Evidence map›Paper›PMID 30669342›Full record

ArticleInternational journal of molecular sciences2019

ADAR1p150 Forms a Complex with Dicer to Promote miRNA-222 Activity and Regulate PTEN Expression in CVB3-Induced Viral Myocarditis.

Xincai Zhang, Xiangting Gao, Jun Hu, Yuxin Xie, Yuanyi Zuo, Hongfei Xu, Shaohua Zhu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

23 citing papers in PubMed, 92 citations in OpenAlex.

  1. Review
  2. The role of ADAR1 in human pathophysiology.Frontiers in cell and developmental biology · 2025
    Review
  3. Article
  4. Article
  5. RNA binding proteins in cardiovascular development and disease.Current topics in developmental biology · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Processing ofRNA (New York, N.Y.) · 2020
    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

7 authors at 2 institutions in 1 country.

Xincai ZhangInstitute of Forensic Medicine, Soochow University, Suzhou 215021, China. xczhang1@stu.suda.edu.cn.
Xiangting GaoDepartment of Pathology, School of Medicine, Shihezi University, Shihezi 215021, China. 20154221095@stu.suda.edu.cn.
Jun HuInstitute of Forensic Medicine, Soochow University, Suzhou 215021, China. 11916@jsmc.edu.cn.
Yuxin XieInstitute of Forensic Medicine, Soochow University, Suzhou 215021, China. yxxie@stu.suda.edu.cn.
Yuanyi ZuoInstitute of Forensic Medicine, Soochow University, Suzhou 215021, China. snxie@stu.suda.edu.cn.
Hongfei XuInstitute of Forensic Medicine, Soochow University, Suzhou 215021, China. xuhongfei@suda.edu.cn.
Shaohua ZhuInstitute of Forensic Medicine, Soochow University, Suzhou 215021, China. zhushaohua@suda.edu.cn.
Soochow University · CNShihezi University · CN

Funding

National Natural Science Foundation of China 81571848the Science Foundation of Suzhou,China sys2018056
6 · The paper itself

Abstract

Adenosine deaminases acting on RNA (ADAR) are enzymes that regulate RNA metabolism through post-transcriptional mechanisms. ADAR1 is involved in a variety of pathological conditions including inflammation, cancer, and the host defense against viral infections. However, the role of ADAR1p150 in vascular disease remains unclear. In this study, we examined the expression of ADAR1p150 and its role in viral myocarditis (VMC) in a mouse model. VMC mouse cardiomyocytes showed significantly higher expression of ADAR1p150 compared to the control samples. Coimmunoprecipitation verified that ADAR1p150 forms a complex with Dicer in VMC. miRNA-222, which is involved in many cardiac diseases, is highly expressed in cardiomyocytes in VMC. In addition, the expression of miRNA-222 was promoted by ADAR1p150/Dicer. Among the target genes of miRNA-222, the expression of phosphatase-and-tensin (PTEN) protein was significantly reduced in VMC. By using a bioinformatics tool, we found a potential binding site of miRNA-222 on the PTEN gene's 3'-UTR, suggesting that miRNA-222 might play a regulatory role. In cultured cells, miR-222 suppressed PTEN expression. Our findings suggest that ADAR1p150 plays a key role in complexing with Dicer and promoting the expression of miRNA-222, the latter of which suppresses the expression of the target gene PTEN during VMC. Our work reveals a previously unknown role of ADAR1p150 in gene expression in VMC.

Indexed as

Enterovirus B, HumanAdenosine DeaminaseAnimalsCells, CulturedCell SurvivalCoxsackievirus InfectionsDisease Models, AnimalGene ExpressionGene Expression RegulationGene Knockout TechniquesImmunohistochemistryMaleMiceMicroRNAsMyocarditisMyocardiumADAR1 protein, mouseAdenosine DeaminaseMicroRNAsMIRN222 microRNA, mousePTEN PhosphohydrolaseRibonuclease IIIADAR1p150miRNA-222PTENviral myocarditis

Identifiers

PMID30669342
PMCPMC6359435
OpenAlexW2908655219

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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.