Evidence map›Paper›PMID 26717909›Full record

ArticlePediatric cardiology2016

MiRNA-145 Regulates the Development of Congenital Heart Disease Through Targeting FXN.

Lei Wang, Danqiu Tian, Jihua Hu, Haijian Xing, Min Sun, Juanli Wang, Qiang Jian, Hua Yang

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric cardiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.5field-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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Role of miRNA in Cardiovascular Diseases in Children-Systematic Review.International journal of molecular sciences · 2024
    Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. The diagnostic value of circulating microRNAs in heart failure.Experimental and therapeutic medicine · 2019
    Review
  11. Article
  12. [Research progress on genetic and epigenetic mechanisms in congenital heart disease].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2018
    Review
  13. 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

8 authors at 1 institution in 1 country.

Lei WangDepartment of Cardiology, Xi'an Children's Hospital, No. 69, Xiju RD, Lianhu District, Xi'an, 710003, Shaanxi, China. xawanglei@163.com.
Danqiu TianDepartment of Cardiology, Xi'an Children's Hospital, No. 69, Xiju RD, Lianhu District, Xi'an, 710003, Shaanxi, China.
Jihua HuDepartment of Cardiology, Xi'an Children's Hospital, No. 69, Xiju RD, Lianhu District, Xi'an, 710003, Shaanxi, China.
Haijian XingDepartment of Cardiology, Xi'an Children's Hospital, No. 69, Xiju RD, Lianhu District, Xi'an, 710003, Shaanxi, China.
Min SunDepartment of Cardiology, Xi'an Children's Hospital, No. 69, Xiju RD, Lianhu District, Xi'an, 710003, Shaanxi, China.
Juanli WangDepartment of Cardiology, Xi'an Children's Hospital, No. 69, Xiju RD, Lianhu District, Xi'an, 710003, Shaanxi, China.
Qiang JianDepartment of Cardiology, Xi'an Children's Hospital, No. 69, Xiju RD, Lianhu District, Xi'an, 710003, Shaanxi, China.
Hua YangDepartment of Cardiology, Xi'an Children's Hospital, No. 69, Xiju RD, Lianhu District, Xi'an, 710003, Shaanxi, China.
Xi’an Children’s Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital heart disease (CHD) is the leading cause of death in infants in the world. The study of CHDs has come a long way since their classification and description. Although transcriptional programmes that are impaired in individuals with CHDs are being identified, the mechanisms of how these deficiencies translate to a structural defect are unknown. In this study, using high-throughput microarray analysis and molecular network analysis, FXN was identified to be the most differentially expressed key gene in CHD. By TargetScan analysis, we predicted FXN was the target gene of miRNA-145 and miRNA-182. Through real-time PCR analysis of clinical samples and experiments in cell lines, we confirmed that miRNA-145 but not miRNA-182 directly binds to the 3' UTR region of FXN and negatively regulates its expression. We further found that through targeting FXN, miRNA-145 regulates apoptosis and mitochondrial function. In general, our study confirmed the differentially expressed FXN regulates the development of CHD and the differential expression was under the control of miRNA-145. These results might provide new insight into the understanding of the CHD pathogenesis and may facilitate further therapeutic studies.

Indexed as

3' Untranslated RegionsCase-Control StudiesChildChild, PreschoolChinaFemaleFrataxinGene Regulatory NetworksHeart Defects, CongenitalHumansIron-Binding ProteinsMaleMicroarray AnalysisMicroRNAs3' Untranslated RegionsFrataxinIron-Binding ProteinsMicroRNAsMIRN145 microRNA, humanCongenital heart diseaseFXNMiRNA-145

Identifiers

PMID26717909
OpenAlexW2196769224

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.