Evidence map›Paper›PMID 30187276›Full record

ArticleJournal of bone and mineral metabolism2019

FGF2-responsive genes in human dental pulp cells assessed using a rat spinal cord injury model.

Ken Sugiyama, Kosuke Nagashima, Takahiro Miwa, Yuta Shimizu, Tomoko Kawaguchi, Kazuki Iida, Naritaka Tamaoki, Daijiro Hatakeyama, Hitomi Aoki, Chikara Abe and 5 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Journal of bone and mineral metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Human dental pulp stem cells for spinal cord injury.Stem cell research & therapy · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. 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

15 authors at 3 institutions in 1 country.

Ken SugiyamaDepartment of Oral and Maxillofacial Science, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Gifu, 501-1194, Japan.
Kosuke NagashimaLaboratory of Molecular Biology, Gifu Pharmaceutical University, 1-25-4 Daigaku-Nishi, Gifu, Gifu, 501-1196, Japan.
Takahiro MiwaLaboratory of Molecular Biology, Gifu Pharmaceutical University, 1-25-4 Daigaku-Nishi, Gifu, Gifu, 501-1196, Japan.
Yuta ShimizuDepartment of Periodontology, Asahi University School of Dentistry, 1851-1 Hozumi, Mizuho, Gifu, 501-0296, Japan.
Tomoko KawaguchiDepartment of Oral and Maxillofacial Science, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Gifu, 501-1194, Japan.
Kazuki IidaDepartment of Oral and Maxillofacial Science, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Gifu, 501-1194, Japan.
Naritaka TamaokiDepartment of Oral and Maxillofacial Science, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Gifu, 501-1194, Japan.
Daijiro HatakeyamaDepartment of Oral and Maxillofacial Science, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Gifu, 501-1194, Japan.
Hitomi AokiDepartment of Tissue and Organ Development, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Gifu, 501-1194, Japan.
Chikara AbeDepartment of Physiology, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Gifu, 501-1194, Japan.
Hironobu MoritaDepartment of Physiology, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Gifu, 501-1194, Japan.
Takahiro KunisadaDepartment of Tissue and Organ Development, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Gifu, 501-1194, Japan.
Toshiyuki ShibataDepartment of Oral and Maxillofacial Science, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Gifu, 501-1194, Japan.
Hidefumi FukumitsuLaboratory of Molecular Biology, Gifu Pharmaceutical University, 1-25-4 Daigaku-Nishi, Gifu, Gifu, 501-1196, Japan.
Ken-Ichi TezukaDepartment of Tissue and Organ Development, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Gifu, 501-1194, Japan. tezuka@gifu-u.ac.jp.ORCID http://orcid.org/0000-0002-0664-4080
Gifu University · JPGifu Pharmaceutical University · JPAsahi University · JP

Funding

Japan Society for the Promotion of Science JP17H06731Japan Society for the Promotion of Science JP23592697Japan Society for the Promotion of Science JP26293426Japan Society for the Promotion of Science JP26463000Japan Society for the Promotion of Science JP26463001Japan Society for the Promotion of Science JP26670799
6 · The paper itself

Abstract

The central nervous system in adult mammals does not heal spontaneously after spinal cord injury (SCI). However, SCI treatment has been improved recently following the development of cell transplantation therapy. We recently reported that fibroblast growth factor (FGF) 2-pretreated human dental pulp cells (hDPCs) can improve recovery in a rat model of SCI. This study aimed to investigate mechanisms underlying the curative effect of SCI enhanced via FGF2 pretreatment; we selected three hDPC lines upon screening for the presence of mesenchymal stem cell markers and of their functionality in a rat model of SCI, as assessed using the Basso, Beattie, and Bresnahan score of locomotor functional scale, electrophysiological tests, and morphological analyses. We identified FGF2-responsive genes via gene expression analyses in these lines. FGF2 treatment upregulated GABRB1, MMP1, and DRD2, which suggested to contribute to SCI or central the nervous system. In an expanded screening of additional lines, GABRB1 displayed rather unique and interesting behavior; two lines with the lowest sensitivity of GABRB1 to FGF2 treatment displayed an extremely minor effect in the SCI model. These findings provide insights into the role of FGF2-responsive genes, especially GABRB1, in recovery from SCI, using hDPCs treated with FGF2.

Indexed as

AnimalsDental PulpDisease Models, AnimalElectrophysiological PhenomenaFibroblast Growth Factor 2Gene Expression RegulationHumansMotor ActivityRatsRats, Sprague-DawleyRecovery of FunctionSpinal Cord InjuriesFibroblast Growth Factor 2Fibroblast growth factor 2GABRB1Human dental pulp cellsSpinal cord injury

Identifiers

PMID30187276
OpenAlexW2890196404

What OpenQuestion holds

Textmetadata
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.