Evidence map›Paper›PMID 29227539›Full record

ArticleJournal of cellular biochemistry2018

Mir-29b promotes human aortic valve interstitial cell calcification via inhibiting TGF-β3 through activation of wnt3/β-catenin/Smad3 signaling.

Ming Fang, Cheng-Guang Wang, Changzhu Zheng, Jun Luo, Shiqiang Hou, Kangyong Liu, Xinming Li

Open access · hybridAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. The role of microRNAs in calcific aortic valve disease.Frontiers in cardiovascular medicine · 2025
    Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Matters of the heart: Cellular sex differences.Journal of molecular and cellular cardiology · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. The Role of Wnt/β-Catenin Pathway Mediators in Aortic Valve Stenosis.Frontiers in cell and developmental biology · 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 3 institutions in 1 country.

Ming FangDepartment of Cardiology, Hainan General Hospital, Haikou, Hainan, P.R. China.
Cheng-Guang WangLaboratory of System Biology, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, P.R. China.
Changzhu ZhengDepartment of Cardiology, Shanghai Zhoupu Hospital, Shanghai, P.R. China.
Jun LuoDepartment of Cardiology, Shanghai Zhoupu Hospital, Shanghai, P.R. China.
Shiqiang HouDepartment of Cardiology, Shanghai Zhoupu Hospital, Shanghai, P.R. China.
Kangyong LiuDepartment of Neurology, Shanghai Zhoupu Hospital, Shanghai, P.R. China.
Xinming LiDepartment of Cardiology, Shanghai Zhoupu Hospital, Shanghai, P.R. China.ORCID 0000-0002-4213-4977
Shanghai University of Medicine and Health Sciences · CNChinese Academy of Sciences · CNHainan General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein, we hypothesized that pro-osteogenic MicroRNAs (miRs) could play functional roles in the calcification of the aortic valve and aimed to explore the functional role of miR-29b in the osteoblastic differentiation of human aortic valve interstitial cells (hAVICs) and the underlying molecular mechanism. Osteoblastic differentiation of hAVICs isolated from human calcific aortic valve leaflets obtained intraoperatively was induced with an osteogenic medium. Alizarin red S staining was used to evaluate calcium deposition. The protein levels of osteogenic markers and other proteins were evaluated using western blotting and/or immunofluorescence while qRT-PCR was applied for miR and mRNA determination. Bioinformatics and luciferase reporter assay were used to identify the possible interaction between miR-29b and TGF-β3. Calcium deposition and the number of calcification nodules were pointedly and progressively increased in hAVICs during osteogenic differentiation. The levels of osteogenic and calcification markers were equally increased, thus confirming the mineralization of hAVICs. The expression of miR-29b was significantly increased during osteoblastic differentiation. Furthermore, the osteoblastic differentiation of hAVICs was significantly inhibited by the miR-29b inhibition. TGF-β3 was markedly downregulated while Smad3, Runx2, wnt3, and β-catenin were significantly upregulated during osteogenic induction at both the mRNA and protein levels. These effects were systematically induced by miR-29b overexpression while the inhibition of miR-29b showed the inverse trends. Moreover, TGF-β3 was a direct target of miR-29b. Inhibition of miR-29b hinders valvular calcification through the upregulation of the TGF-β3 via inhibition of wnt/β-catenin and RUNX2/Smad3 signaling pathways.

Indexed as

AgedAged, 80 and overAortic ValveAortic Valve Stenosisbeta CateninCalcinosisCell DifferentiationCell LineFemaleHumansMaleMicroRNAsMiddle AgedSignal TransductionSmad3 ProteinTransforming Growth Factor beta3beta CateninMicroRNAsMIRN29a microRNA, humanSmad3 ProteinSMAD3 protein, humanTransforming Growth Factor beta3Wnt3 ProteinWNT3 protein, humancalcific aortic valve diseasemiR-29bRunx2/Smad3/TGF-β3 signalingvalvular calcificationwnt/β-catenin signaling

Identifiers

PMID29227539
PMCPMC6001435
OpenAlexW2772111099

What OpenQuestion holds

Textmetadata
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.