Evidence map›Paper›PMID 33270361›Full record

ArticleImmunity, inflammation and disease2021

Silenced SOX2-OT alleviates ventricular arrhythmia associated with heart failure by inhibiting NLRP3 expression via regulating miR-2355-3p.

Yuming Liang, Boqun Wang, Huijuan Huang, Maoyun Wang, Qianwen Wu, Yaxin Zhao, Yan He

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

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  10. Noncoding RNAs as Key Regulators for Cardiac Development and Cardiovascular Diseases.Journal of cardiovascular development and disease · 2023
    Review
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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.

Yuming LiangDepartment of Geriatrics Cardiology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Boqun WangDepartment of Geriatrics Cardiology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Huijuan HuangDepartment of Geriatrics Cardiology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Maoyun WangDepartment of Geriatrics Cardiology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Qianwen WuDepartment of Geriatrics Cardiology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yaxin ZhaoDepartment of Geriatrics Cardiology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yan HeDepartment of Geriatrics Cardiology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.ORCID 0000-0002-2402-0255
Guangxi Medical University · CN

Funding

National Natural Science Foundation of China 81760061
6 · The paper itself

Abstract

backgroundNucleotide-binding oligomerization domain-like receptor family pyrin domain containing 3 (NLRP3) inflammasomes are the most important factors in ventricular arrhythmia associated with heart failure (VA-HF). However, how the relationship between lncRNA and NLRP3 inflammasomes is regulated in VA-HF has not been investigated in detail. Thus, we aimed to determine the effects of SOX2-overlapping transcripts (SOX2-OT) by targeting NLRP3 in rats with VA-HF.

methodsWe established rats (SPF, male, weight: 240 ± 10 g) with VA-HF by aortic coarctation and constant-current stimulation, then injected them with small interfering SOX2-OT and anti-miR-2355-3p. Six weeks later, SOX2-OT and miR-2355-3p expression was measured using the quantitative reverse transcriptase-polymerase chain reaction and NLRP3, ASC, caspase-1, IL-1β, and TGF-β1 expression were measured by Western blot analysis; the ventricular chambers were histopathologically analyzed by staining with hematoxylin and eosin, Masson trichrome, and Picro Sirius Red and reactive oxygen species (ROS) levels were assessed by flow cytometry. The targeting relationship between miR-2355-3p and SOX2-OT or NLRP3 was verified using dual-luciferase reporter gene assays.

resultsThe expression of SOX2-OT and levels of NLRP3 inflammasomes gradually increased in normal rats, and in those with heart failure and with VA-HF. Silencing SOX2-OT expression inhibited NLRP3, ASC, caspase-1, IL-1β, and TGF-β1 expression and ROS production, reduced the degrees of cardiomyocyte necrosis and fibrosis and alleviated cardiac dysfunction in rats with VA-HF. MicroR-2355-3p can bind the SOX2-OT and the 3'-untranslated region of NLRP3. Inhibiting miR-2355-3p reversed the effect of SOX2-OT in rats with VA-HF.

conclusionsSilencing SOX2-OT alleviated cardiac dysfunction in rats by reducing the activation of NLRP3 inflammasomes via regulating miR-2355-3p.

Indexed as

Heart FailureMicroRNAsAnimalsArrhythmias, CardiacInflammasomesMaleNLR Family, Pyrin Domain-Containing 3 ProteinRatsInflammasomesMicroRNAsNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, ratarrhythmiasheart failureinflammasomelncRNAmicroRNAs

Identifiers

PMID33270361
PMCPMC7860601
OpenAlexW3108612134

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LicenceCC BY
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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.