Does a polarization state exist for mast cells in cancer?

Med Hypotheses. 2019 Oct:131:109281. doi: 10.1016/j.mehy.2019.109281. Epub 2019 Jun 13.

Abstract

The data of literature are discordant about the role of mast cells in different types of neoplasms. In this paper the authors propose the hypothesis that tumor-associated mast cells may switch to different polarization states, conditioning the immunogenic capacities of the different neoplasms. Anti-inflammatory polarized mast cells should express cytokines such as interleukin-10 (IL-10) and then mast cells number should be inversely related to the intensity of inflammatory infiltrate. On the contrary, when mast cells do not express anti-inflammatory cytokines their number should be directly related to the intensity of the inflammatory infiltrate. In this paper we briefly argue around feasible approaches, based on the retrospective studies of tumor tissue samples from neoplasms considered "immunologically hot" and neoplasms considered "immunologically cold", through immunohistochemistry and immunofluorescence techniques (confocal microscopy). The establishment of the actual existence of a polarization interchange of mast cells, could lead to a new vision in prognostic terms, useful to contrive new approaches in immunotherapy of tumors.

Keywords: Cancer; Innate immunity; Macrophage polarization; Mast cells.

MeSH terms

  • Antigens, CD / analysis
  • Antigens, Differentiation, Myelomonocytic / analysis
  • Antigens, Neoplasm / analysis
  • Cell Count
  • Cytokines / biosynthesis*
  • Gene Expression Regulation, Neoplastic / immunology
  • Humans
  • Immunochemistry
  • Inflammation
  • Lymphocytes, Tumor-Infiltrating / chemistry
  • Macrophages / chemistry
  • Mast Cells / immunology*
  • Mast Cells / metabolism
  • Mast Cells / ultrastructure
  • Microscopy, Confocal
  • Models, Immunological*
  • Neoplasms / chemistry
  • Neoplasms / immunology*
  • Neoplasms / ultrastructure
  • Paraffin Embedding
  • Proto-Oncogene Proteins c-kit / analysis
  • Receptors, Cell Surface / analysis
  • Research Design
  • Retrospective Studies

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Antigens, Neoplasm
  • CD163 antigen
  • CD68 antigen, human
  • Cytokines
  • Receptors, Cell Surface
  • KIT protein, human
  • Proto-Oncogene Proteins c-kit