Evidence map›Paper›PMID 27103465›Full record

ArticleStem cell research & therapy2016

microRNA-206 is involved in survival of hypoxia preconditioned mesenchymal stem cells through targeting Pim-1 kinase.

You Zhang, Wei Lei, Weiya Yan, Xizhe Li, Xiaolin Wang, Zhenao Zhao, Jie Hui, Zhenya Shen, Junjie Yang

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Pim Kinases: Important Regulators of Cardiovascular Disease.International journal of molecular sciences · 2023
    Review
  4. Review
  5. Article
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  18. Review
  19. Cellular Therapy for Sepsis: A New Hope?Critical care medicine · 2016
    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

9 authors at 3 institutions in 1 country.

You ZhangDepartment of Cardiology of the First Affiliated Hospital, Soochow University, Suzhou, China.
Wei LeiInstitute for Cardiovascular Science & Department of Cardiovascular Surgery of The First Affiliated Hospital, Soochow University, Suzhou, China.
Weiya YanInstitute for Cardiovascular Science & Department of Cardiovascular Surgery of The First Affiliated Hospital, Soochow University, Suzhou, China.
Xizhe LiDepartment of Cardiovascular Surgery, Affiliated Shanghai 1st People's Hospital, Shanghai Jiaotong University, Shanghai, China.
Xiaolin WangDepartment of Thoracic and Cardiovascular Surgery, Northern Jiangsu People's Hospital, Yangzhou, China.
Zhenao ZhaoInstitute for Cardiovascular Science & Department of Cardiovascular Surgery of The First Affiliated Hospital, Soochow University, Suzhou, China.
Jie HuiDepartment of Cardiology of the First Affiliated Hospital, Soochow University, Suzhou, China. huijie92@163.com.
Zhenya ShenInstitute for Cardiovascular Science & Department of Cardiovascular Surgery of The First Affiliated Hospital, Soochow University, Suzhou, China. uuzyshen@aliyun.com.
Junjie YangInstitute for Cardiovascular Science & Department of Cardiovascular Surgery of The First Affiliated Hospital, Soochow University, Suzhou, China. jjyang@suda.edu.cn.
First Affiliated Hospital of Soochow University · CNSoochow University · CNNorthern Jiangsu People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOverexpression of Pim-1 in stem/progenitor cells stimulated cell cycling and enhanced cardiac regeneration in vivo. We proposed that hypoxic preconditioning could increase survival of bone marrow mesenchymal stem cells (MSCs) via upregulation of Pim-1 and aimed to determine the microRNAs that modulate the expression of Pim-1. METHODS AND

resultsMSCs were subjected to hypoxia exposure. The expression of Pim-1 in MSCs was enhanced in a time-dependent manner, detected by quantitative PCR and western blot. miR-206 is predicted as one of the potential microRNAs that target Pim-1. The expression of miR-206 was decreased in hypoxic MSCs and reversely correlated with Pim-1 expression. Luciferase activity assay further confirmed Pim-1 as a putative target of miR-206. In addition, gain and loss-of-function studies with miR-206 mimics and inhibitors showed that inhibition of miR-206 in hypoxic MSCs promoted the migration ability of the cells, prevented cell apoptosis, and protected membrane potential of mitochondria, while the benefits were all blocked by Pim-1 inhibitor. In an acute model of myocardial infarction, transplanted hypoxic MSCs showed a significantly improved survival as compared with hypoxic MSCs overexpressing miR-206.

conclusionsHypoxic preconditioning could increase short-term survival of bone marrow MSCs via upregulation of Pim-1, and miR-206 was one of the critical regulators in this process.

Indexed as

Ischemic PreconditioningMesenchymal Stem Cell TransplantationAnimalsAntagomirsApoptosisCell HypoxiaCell MovementCell SurvivalDisease Models, AnimalFemaleGene Expression RegulationGenes, ReporterLuciferasesMaleMembrane Potential, MitochondrialMesenchymal Stem CellsAntagomirsLuciferasesMicroRNAsmirn206 microRNA, ratPim1 protein, ratProtein Kinase InhibitorsProto-Oncogene Proteins c-pim-1ApoptosisHypoxiaMesenchymal stem cellsmiR-206Pim-1

Identifiers

PMID27103465
PMCPMC4840980
OpenAlexW2339891804

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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.