Evidence map›Paper›PMID 30803283›Full record

ArticleThe Journal of international medical research2019

MicroRNA-590-5p antagonizes the inhibitory effect of high glucose on osteoblast differentiation by suppressing Smad7 in MC3T3-E1 cells.

Yinan Chen, Changhui Sun, Jiong Lu, Ling Zou, Minwei Hu, Zeyu Yang, Yaozeng Xu

Open access · goldAbstract read
In one paragraph

Article in The Journal of international medical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Role of microRNA in Diabetic Osteoporosis.Molecular biotechnology · 2025
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. The Role of MicroRNAs in Bone Metabolism and Disease.International journal of molecular sciences · 2020
    Review
  12. International journal of molecular sciences · 2019
    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 2 institutions in 1 country.

Yinan Chen1 Department of Orthopaedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Changhui Sun2 Department of Orthopaedics, Rui Jin Hospital Luwan Branch, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Jiong Lu2 Department of Orthopaedics, Rui Jin Hospital Luwan Branch, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Ling Zou2 Department of Orthopaedics, Rui Jin Hospital Luwan Branch, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Minwei Hu2 Department of Orthopaedics, Rui Jin Hospital Luwan Branch, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Zeyu Yang2 Department of Orthopaedics, Rui Jin Hospital Luwan Branch, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yaozeng Xu1 Department of Orthopaedics, The First Affiliated Hospital of Soochow University, Suzhou, China.ORCID https://orcid.org/0000-0002-7807-8604
Shanghai Jiao Tong University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveMicroRNA-590-5p (miR-590-5p) has been reported to stimulate osteoblast differentiation; however, its effect in diabetic osteoporosis remains unknown. This study investigated the effect of miR-590-5p on high glucose (HG)-suppressed osteoblast differentiation.

methodsThe effect of HG on MC3T3-E1 cell survival was assessed using the MTT assay. The expression levels and activities of osteoblastic proteins were evaluated by quantitative reverse transcription polymerase chain reaction (qRT-PCR), alkaline phosphatase (ALP) assay, and immunoblotting assay. Tumor growth factor-β (TGF-β) signaling in MC3T3-E1 cells was assessed using luciferase assay, qRT-PCR, and immunoblotting. Mineralized nodule formation in MC3T3-E1 cells was examined by using the mineralization assay.

resultsWhen MC3T3-E1 cells were exposed to HG conditions, there was significant downregulation of miR-590-5p and osteoblastic proteins (e.g., collagen I, Runx2, and ALP); in contrast, Smad7 was upregulated. Furthermore, miR-590-5p targeted Smad7 and inhibited its expression. Additionally, overexpression of miR-590-5p significantly promoted osteoblast growth and differentiation by upregulating TGF-β signaling in HG-treated MC3T3-E1 cells.

conclusionsCollectively, the results showed that miR-590-5p was involved in osteogenesis; moreover, miR-590-5p may represent a potential target for the treatment of diabetic osteoporosis.

Indexed as

Cell DifferentiationOsteogenesisAnimalsCells, CulturedGene Expression Regulation, NeoplasticGlucoseMiceMicroRNAsOsteoblastsSignal TransductionSmad7 ProteinGlucoseMicroRNAsMIRN590 microRNA, mouseSmad7 ProteinSmad7 protein, mousealkaline phosphatasediabeteshigh glucoseMC3T3-E1MicroRNA-590-5posteoblast differentiationosteoporosisSmad7tumor growth factor-β

Identifiers

PMID30803283
PMCPMC6460606
OpenAlexW2916374878

What OpenQuestion holds

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LicenceCC BY-NC
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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.