Podoplanin expression as a predictive marker of dysplasia in oral leukoplakia

J Craniomaxillofac Surg. 2018 May;46(5):759-764. doi: 10.1016/j.jcms.2018.02.016. Epub 2018 Mar 9.

Abstract

Purpose: Recent studies have emphasized the role of podoplanin in oral lesions at risk of malignant transformation. We investigated a group of oral leukoplakias (OLs) to determine a possible relation between altered podoplanin expression and dysplasia, and to compare the results with those obtained by other, widely used biomarkers.

Materials and methods: The population consisted of 40 consecutive patients with a clinical and histological diagnosis of OL. Thirty-two OLs did not show dysplasia, whereas eight lesions presented with dysplasia. Immunohistochemical expression of podoplanin, p53 and Ki67 was analyzed in all samples.

Results: All three biomarkers were positive in seven of eight dysplastic OLs. Among the 32 OLs without dysplasia, Ki67 and p53 showed positive values in 21 and 10 samples respectively, whereas podoplanin was positive in only one case. Multiple logistic regression showed that podoplanin was the most powerful variable (Chi square 9.77; p < .01) statistically related to the presence of dysplasia. In addition, podoplanin showed a higher specificity value (96.87%) than Ki67 (34.37%) and p53 (68.75%).

Conclusion: Podoplanin seems to be a reliable means of discriminating lesions with epithelial dysplasia and could be introduced in routine practice as a marker to discriminate OLs at risk of developing cancer.

Keywords: Dysplasia; Ki67; Oral leukoplakia; Podoplanin; p53.

MeSH terms

  • Biomarkers / metabolism
  • Cell Transformation, Neoplastic / metabolism
  • Cell Transformation, Neoplastic / pathology
  • Female
  • Humans
  • Ki-67 Antigen / metabolism
  • Leukoplakia, Oral / diagnosis
  • Leukoplakia, Oral / metabolism*
  • Leukoplakia, Oral / pathology
  • Male
  • Membrane Glycoproteins / metabolism*
  • Middle Aged
  • Mouth / metabolism
  • Mouth / pathology
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Biomarkers
  • Ki-67 Antigen
  • Membrane Glycoproteins
  • PDPN protein, human
  • Tumor Suppressor Protein p53