Evidence map›Paper›PMID 30146926›Full record

ArticleCell cycle (Georgetown, Tex.)2018

LncRNA DGCR5 suppresses neuronal apoptosis to improve acute spinal cord injury through targeting PRDM5.

Huafeng Zhang, Wengang Wang, Ning Li, Peng Li, Ming Liu, Junwei Pan, Dan Wang, Junwei Li, Yuanyuan Xiong, Lei Xia

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
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  6. Review
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  11. Polydatin protects H9c2 cells from hypoxia-induced injury via up-regulating long non-coding RNA DGCR5.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2019
    Article
  12. Review
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

10 authors at 2 institutions in 1 country.

Huafeng Zhanga Department of Orthopedics , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Wengang Wanga Department of Orthopedics , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Ning Lia Department of Orthopedics , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Peng Lia Department of Orthopedics , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Ming Liua Department of Orthopedics , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Junwei Pana Department of Orthopedics , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Dan Wanga Department of Orthopedics , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Junwei Lia Department of Orthopedics , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
Yuanyuan Xiongb Department of Hematology , the Affiliated Cancer Hospital of Zhengzhou University and Henan Cancer Hospital , Zhengzhou , China.
Lei Xiaa Department of Orthopedics , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , China.
First Affiliated Hospital of Zhengzhou University · CNZhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal cord injury (SCI) usually results in neurological damage. DGCR5 is closely related to neurological disorders, and this study aims to explore its role in neuronal apoptosis in acute SCI. The ASCI model was established in rats, and the Basso, Beattie, and Bresnahan (BBB) scoring was used to assess the neurological function. The expression of RNA and protein was quantified by quantitative real-time PCR (qRT-PCR) and western blotting, respectively. The oxygenglucose deprivation (OGD) was performed upon neurons and apoptosis was evaluated by flow cytometry. The interaction and binding between DGCR5 and PRDM5 was detected with RNA pull-down and RIP assay, respectively. DGCR5 was down-regulated in ASCI model rat and in neurons treated with hypoxia. Over-expression of DGCR5 inhibited neuronal apoptosis. Interaction between DGCR5 negatively regulated PRDM5 protein expression by binding and interacting with it. DGCR5 inhibited neuronal apoptosis through PRDM5. Over-expressed DGCR5 ameliorated ASCI in rat. DGCR5 suppresses neuronal apoptosis through directly binding and negatively regulating PRDM5, and thereby ameliorating ASCI.

Indexed as

Acute DiseaseAnimalsApoptosisCell HypoxiaDisease Models, AnimalDown-RegulationNeuronsRats, Sprague-DawleyRNA, Long NoncodingSpinal Cord InjuriesTranscription FactorsPRDM5 protein, ratRNA, Long NoncodingTranscription FactorsAcute spinal cord injuryDGCR5neuronal apoptosisPR domain protein 5

Identifiers

PMID30146926
PMCPMC6224267
OpenAlexW2889312236

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.