Podoplanin Expression Independently and Jointly with Oral Epithelial Dysplasia Grade Acts as a Potential Biomarker of Malignant Transformation in Oral Leukoplakia

Biomolecules. 2022 Apr 19;12(5):606. doi: 10.3390/biom12050606.

Abstract

Our aim was to evaluate the expression of biomarkers, CD44v6, CD147, EGFR, p53, p63, p73, p16, and podoplanin in oral leukoplakias (OL) and to assess their potential for prediction of malignant transformation (MT). We analyzed the expression of CD44v6, CD147, EGFR, p53, p63, p73, p16, and podoplanin by immunohistochemistry in 52 OL, comprised of 41 low-grade (LG) dysplasia and 11 high-grade (HG) cases. Twelve healthy normal tissues (NT) were also included. Univariate and multivariate analysis were performed to evaluate any association with MT. Variable expression among the studied markers was observed, with a significant increase of high expression from NT to LG and HG cases in CD44v6 (p = 0.002), P53 (p = 0.002), P73 (p = 0.043), and podoplanin (p < 0.001). In multivariate analysis, cases with high podoplanin score showed a significant increased risk of MT (HR of 10.148 (95% CI of 1.503−68.532; p = 0.017). Furthermore, podoplanin combined with binary dysplasia grade obtained a HR of 10.238 (95% CI of 2.06−50.889; p = 0.004). To conclude, CD44v6, p53, p73, and podoplanin showed an increasing expression along the natural history of oral carcinogenesis. Podoplanin expression independently or combined with dysplasia grade could be useful predictive markers of MT in OL.

Keywords: CD147; CD44v6; EGFR; dysplasia; malignant transformation; oral leukoplakia; p16; p53; podoplanin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / metabolism
  • Cell Transformation, Neoplastic / metabolism
  • ErbB Receptors / metabolism
  • Humans
  • Hyperplasia
  • Leukoplakia, Oral / metabolism
  • Leukoplakia, Oral / pathology
  • Membrane Glycoproteins* / genetics
  • Membrane Glycoproteins* / metabolism
  • Transcription Factors / metabolism
  • Tumor Suppressor Protein p53* / metabolism

Substances

  • Biomarkers
  • Membrane Glycoproteins
  • Transcription Factors
  • Tumor Suppressor Protein p53
  • ErbB Receptors