Evidence map›Paper›PMID 41454344›Full record

ArticleBMC oral health2025

Effect of Enzymatic-based chemomechanical caries removal agent on proliferation and osteogenic differentiation of dental pulp stem cells.

Hend A Gouda, Hamdi H Hamama, Menatalla M Elhindawy, Asmaa S Elmahdy, Youssry M Elhawary

Abstract read
In one paragraph

Article in BMC oral health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Hend A GoudaFaculty of Dentistry, Mansoura University, Mansoura, Egypt.
Hamdi H HamamaFaculty of Dentistry, Mansoura University, Mansoura, Egypt. hamdy@connect.hku.hk.
Menatalla M ElhindawyFaculty of Dentistry, Mansoura University, Mansoura, Egypt.
Asmaa S ElmahdyFaculty of Dentistry, Mansoura University, Mansoura, Egypt.
Youssry M ElhawaryFaculty of Dentistry, Mansoura University, Mansoura, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChemomechanical caries removal (CMCR) offers a non-invasive alternative to conventional drilling techniques; however, the potential cytotoxic and genotoxic effects of CMCR agents on the dental pulp complex remain underexplored. This study aimed to evaluate the effects of enzymatic-based CMCR on the proliferation and osteogenic differentiation of dental pulp stem cells (DPSCs).

methodsMTT assay, scratch assay, and gene expression analysis were conducted to assess cell proliferation (viability percentage), migration (wound healing percentage), and osteogenic differentiation (RT-qPCR). The viability of DPSCs after direct exposure to enzymatic-based CMCR (0.5%, 1%, and 2% in DMEM) was measured at 24 and 48 h post-exposure. Indirect exposure was also tested using sound mineralized (0.5 mm and 1 mm) and demineralized (0.5 mm) dentin discs. Scratch assay was performed for control, direct, and indirect groups at 0, 24, and 48 h, followed by fixation and crystal violet staining at 48 h. Dentin sialophosphoprotein (DSPP) gene expression was quantified using RT-qPCR after 48 h.

resultsTwo-way ANOVA of proliferation and migration assays revealed that both indirect (0.5 mm demineralized dentin) and direct (0.5% DMEM) exposure groups showed the lowest cytotoxic effect after 24 h (82.75 ± 3.37 and 68.11 ± 4.99, respectively). After 48 h, a recovery trend in DPSC viability was observed, with both groups exhibiting the highest proliferation (93.60 ± 4.67 and 78.25 ± 4.88, respectively). These groups also showed the highest wound closure percentages (78.78 ± 0.89 for direct and 74.19 ± 1.03 for indirect exposure). One-way ANOVA of RT-qPCR results demonstrated significant upregulation of DSPP gene expression in the indirect (0.5 mm demineralized dentin) group (5.35 ± 2.01, p < 0.05).

conclusionEnzymatic-based CMCR exhibits favorable biocompatibility, particularly when applied directly on DPSCs at low concentrations and when used indirectly through dentin discs. These findings suggest that this enzymatic caries removal approach is potentially safe, effective, and minimally invasive, making it suitable for conservative restorative dentistry.

Indexed as

Cell DifferentiationCell ProliferationDental CariesDental Cavity PreparationDental PulpOsteogenesisStem CellsCell MovementCells, CulturedCell SurvivalExtracellular Matrix ProteinsGlutamic AcidHumansLeucineLysinePhosphoproteinsCarisolvExtracellular Matrix ProteinsGlutamic AcidLeucineLysinePhosphoproteinsSialoglycoproteinsAnd wound healingChemomechanical agentsDPSCsDSPPEnzymatic-based CMCRMTT

Identifiers

PMID41454344
PMCPMC12853919

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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.