Evidence map›Paper›PMID 28498451›Full record

ArticleMolecular medicine reports2017

Differential effects of p38 and Erk1/2 on the chondrogenic and osteogenic differentiation of dental pulp stem cells.

Pengfei Ba, Xiaoyu Duan, Guo Fu, Shuyan Lv, Pishan Yang, Qinfeng Sun

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  7. The Roles ofGenes · 2022
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  12. Role of long non-coding RNA H19 in the development of osteoporosis.Molecular medicine (Cambridge, Mass.) · 2021
    Review
  13. Article
  14. Article
  15. Dental-Derived Mesenchymal Stem Cells: State of the Art.Frontiers in cell and developmental biology · 2021
    Review
  16. Article
  17. Article
  18. Article
  19. Missense polymorphisms potentially involved in mandibular prognathism.Journal of oral biology and craniofacial research
    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

6 authors at 1 institution in 1 country.

Pengfei BaDepartment of Periodontology, School of Stomatology, Shandong University, Jinan, Shandong 250012, P.R. China.
Xiaoyu DuanNational Engineering Laboratory, WeGo Group Co., Ltd., Weihai, Shandong 264210, P.R. China.
Guo FuDepartment of Periodontology, Weihai Stomatological Hospital, Weihai, Shandong 264200, P.R. China.
Shuyan LvDepartment of Periodontology, Weihai Stomatological Hospital, Weihai, Shandong 264200, P.R. China.
Pishan YangDepartment of Periodontology, School of Stomatology, Shandong University, Jinan, Shandong 250012, P.R. China.
Qinfeng SunDepartment of Periodontology, School of Stomatology, Shandong University, Jinan, Shandong 250012, P.R. China.
Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The extracellular signal-regulated protein kinase 1/2 (Erk1/2) and p38 mitogen‑activated protein‑kinase pathways serve important roles in the regulation of osteogenic and chondrogenic differentiation in mesenchymal stem cells (MSCs). However, the exact mechanism remains unclear, and the effect is controversial. In the present study, the effects of Erk1/2 and p38 on the osteogenic and chondrogenic differentiation of dental pulp stem cells (DPSCs) were compared in vitro. The results indicated that inhibition of Erk1/2 is able to enhance the osteogenic differentiation of DPSCs and inhibit chondrogenic differentiation, whereas inhibition of p38 demonstrated the opposite effect. When compared with previous studies, the present study further confirmed that Erk1/2 and p38 serve important, but complicated, roles in regulating the differentiation of MSCs. Different chemical and physical stimuli, cell types, culture methods, times of inhibitor administration and the dosage of the inhibitor may influence the effect of Erk1/2 and p38 on the differentiation of MSCs. The present study aims to better understand the mechanisms that control the differentiation of MSCs and may be helpful in creating more effective tissue regeneration.

Indexed as

Cell DifferentiationBiomarkersCells, CulturedChondrogenesisDental PulpGene ExpressionHumansMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Osteogenesisp38 Mitogen-Activated Protein KinasesPhosphorylationStem CellsBiomarkersMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3p38 Mitogen-Activated Protein Kinases

Identifiers

PMID28498451
PMCPMC5482129
OpenAlexW2612762084

What OpenQuestion holds

Textmetadata
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.