Biomolecule-Mediated Therapeutics of the Dentin-Pulp Complex: A Systematic Review

Biomolecules. 2022 Feb 9;12(2):285. doi: 10.3390/biom12020285.

Abstract

The aim of this systematic review was to evaluate the application of potential therapeutic signaling molecules on complete dentin-pulp complex and pulp tissue regeneration in orthotopic and ectopic animal studies. A search strategy was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement in the MEDLINE/PubMed database. Animal studies evaluating the application of signaling molecules to pulpectomized teeth for pulp tissue or dentin-pulp complex regeneration were included. From 2530 identified records, 18 fulfilled the eligibility criteria and were subjected to detailed qualitative analysis. Among the applied molecules, basic fibroblast growth factor, vascular endothelial growth factor, bone morphogenetic factor-7, nerve growth factor, and platelet-derived growth factor were the most frequently studied. The clinical, radiographical and histological outcome measures included healing of periapical lesions, root development, and apical closure, cellular recolonization of the pulp space, ingrowth of pulp-like connective tissue (vascularization and innervation), mineralized dentin-like tissue formation along the internal dentin walls, and odontoblast-like cells in contact with the internal dentin walls. The results indicate that signaling molecules play an important role in dentin/pulp regeneration. However, further studies are needed to determine a more specific subset combination of molecules to achieve greater efficiency towards the desired tissue engineering applications.

Keywords: cell homing; dentin-pulp complex regeneration; signaling molecules; tissue engineering.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Animals
  • Dental Pulp
  • Dentin*
  • Regeneration
  • Tissue Engineering / methods
  • Vascular Endothelial Growth Factor A*

Substances

  • Vascular Endothelial Growth Factor A