Evidence map›Paper›PMID 25448187›Full record

ArticleSpinal cord2015

MiR-200c regulates ROS-induced apoptosis in murine BV-2 cells by targeting FAP-1.

D S Yu, G Lv, X F Mei, Y Cao, Y F Wang, Y S Wang, Y L Bi

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Spinal cord, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  10. RNA control in pain: Blame it on the messenger.Wiley interdisciplinary reviews. RNA · 2019
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  14. MicroRNA-23b attenuates the HInternational journal of clinical and experimental pathology · 2018
    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

7 authors at 2 institutions in 1 country.

D S YuDepartment of Orthopaedics, The First Affiliated Hospital, Liaoning Medical University, Jinzhou, People's Republic of China.
G LvDepartment of Orthopaedics, The First Affiliated Hospital, Liaoning Medical University, Jinzhou, People's Republic of China.
X F MeiDepartment of Orthopaedics, The First Affiliated Hospital, Liaoning Medical University, Jinzhou, People's Republic of China.
Y CaoDepartment of Orthopaedics, The First Affiliated Hospital, Liaoning Medical University, Jinzhou, People's Republic of China.
Y F WangDepartment of Orthopaedics, The First Affiliated Hospital, China Medical University, Shenyang, People's Republic of China.
Y S WangDepartment of Orthopaedics, The First Affiliated Hospital, Liaoning Medical University, Jinzhou, People's Republic of China.
Y L BiDepartment of Orthopaedics, The First Affiliated Hospital, Liaoning Medical University, Jinzhou, People's Republic of China.
Jinzhou Medical University · CNChina Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveReactive oxygen species (ROS) are significantly upregulated after spinal cord injury (SCI). MicroRNAs (miRNAs) are reported to be widely involved in regulating gene expression. This paper aims to explore the correlation between ROS-induced cell apoptosis and abnormal miRNA expression after SCI.

methodsTo profile the expression of miRNAs after SCI, miRNA microarray was applied and the result was verified by reverse transcription quantitative PCR (RT-qPCR). ROS production following H

resultsMiR-200c was showed to be significantly increased after SCI by miRNA microassay and RT-qPCR. ROS production enhanced miR-200c expression in a dose-dependent manner and induced significant apoptosis in BV-2 cells. The upregulation of miR-200c reduced cell viability and induced BV-2 cell apoptosis. MiR-200c negatively regulated the expression of FAP-1, thereby inducing FAS signaling-induced apoptosis. RT-qPCR analysis showed that the FAP-1-targeting small interfering RNA (siRNA) did not affect the level of miR-200c in murine BV-2 cells. In addition, suppression of FAP-1 by siRNA promoted apoptosis, even in cells that were co-transfected with the miR-200c inhibitor.

conclusionsThe current data suggested that miR-200c contributes to apoptosis in murine BV-2 cells by regulating the expression of FAP-1. This proposes a therapeutic target for enhancing neural cell functional recovery after SCI.

Identifiers

PMID25448187
OpenAlexW2084419591

What OpenQuestion holds

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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.