NKG2D (Natural Killer Group 2, Member D) ligand expression and ameloblastoma recurrence: a retrospective immunohistological pilot study

BMC Oral Health. 2024 Sep 17;24(1):1102. doi: 10.1186/s12903-024-04873-8.

Abstract

Background/purpose: This retrospective immunohistological pilot study aimed to investigate the influence of natural killer group 2, member D (NKG2D) ligand expression on ameloblastoma recurrence after surgical resection. It also aimed to elucidate additional clinical factors that could serve as predictors of ameloblastoma recurrence.

Materials and methods: This study included 96 patients who were histologically diagnosed with ameloblastoma after surgical resection. The expression of NKG2D ligands, including UL16-binding proteins (ULBPs) 1-3 and major histocompatibility complex class I chain-related molecule (MIC) A/B, was evaluated in formalin-fixed paraffin-embedded tumor tissues via immunohistochemistry assays. Furthermore, the patients' electronic medical records were reviewed. Multivariate Cox regression analysis was conducted, and data were expressed as adjusted hazard ratios [HRs] with 95% confidence intervals [95% CIs].

Results: Multivariate analysis revealed that recurrent tumors (ref.: primary; adjusted HR [95% CI]: 2.780 [1.136, 6.803], p = 0.025) and positive MICA/B expression (ref.: negative; adjusted HR [95% CI]: 0.223 [0.050, 0.989], p = 0.048) independently affected recurrence-free survival in ameloblastoma.

Conclusion: This study identified recurrent cases and loss of MICA/B expression as independent predictors of early ameloblastoma recurrence following surgical resection. The findings suggest that decreased MICA/B expression might undermine NKG2D-mediated tumor immunosurveillance, thereby influencing early recurrence.

Keywords: Ameloblastoma; Cytotoxicity, immunologic; Killer cells, natural; Odontogenic tumors.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Ameloblastoma* / metabolism
  • Ameloblastoma* / pathology
  • Ameloblastoma* / surgery
  • Female
  • Humans
  • Immunohistochemistry
  • Jaw Neoplasms / metabolism
  • Jaw Neoplasms / pathology
  • Jaw Neoplasms / surgery
  • Male
  • Middle Aged
  • NK Cell Lectin-Like Receptor Subfamily K / metabolism
  • Neoplasm Recurrence, Local* / pathology
  • Pilot Projects
  • Retrospective Studies
  • Young Adult

Substances

  • NK Cell Lectin-Like Receptor Subfamily K
  • KLRK1 protein, human