Autophagy and immune microenvironment in craniopharyngioma and ameloblastoma

Exp Mol Pathol. 2021 Dec:123:104712. doi: 10.1016/j.yexmp.2021.104712. Epub 2021 Oct 13.

Abstract

Background: Craniopharyngiomas and ameloblastomas show remarkable histologic and molecular similarities. The immune microenvironment of craniopharyngiomas has been recently studied showing interesting findings, while its composition in ameloblastomas is unknown. Similarly, some evidence of autophagic activity, a process of cellular constituents' degradation has been found in ameloblastomas, but no studies exist in craniopharyngiomas. Thus, the aim of the study is to compare factors of the immune microenvironment and the autophagic apparatus between these two tumor types.

Methods: 26 craniopharyngiomas and 14 ameloblastomas were immunohistochemically studied for PD-L1, CD8, CD20, S100, CD163, MECA-79, LC3B and p62.

Results: Craniopharyngiomas showed higher LC3B tumor cell expression, higher CD8+ T cells and higher CD163+ macrophages in comparison to ameloblastomas. LC3B tumor cell expression was associated with overall survival in craniopharyngioma patients and p62 nuclear expression was associated with overall survival in ameloblastoma patients.

Conclusion: This is the first study showing the presence of autophagic markers in craniopharyngiomas and describing the immune microenvironment of ameloblastomas.

Keywords: High endothelial venules; LC3B; Lymphocytes; MECA-79; Macrophages; Odontogenic; PD-L1; p62.

MeSH terms

  • Ameloblastoma / genetics
  • Ameloblastoma / immunology*
  • Ameloblastoma / pathology
  • Antigens, CD / genetics
  • Antigens, CD20 / genetics
  • Antigens, Differentiation, Myelomonocytic / genetics
  • Antigens, Surface / genetics
  • Autophagy / immunology
  • B7-H1 Antigen / genetics
  • CD8 Antigens / genetics
  • CD8-Positive T-Lymphocytes / immunology
  • Craniopharyngioma / genetics
  • Craniopharyngioma / immunology*
  • Craniopharyngioma / pathology
  • Gene Expression Regulation, Neoplastic / immunology
  • Humans
  • Macrophages / immunology
  • Membrane Proteins / genetics
  • Microtubule-Associated Proteins / genetics
  • Pituitary Neoplasms / genetics
  • Pituitary Neoplasms / immunology*
  • Pituitary Neoplasms / pathology
  • RNA-Binding Proteins / genetics
  • Receptors, Cell Surface / genetics
  • S100 Proteins / genetics
  • Tumor Microenvironment / genetics
  • Tumor Microenvironment / immunology*

Substances

  • Antigens, CD
  • Antigens, CD20
  • Antigens, Differentiation, Myelomonocytic
  • Antigens, Surface
  • B7-H1 Antigen
  • CD163 antigen
  • CD274 protein, human
  • CD8 Antigens
  • L-selectin counter-receptors
  • MAP1LC3B protein, human
  • Membrane Proteins
  • Microtubule-Associated Proteins
  • P62 protein, human
  • RNA-Binding Proteins
  • Receptors, Cell Surface
  • S100 Proteins