic stroke patients (13 females and 13 males) and in a mouse stroke model. Upregulation of circDLGAP4 expression significantly attenuated neurological deficits and decreased infarct areas and blood-brain barrier damage in the transient middle cerebral artery occlusion mouse stroke model. Endothelial-mesenchymal transition contributes to blood-brain barrier disruption and circDLGAP4 overexpression significantly inhibited endothelial-mesenchymal transition by regulating tight junction protein and mesenchymal cell marker expression. Together, the results of our study are illustrative of the involvement of circDLGAP4 and its coupling mechanism in cerebral ischemia, providing translational evidence that circDLGAP4 serves as a novel therapeutic target for acute cerebrovascular protection.

Indexed as

AnimalsBlood-Brain BarrierBrain IschemiaCerebrovascular CirculationDisks Large Homolog 4 ProteinEpithelial-Mesenchymal TransitionGene SilencingHumansInfarction, Middle Cerebral ArteryMagnetic Resonance ImagingMaleMiceMice, Inbred C57BLMicroRNAsRNARNA, CircularDisks Large Homolog 4 ProteinDlg4 protein, mouseHectd1 protein, mouseMicroRNAsMIRN143 microRNA, mouseRNARNA, CircularTight Junction ProteinsUbiquitin-Protein Ligasesblood–brain barrier integritycircular RNA DLGAP4endothelial-mesenchymal transitionischemic strokemiR-143transient middle cerebral artery occlusion

Identifiers

PMID29114076
PMCPMC6705810
OpenAlexW2767779948

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.