Evidence map›Paper›PMID 32350569›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2020

LncRNA promoted inflammatory response in ischemic heart failure through regulation of miR-455-3p/TRAF6 axis.

Qianqian Gu, Bin Wang, Hongying Zhao, Wenjuan Wang, Pengsheng Wang, Yu Deng

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Vitamin D Reprograms Non-Coding RNA Networks to Block Zika Virus in Human Macrophages.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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 1 institution in 1 country.

Qianqian GuDepartment of Geriatrics, Cangzhou Central Hospital, 16 Xinhua West Road, Cangzhou, 061000, Hebei, China. QianqianGuqsc@163.com.ORCID http://orcid.org/0000-0001-9405-9131
Bin WangDepartment of Otorhinolaryngology, Cangzhou Central Hospital, Cangzhou, 061000, Hebei, China.
Hongying ZhaoDepartment of Geriatrics, Cangzhou Central Hospital, 16 Xinhua West Road, Cangzhou, 061000, Hebei, China.
Wenjuan WangDepartment of Geriatrics, Cangzhou Central Hospital, 16 Xinhua West Road, Cangzhou, 061000, Hebei, China.
Pengsheng WangDepartment of Geriatrics, Cangzhou Central Hospital, 16 Xinhua West Road, Cangzhou, 061000, Hebei, China.
Yu DengDepartment of Geriatrics, Cangzhou Central Hospital, 16 Xinhua West Road, Cangzhou, 061000, Hebei, China.
Cangzhou Central Hospital · CN

Funding

the Key Research and Development Plan Guidance Project of Cangzhou 172302054
6 · The paper itself

Abstract

objectivesIschemic heart failure (IHF) is the most common cause of death globally. Growing evidence shows abnormal expression of long non-coding RNAs in heart failure patients. This study aims to investigate the effect of sex-determining region Y-box 2 (SOX2) overlapping transcript (SOX2-OT) on the regulation of the inflammatory response in ischemic heart failure.

methodsIHF rat and oxygen and glucose deprivation (OGD) cell models were established. qRT-PCR was employed to investigate the expression of SOX2-OT. ELISA, western blot and cell viability/apoptosis assays were performed to assess the effects of SOX2-OT. Online software program was used to identify miRNAs that target SOX2-OT, followed by validation using RNA pull-down. Potential targets of miRNAs were searched, and examined by immunoblotting, qRT-PCR and luciferase reporter assay.

resultsSOX2-OT was up-regulated in IHF and OGD. Knockdown of SOX2-OT promoted cell proliferation, decreased apoptosis rate and cell oxidative damage, and ameliorated inflammatory response. SOX2-OT contains binding sites for miR-455-3p, miR-5586-3p and miR-1252-5p. RNA pull-down confirmed the binding ability between SOX2-OT and miR-455-3p. TRAF6 is a direct target of miR-455-3p. Moreover, the regulatory activity of SOX2-OT on inflammatory response was partially through its negative regulation of miR-455-3p, which directly regulates TRAF6. Down-regulation of SOX2-OT improved myocardial dysfunction in IHF rat.

conclusionsOur results reveal that SOX2-OT may be a driver of IHF through repression of miR-455-3p, and miR-455-3p alleviates IHF by targeting TRAF6. Therefore, SOX2-OT/miR-455-3p/TRAF6 may be a potential target for advanced therapeutic strategy for IHF.

Indexed as

AnimalsBinding SitesCell LineGene Expression RegulationGene Knockdown TechniquesHeart FailureInflammationMaleMicroRNAsMyocardial IschemiaMyocytes, CardiacRatsRats, Sprague-DawleyRNA, Long NoncodingTNF Receptor-Associated Factor 6Transfectionlong non-coding RNA Sox2ot, humanMicroRNAsMIRN455 microRNA, humanRNA, Long NoncodingTNF Receptor-Associated Factor 6Inflammatory responseIschemic heart failureNF-κbSOX2-OTTRAF6

Identifiers

PMID32350569
OpenAlexW3022641713

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.