Evidence map›Paper›PMID 31877561›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2019

Concentrated Growth Factor Promotes Dental Pulp Cells Proliferation and Mineralization and Facilitates Recovery of Dental Pulp Tissue.

Songbo Tian, Jie Wang, Fusheng Dong, Nan Du, Wenjing Li, Peng Song, Yanping Liu

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2019. 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
4.9field-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

19 citing papers in PubMed, 36 citations in OpenAlex.

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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.

Songbo TianDepartment of Oral Medicine, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China (mainland).
Jie WangDepartment of Oral Pathology, College of Stomatology, Hebei Medical University, Shijiazhuang, Hebei, China (mainland).
Fusheng DongDepartment of Oral and Maxillofacial Surgery, College of Stomatology, Hebei Medical University, Shijiazhuang, Hebei, China (mainland).
Nan DuDepartment of Oral Medicine, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China (mainland).
Wenjing LiDepartment of Oral Medicine, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China (mainland).
Peng SongDepartment of Oral Pathology, College of Stomatology, Hebei Medical University, Shijiazhuang, Hebei, China (mainland).
Yanping LiuPhysical Examination Center, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China (mainland).
Hebei Medical University · CNSecond Hospital of Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Dental pulp cells (DPCs) play vital roles in the recovery of dental pulp tissue. Concentrated growth factor (CGF) can promote proliferation and mineralization of various cells. However, the functions of CGF on DPCs and dental pulp tissue are unclear. The object of our study was to identify the roles of CGF in DPCs proliferation and mineralization in vitro and to assess the effects of CGF on direct pulp capping in vivo. MATERIAL AND METHODS We performed CCK-8 and Transwell assay to detect proliferation and migration activity of DPCs. Alizarin Red staining was performed to examine mineralized nodules. Alkaline phosphatase activity test was used to measure the mineralization capacity of DPCs. We assessed the odontogenic differentiation gene expression level by Western blot and qPCR. The effect of CGF on direct pulp capping in vivo were evaluated by radiography and histopathology. RESULTS CGF increased the number of proliferative and migratory DPCs. CGF enhanced DPCs mineralized nodules and improved the gene expression levels of DSPP, DMP-1, BSP, and ALP. CGF upregulated the protein levels of ALP, BMP2, SMAD5, Runx2, and p-Smad, and the effect could be partially reversed by Noggin. CGF promoted pulp recovery and kept its vitality in directly pulp capping. CONCLUSIONS CGF promotes DPCs proliferation and mineralization. It regulates the mineralization of DPCs via the BMP2/SMAD5/Runx2 signaling pathway. CGF can be used as the effective graft for direct pulp capping.

Indexed as

AdolescentAdultCalcification, PhysiologicCell DifferentiationCell ProliferationDental PulpFemaleHumansIntercellular Signaling Peptides and ProteinsMaleMolar, ThirdPlatelet-Derived Growth FactorPrimary Cell CultureToothYoung AdultIntercellular Signaling Peptides and ProteinsPlatelet-Derived Growth Factor

Identifiers

PMID31877561
PMCPMC6944166
OpenAlexW2998281820

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.