Evidence map›Paper›PMID 28860495›Full record

ArticleScientific reports2017

miR-96 attenuates status epilepticus-induced brain injury by directly targeting Atg7 and Atg16L1.

Jing Gan, Qianyun Cai, Yi Qu, Fengyan Zhao, Chaomin Wan, Rong Luo, Dezhi Mu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 23% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Jing GanDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.
Qianyun CaiDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.
Yi QuDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.
Fengyan ZhaoDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.
Chaomin WanDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.
Rong LuoDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China. 1109329811@qq.com.
Dezhi MuDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China. mudz@scu.edu.cn.
Sichuan University · CNWest China Second University Hospital of Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Status epilepticus (SE) can cause brain damage and lead to neural dysfunction. Developing novel targets for SE therapy and diagnosis is important and necessary. Previously, we found several differentially expressed microRNAs (miRNAs) in the developing hippocampus following SE, including the autophagy-related miR-96. In the present study, we employed immunofluorescence staining and Western blot analysis to assess the expression of autophagy-related 7 (Atg7) and Atg16L1 and the status of autophagosome formation in the hippocampus of immature rats with SE. Additional in vivo intervention was also performed to investigate the potential therapeutic function of miR-96 in developing rats with SE. We found that Atg7 and Atg16L1 were up-regulated in the neurons after SE, together with an increase in autophagosome formation. Meanwhile, overexpression of miR-96 significantly prevented brain damage in SE rats by inhibiting Atg7 and Atg16L1 expression and autophagosome formation in the hippocampus. Furthermore, Rapamycin negated miR-96 mediated brain injury attenuation through inducing autophagosome formation. Our study indicates that miR-96 might be a potential target for therapy of pediatric SE.

Indexed as

Gene Expression RegulationRNA InterferenceAnimalsAutophagosomesAutophagyAutophagy-Related Protein 7BiomarkersBrainDisease Models, AnimalHippocampusMicroRNAsRatsStatus EpilepticusVesicular Transport ProteinsAtg16L1 protein, ratAutophagy-Related Protein 7BiomarkersMicroRNAsMIRN96 microRNA, ratVesicular Transport Proteins

Identifiers

PMID28860495
PMCPMC5579030
OpenAlexW2745909933

What OpenQuestion holds

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LicenceCC BY
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.