Evidence map›Paper›PMID 25355277›Full record

ArticleInternational journal of molecular medicine2015

miRNA-130b is required for the ERK/FOXM1 pathway activation-mediated protective effects of isosorbide dinitrate against mesenchymal stem cell senescence induced by high glucose.

Jianfeng Xu, Zheyong Huang, Li Lin, Mingqiang Fu, Yanan Song, Yunli Shen, Daoyuan Ren, Yanhua Gao, Yangang Su, Yunzeng Zou and 5 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 33% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. In search of elixir: Pharmacological agents against stem cell senescence.Iranian journal of basic medical sciences · 2021
    Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Forkhead box M1 inhibits endothelial cell apoptosis and cell-cycle arrest through ROS generation.International journal of clinical and experimental pathology · 2018
    Article
  17. 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

15 authors at 5 institutions in 1 country.

Jianfeng XuDepartment of Cardiology, Minhang Hospital, Ruijin Hospital Group, Shanghai Jiaotong University School of Medicine, Shanghai 201199, P.R. China.
Zheyong HuangDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai 200032, P.R. China.
Li LinDepartment of Cardiology, Eastern Hospital, Tongji University, Shanghai 200120, P.R. China.
Mingqiang FuDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai 200032, P.R. China.
Yanan SongDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai 200032, P.R. China.
Yunli ShenDepartment of Cardiology, Eastern Hospital, Tongji University, Shanghai 200120, P.R. China.
Daoyuan RenDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai 200032, P.R. China.
Yanhua GaoDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai 200032, P.R. China.
Yangang SuDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai 200032, P.R. China.
Yunzeng ZouDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai 200032, P.R. China.
Yueguang ChenDepartment of Cardiology, Minhang Hospital, Ruijin Hospital Group, Shanghai Jiaotong University School of Medicine, Shanghai 201199, P.R. China.
Dadong ZhangDepartment of Cardiology, Minhang Hospital, Ruijin Hospital Group, Shanghai Jiaotong University School of Medicine, Shanghai 201199, P.R. China.
Wei HuDepartment of Cardiology, Minhang Hospital, Ruijin Hospital Group, Shanghai Jiaotong University School of Medicine, Shanghai 201199, P.R. China.
Juying QianDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai 200032, P.R. China.
Junbo GeDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai 200032, P.R. China.
Ruijin Hospital · CNZhongshan Hospital · CNSun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CNTongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study was carried out to investigate the hypothesis that organic nitrates can attenuate the senescence of mesenchymal stem cells (MSCs), a superior cell source involved in the regeneration and repair of damaged tissue. MSCs were treated with high glucose (HG) in order to induce senescence, which was markedly attenuated by pre-treatment with isosorbide dinitrate (ISDN), a commonly used nitrate, as indicated by senescence-associated galactosidase (SA-β-gal) activity, p21 expression, as well as by the mRNA levels of DNA methyltransferase 1 (DNMT1) and differentiated embryo chondrocyte expressed gene 1 (DEC1), which are senescence-related biomarkers. It was also found that the senescent MSCs (induced by HG glucose) exhibited a marked downregulation in ERK activity and forkhead box M1 (FOXM1) expression, which was reversed by ISDN preconditioning. Of note, the inhibition of ERK phosphorylation or the downregulation of FOXM1 statistically abolished the favourable effects of ISDN. In addition, the investigation of the senescence-associated miR-130 family suggested that miR-130b mediates the beneficial effects of ISDN; it was found that the protective effects of ISDN against the senescence of MSCs were prominently reversed by the knockdown of miR-130b. Furthermore, the downregulation of ERK phosphorylation or FOXM1 expression decreased the miR-130b expression level; however, the suppression of miR-130b demonstrated no significant impact on ERK phosphorylation or FOXM1 expression. Taken together, to the best of our knowledge, the present study is the first to demonstrate the favourable effects of ISDN against HG-induced MSC senescence, which are mediated through the activation of the ERK/FOXM1 pathway and the upregulation of miR-130b.

Indexed as

Signal TransductionAnimalsCells, CulturedCellular SenescenceExtracellular Signal-Regulated MAP KinasesForkhead Box Protein M1Forkhead Transcription FactorsGene Expression RegulationGlucoseIsosorbide DinitrateMaleMesenchymal Stem CellsMicroRNAsRatsExtracellular Signal-Regulated MAP KinasesForkhead Box Protein M1Forkhead Transcription FactorsFoxm1 protein, ratGlucoseIsosorbide DinitrateMicroRNAs

Identifiers

PMID25355277
PMCPMC4249746
OpenAlexW2004906344

What OpenQuestion holds

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LicenceCC BY
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.