CD133 Role in Oral Carcinogenesis

Asian Pac J Cancer Prev. 2020 Sep 1;21(9):2501-2506. doi: 10.31557/APJCP.2020.21.9.2501.

Abstract

Objective: to investigate CD133 immunoexpression, cancer stem cells marker, in oral epithelial dysplasias (OEDs) and oral squamous cells carcinomas (OSCCs) and understandits possible involvement in the malignant transformation process of these lesions and to better elucidate their biological behavior.

Material and methods: Tissue samples of 15 cases of OSCCs and 15 OEDs were subjected to CD133 antibody immunohistochemistry reactions. The analysis used quantitative parameters (number of immunostained cells regardless of immunostaining sublocations).

Results: All samples of OSCCs and OEDs showed positive immunostaining, with no significant difference between these groups (p = 0.283). We did not observe statistical difference between the degree of dysplasia and the amount of CD133+ cells (p = 0.899). CD133 immunoexpression showed no association with the OEDs and OSCCs sites. It was observed that nuclear and cytoplasmic immunostaining was more evident with the progression of the malignant process.

Conclusion: It is suggested that the CD133 cellular localization together with the histopathological criteria of OEDs classification can contribute to provide more concrete indications about the oral carcinogenesis process.

Keywords: CD133; oral carcinogenesis; oral squamous cells carcinoma; premalignant lesions; stem cells.

MeSH terms

  • AC133 Antigen / metabolism*
  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / metabolism*
  • Carcinoma, Squamous Cell / metabolism
  • Carcinoma, Squamous Cell / pathology*
  • Female
  • Focal Epithelial Hyperplasia / metabolism
  • Focal Epithelial Hyperplasia / pathology*
  • Follow-Up Studies
  • Humans
  • Male
  • Middle Aged
  • Mouth Neoplasms / metabolism
  • Mouth Neoplasms / pathology*
  • Precancerous Conditions / metabolism
  • Precancerous Conditions / pathology*
  • Prognosis

Substances

  • AC133 Antigen
  • Biomarkers, Tumor
  • PROM1 protein, human