Evidence map›Paper›PMID 30089893›Full record

ArticleSpinal cord2019

The protective effect of microRNA-21 in neurons after spinal cord injury.

Tao Zhang, Shuangfei Ni, Zixiang Luo, Ye Lang, Jianzhong Hu, Hongbin Lu

Open access · hybridAbstract read
In one paragraph

Article in Spinal cord, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

37 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Unravelling the novel insights between miR-7 and Parkinson's disease (PD).Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
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  17. Targeting miR-21 in spinal cord injuries: a game-changer?Molecular medicine (Cambridge, Mass.) · 2022
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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 at 3 institutions in 1 country.

Tao ZhangDepartment of Sports Medicine, Research Center of Sports Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Shuangfei NiDepartment of Spine Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Zixiang LuoDepartment of Spine Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Ye LangDepartment of Spine Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Jianzhong HuKey Laboratory of Organ Injury, Aging and Regenerative Medicine of Hunan Province, Changsha, Hunan, People's Republic of China.
Hongbin LuDepartment of Sports Medicine, Research Center of Sports Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China. hongbinlu@hotmail.com.
Xiangya Hospital Central South University · CNSoil and Fertilizer Institute of Hunan Province · CNCentral South University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81371956National Natural Science Foundation of China (National Science Foundation of China) 81672174
6 · The paper itself

Abstract

STUDY

designExperimental animal study.

objectivesTo validate the anti-apoptosis effect of microRNA-21 in neurons after spinal cord injury (SCI) and explore the mechanism.

settingXiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.

methodsIn situ hybridization was used to detect the expression of miR-21 in spinal cord neurons (n = 24). In a rat contusion SCI model (n = 48), we upregulated the miR-21 level around the injured area using miR-21 lentiviral vectors and evaluated the therapeutic effect with histology and behavioural scores. In neuronal cells, oxygen-glucose deprivation (OGD) was exerted to imitate SCI, and we explored the biomechanism using molecular biology and a dual-luciferase reporter assay.

resultsmiR-21 was expressed in spinal cord neurons and was found to improve neuronal survival and promote functional recovery in rat SCI models. The in vitro results in PC-12 cells revealed that the augmentation of endogenous miR-21 was able to reduce neuronal cell death after OGD. In addition, overexpression of miR-21 was able to reduce cellular apoptosis via decreasing PDCD4 protein levels, and caspase-3 activity was also influenced. Transfection of miR-21 into 293T cells was able to decrease luciferase activity in a reporter assay system, including the 3' untranslated region of PDCD4.

conclusionsmiR-21 may have a protective role in neuronal apoptosis after SCI. PDCD4 may be a functional target gene involved in the miR-21-mediated anti-apoptotic effect through an miR-21/PDCD4/caspase-3 pathway.

Indexed as

AnimalsApoptosisApoptosis Regulatory ProteinsCell CountDisease Models, AnimalHypoxiaMaleMicroRNAsMotor NeuronsOxygenPC12 CellsPhosphopyruvate HydrataseRatsRats, Sprague-DawleyRNA, MessengerSpinal Cord InjuriesApoptosis Regulatory ProteinsMicroRNAsmirn21 microRNA, ratOxygenPdcd4 protein, ratPhosphopyruvate HydrataseRNA, Messenger

Identifiers

PMID30089893
PMCPMC6358587
OpenAlexW2887419276

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.