Evidence map›Paper›PMID 27731397›Full record

ArticleScientific reports2016

Role of Mir-155 in Controlling HIF-1α Level and Promoting Endothelial Cell Maturation.

Deguang Yang, Jinhong Wang, Meng Xiao, Tao Zhou, Xu Shi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

38 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  11. Drug design, development and therapy · 2023
    Article
  12. Review
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  15. Review
  16. M2 Macrophage-Derived Exosomes Promote Angiogenesis and Growth of Pancreatic Ductal Adenocarcinoma by Targeting E2F2.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  17. microRNA-155-3p attenuates intervertebral disc degeneration via inhibition of KDM3A and HIF1α.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
    Article
  18. Article
  19. Article
  20. Experimental and therapeutic medicine · 2020
    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

5 authors at 2 institutions in 1 country.

Deguang YangDepartment of Cardiology, the Third Affiliated Hospital of Southern Medical University, Guangzhou, 510000, China.
Jinhong WangDepartment of Respiration, the Third Affiliated Hospital of Southern Medical University, Guangzhou, 510000, China.
Meng XiaoDepartment of Nursing, the Third Affiliated Hospital of Southern Medical University, Guangzhou, 510000, China.
Tao ZhouDepartment of Cardiology, the Third Affiliated Hospital of Southern Medical University, Guangzhou, 510000, China.
Xu ShiCentral Laboratory, the First Hospital of Jilin University, Changchun, 130032, China.
Third Affiliated Hospital of Southern Medical University · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stem-cell-based therapy for cardiovascular disease, especially ischemic heart disease (IHD), is a promising approach to facilitating neovascularization through the migration of stem cells to the ischemic site and their subsequent differentiation into endothelial cells (ECs). Hypoxia is a chief feature of IHD and the stem cell niche. However, whether hypoxia promotes stem cell differentiation into ECs or causes them to retain their stemness is controversial. Here, the differentiation of pluripotent stem cells (iPSCs) into endothelial cells (ECs) was induced under hypoxia. Though the angiogenic capability and angiogenesis-related autocrine/paracrine factors of the ECs were improved under hypoxia, the level of hypoxia inducible factor 1α (HIF-1α) was nonetheless found to be restricted along with the EC differentiation. The down-regulation of HIF-1α was found to have been caused by VEGF-induced microRNA-155 (miR-155). Moreover, miR-155 was also found to enhance the angiogenic capability of induced ECs by targeting E2F2 transcription factor. Hence, miR-155 not only contributes to controlling HIF-1α expression under hypoxia but also promotes angiogenesis, which is a key feature of mature ECs. Revealing the real role of hypoxia and clarifying the function of miR-155 in EC differentiation may facilitate improvement of angiogenic gene- and stem-cell-based therapies for ischemic heart disease.

Indexed as

AnimalsBase SequenceCell DifferentiationCell HypoxiaCell LineE2F2 Transcription FactorEndothelial CellsFeeder CellsFibroblastsGene Expression RegulationHumansHuman Umbilical Vein Endothelial CellsHypoxia-Inducible Factor 1, alpha SubunitInduced Pluripotent Stem CellsMiceMicroRNAsE2F2 protein, humanE2F2 Transcription FactorHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMicroRNAsMIRN155 microRNA, humanVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID27731397
PMCPMC5059686
OpenAlexW2529878187

What OpenQuestion holds

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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.