Evidence map›Paper›PMID 24809979›Full record

ArticlePloS one2014

Proteomic analysis of mesenchymal stem cells from normal and deep carious dental pulp.

Dandan Ma, Li Cui, Jie Gao, Wenjuan Yan, Ying Liu, Shuaimei Xu, Buling Wu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. 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
1.3field-weighted citation impact, top 20% 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, 26 citations in OpenAlex.

  1. A scoping review of proteomic alterations in molar-incisor hypomineralisation: insights from enamel and salivary composition.European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry · 2025
    Article
  2. Review
  3. Stem cell therapy for regenerating periodontal bony defects: A narrative review.Journal of advanced periodontology & implant dentistry · 2025
    Review
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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.

Dandan MaDepartment of Stomatology, Nanfang Hospital, Guangzhou, P.R. China; College of Stomatology, Southern Medical University, Guangzhou, P.R. China.
Li CuiDepartment of Stomatology, Nanfang Hospital, Guangzhou, P.R. China; College of Stomatology, Southern Medical University, Guangzhou, P.R. China.
Jie GaoDepartment of Stomatology, Nanfang Hospital, Guangzhou, P.R. China; College of Stomatology, Southern Medical University, Guangzhou, P.R. China.
Wenjuan YanDepartment of Stomatology, Nanfang Hospital, Guangzhou, P.R. China; College of Stomatology, Southern Medical University, Guangzhou, P.R. China.
Ying LiuDepartment of Stomatology, Nanfang Hospital, Guangzhou, P.R. China; College of Stomatology, Southern Medical University, Guangzhou, P.R. China.
Shuaimei XuDepartment of Stomatology, Nanfang Hospital, Guangzhou, P.R. China; College of Stomatology, Southern Medical University, Guangzhou, P.R. China.
Buling WuDepartment of Stomatology, Nanfang Hospital, Guangzhou, P.R. China; College of Stomatology, Southern Medical University, Guangzhou, P.R. China.
Southern Medical University · CNNanfang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dental pulp stem cells (DPSCs), precursor cells of odontoblasts, are ideal seed cells for tooth tissue engineering and regeneration. Our previous study has demonstrated that stem cells exist in dental pulp with deep caries and are called carious dental pulp stem cells (CDPSCs). The results indicated that CDPSCs had a higher proliferative and stronger osteogenic differentiation potential than DPSCs. However, the molecular mechanisms responsible for the biological differences between DPSCs and CDPSCs are poorly understood. The aim of this study was to define the molecular features of DPSCs and CDPSCs by comparing the proteomic profiles using two-dimensional fluorescence difference gel electrophoresis (2-D DIGE) in combination with matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS). Our results revealed that there were 18 protein spots differentially expressed between DPSCs and CDPSCs in a narrow pH range of 4 to 7. These differently expressed proteins are mostly involved in the regulation of cell proliferation, differentiation, cell cytoskeleton and motility. In addition, our results suggested that CDPSCs had a higher expression of antioxidative proteins that might protect CDPSCs from oxidative stress. This study explores some potential proteins responsible for the biological differences between DPSCs and CDPSCs and expands our understanding on the molecular mechanisms of mineralization of DPSCs in the formation of the dentin-pulp complex.

Indexed as

ProteomicsAdolescentCell DifferentiationCell ProliferationDental CariesDental PulpHumansHydrogen-Ion ConcentrationMesenchymal Stem CellsYoung Adult

Identifiers

PMID24809979
PMCPMC4014579
OpenAlexW2094886860

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.