Journal of Oral and Maxillofacial Surgery
Volume 66, Issue 10 , Pages 2004-2011, October 2008

Determination of Potential Cellular Proliferation in the Odontogenic Epithelia of the Dental Follicle of the Asymptomatic Impacted Third Molars

  • Fatih Cabbar, DDS, MSc

      Affiliations

    • Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, University of Yeditepe, Istanbul, Turkey
    • Corresponding Author InformationAddress correspondence and reprint requests to Dr Cabbar: Yeditepe University, Faculty of Dentistry, Department of Oral and Maxillofacial Surgery, Bagdat Cad. No:238 Goztepe, 34728 Istanbul, Turkey
  • ,
  • Nurhan Güler, DDS, PhD

      Affiliations

    • Associate Professor, Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, University of Yeditepe, Istanbul, Turkey
  • ,
  • Nil Comunoğlu, MD

      Affiliations

    • Associate Professor, Department of Pathology, Faculty of Medicine, University of Yeditepe, Istanbul, Turkey
  • ,
  • Kemal Şençift, DDS, PhD

      Affiliations

    • Professor, Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, University of Yeditepe, Istanbul, Turkey
  • ,
  • Sedat Çöloğlu, MD

      Affiliations

    • Professor, Department of Pathology, Faculty of Medicine, University of Yeditepe, Istanbul, Turkey

Purpose

The aim of this study is to determine the proliferative potentials of dental follicles (DF) of radiographically asymptomatic impacted third molar teeth by using Ki-67 and mini-chromosome maintenance protein 2 (MCM-2) proliferation markers, and to discuss whether there is any necessity for the removal of all impacted third molars by detecting the potential of the developing cysts and tumors of its DF.

Materials and Methods

This study involved 59 DF of 54 patients referred for clinically and radiographically asymptomatic lower impacted third molars. Thirteen healthy gingiva tissues obtained during the impacted third molar operation in 13 patients served as a control group. DF widths on periapical radiographs below 2.5 mm were included in the study. The epithelial and mesenchymal components of DF were examined histologically. All specimens were stained with periodic acid Schiff, Alcian blue, and mucin for the evaluation of mucous cell prosoplasia. Epithelial cell proliferation was determined by using immunohistochemical labeling.

Results

The histologic examinations showed 11.9% mucous cell prosoplasia, 55.9% squamous metaplasia, 15.3% glandular epithelium, and 33.9% inflammation. Ki-67 expression was found to have higher values than MCM-2 expression in controls 6.15 (3.18) and 10.53 (5.77) and in DF 4.46 (1.39) and 5.89 (2.89), respectively. The expression of both proliferation markers in the basal epithelial cells, mucous, and squamous epithelium and inflammatory cells were statistically significant (P < .01).

Conclusion

The results of this study indicate that the odontogenic epithelium in DF of asymptomatic impacted third molars might be actively proliferating and may be an indicator for the differentiation potential of DF. It would also seem that the inflammation observed in the mesenchymal components of DF up-regulate the cell turnover of odontogenic epithelium and lead to proliferation. Based on these observations, we support prophylactic removal of impacted third molars.

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 This study was supported by TUBITAK (grant no. 106S236 [SBAG-HD-159]).

PII: S0278-2391(08)01053-7

doi:10.1016/j.joms.2008.06.011

Journal of Oral and Maxillofacial Surgery
Volume 66, Issue 10 , Pages 2004-2011, October 2008