Evidence map›Paper›PMID 31773669›Full record

ArticleEuropean review for medical and pharmacological sciences2019

MicroRNA-15a inhibits inflammatory response and apoptosis after spinal cord injury via targeting STAT3.

W-D Wu, L-H Wang, N-X Wei, D-H Kong, G Shao, S-R Zhang, Y-S Du

Open access · greenAbstract read
In one paragraph

Article in European review for medical and pharmacological sciences, 2019. 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
1.8field-weighted citation impact, top 14% 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, 19 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 1 institution in 1 country.

W-D WuAnesthesiology Department, Danyang People's Hospital of Jiangsu Province & Danyang Hospital Affiliated to Nantong University, Danyang, Jiangsu, China. jsdywwd@163.com.
L-H Wang
N-X Wei
D-H Kong
G Shao
S-R Zhang
Y-S Du
Fuyang City People's Hospital · CN

Funding

Lead Exposure and Beta-Amyloid Transport by Brain BarriersR01ES027078 · NIEHS · PURDUE UNIVERSITY · PI DU, YANSHENG, ZHENG, WEI · 2017 to 2021
$2.2M
NIEHS NIH HHS R01 ES027078
6 · The paper itself

Abstract

objectiveTo clarify the function of microRNA-15a in the spinal cord injury (SCI) and its potential mechanism. PATIENTS AND

methodsThe plasma levels of microRNA-15a and signal transducer and activator of transcription 3 (STAT3) in SCI patients were determined by quantitative Real Time-Polymerase Chain Reaction (qRT-PCR). The correlation between the expressions of microRNA-15a and STAT3 was analyzed. The in vitro SCI model was established in H2O2-induced C8-D1A and C8B4 cells, and in vivo SCI model was established in mice by hitting T10. The mRNA and protein expressions of tumor necrosis factor-α (TNF-α) and interleukin 6 (IL-6) were detected in the SCI model. The apoptosis was examined by flow cytometry or TUNEL staining, respectively. The motor function of mouse hindlimb was evaluated using the Basso Beattie Bresnahan (BBB) standard scale. The target gene of microRNA-15a was predicted by bioinformatics and further verified by dual-luciferase reporter gene assay. The expression changes of target genes in C8-D1A and C8B4 cells with microRNA-15a overexpression or knockdown were examined by qRT-PCR and Western blot. Finally, rescue experiments were performed to evaluate the regulatory effects of microRNA-15a and STAT3 on cell apoptosis.

resultsMicroRNA-15a was lowly expressed in plasma of SCI patients, while STAT3 was highly expressed with a negative correlation to microRNA-15a. Identically, microRNA-15a was lowly expressed in H2O2-induced C8-D1A and C8B4 cells, and STAT3 was highly expressed. MicroRNA-15a overexpression downregulated mRNA and protein levels of TNF-α and IL-6 in C8-D1A and C8B4 cells. BBB score was markedly low in SCI mice relative to controls. SCI mice injected with microRNA-15a mimics had higher BBB score than those injected with negative control. Besides, SCI mice with microRNA-15a overexpression had downregulated expressions of STAT3, TNF-α, and IL-6 in the impaired spinal cord tissues, as well as lower apoptotic rate. Through bioinformatics, we found binding sites between STAT3 and microRNA-15a. Their binding conditions were further verified by dual-luciferase reporter gene assay. Moreover, STAT3 expression was negatively regulated by microRNA-15a. Finally, rescue experiments showed that STAT3 overexpression could reverse the regulatory effects of microRNA-15a on expressions of TNF-α and IL-6, as well as apoptosis.

conclusionsMicroRNA-15a expression decreases in the SCI model, which participates in the process of SCI by regulating inflammatory response and cell apoptosis via targeting STAT3.

Indexed as

AnimalsApoptosisCells, CulturedGene Knockdown TechniquesHindlimbHumansHydrogen PeroxideInflammationInterleukin-6MaleMiceMicroRNAsSpinal Cord InjuriesSTAT3 Transcription FactorTumor Necrosis Factor-alphaHydrogen PeroxideInterleukin-6MicroRNAsMirn15a microRNA, mouseSTAT3 Transcription FactorTumor Necrosis Factor-alpha

Identifiers

PMID31773669
PMCPMC7415187
OpenAlexW3004869424

What OpenQuestion holds

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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.