Evidence map›Paper›PMID 27959394›Full record

ArticleInternational journal of molecular medicine2017

miR-214 suppresses the osteogenic differentiation of bone marrow-derived mesenchymal stem cells and these effects are mediated through the inhibition of the JNK and p38 pathways.

Yongzhi Guo, Lianhua Li, Jie Gao, Xiaobin Chen, Qinghua Sang

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Circular RNAs: Promising Targets in Osteoporosis.Current osteoporosis reports · 2023
    Review
  7. Review
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  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. The Role of MicroRNAs in Bone Metabolism and Disease.International journal of molecular sciences · 2020
    Review
  18. Article
  19. Article
  20. Roles of MicroRNAs in Bone Destruction of Rheumatoid Arthritis.Frontiers in cell and developmental biology · 2020
    Review
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 1 institution in 1 country.

Yongzhi GuoDepartment of Orthopedics, Beijing Army General Hospital, Dongcheng, Beijing 100700, P.R. China.
Lianhua LiDepartment of Orthopedics, Beijing Army General Hospital, Dongcheng, Beijing 100700, P.R. China.
Jie GaoDepartment of Orthopedics, Beijing Army General Hospital, Dongcheng, Beijing 100700, P.R. China.
Xiaobin ChenDepartment of Orthopedics, Beijing Army General Hospital, Dongcheng, Beijing 100700, P.R. China.
Qinghua SangDepartment of Orthopedics, Beijing Army General Hospital, Dongcheng, Beijing 100700, P.R. China.
The Military General Hospital of Beijing PLA · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we sought to investigate the expression of microRNA (miR)-214 on the osteogenic differentiation of bone marrow‑derived mesenchymal stem cells (BMSCs) and explore the possible underlying mechanisms. We found that the overexpression of miR‑214 effectively promoted the adipocyte differentiation of BMSCs in vitro, reduced alkaline phosphatase (ALP) activity and the gene expression of collagen type I (Col I), osteocalcin (OCN) and osteopontin (OPN) in the BMSCs. We further found that the overexpression of miR‑214 suppressed the protein expression of fibroblast growth factor (FGF), phosphorylated c‑Jun N-terminal kinase (p-JNK) and phosphorylated p38 (p-p38) in the BMSCs. The downregulation of miR‑214 promoted the osteogenic differentiation of BMSCs, and increased ALP activity and Col I, OCN and OPN gene expression in the BMSCs. It also increased FGF p-JNK and p-p38 protein expression in the BMSCs. The use of JNK inhibitor (SP600125) enhanced the inhibitory effects of miR‑214 overexpression on osteogenic differentiation, ALP activity, and Col I, OCN and OPN gene expression in the BMSCs. Lastly, the use of p38 inhibitor (SB202190) also enhanced the inhibitory effects of miR‑214 overexpression on ALP activity, and Col I, OCN and OPN gene expression in the BMSCs. These results provide a mechanism responsible for the suppressive effects of miR‑214 on the osteogenic differentiation of BMSCs involving the inhibition of the JNK and p38 pathways.

Indexed as

MAP Kinase Signaling SystemAdipocytesAlkaline PhosphataseAnimalsBone Marrow CellsCell DifferentiationCollagen Type IDown-RegulationFibroblast Growth FactorsJNK Mitogen-Activated Protein KinasesMaleMesenchymal Stem CellsMicroRNAsOsteocalcinOsteogenesisOsteopontinAlkaline PhosphataseCollagen Type IFibroblast Growth FactorsJNK Mitogen-Activated Protein KinasesMicroRNAsMirn214 microRNA, ratOsteocalcinOsteopontinp38 Mitogen-Activated Protein Kinases

Identifiers

PMID27959394
PMCPMC5179177
OpenAlexW2561525464

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.