Direct potentiation of NK cell cytotoxicity by 8-azaguanine with potential antineoplastic activity

Int Immunopharmacol. 2019 Feb:67:152-159. doi: 10.1016/j.intimp.2018.12.020. Epub 2018 Dec 12.

Abstract

This study identified 8-azaguanine (8-AG) as a novel immunomodulatory drug (IMiD) through a high-throughput screen of the Preswick Chemical Library in a model of human NK cell cytotoxicity against blood cancer cells. 8-AG, originally developed as an antineoplastic agent, significantly increased the cytotoxicity of NK cells and was superior in this activity to previously known IMiDs, such as fluoxetine and amphotericin B, identified from the same library. IFN-γ expression was also slightly increased by 8-AG. Mechanistically, 8-AG increased conjugate formation between NK and target cells and subsequent cytolytic granule polarization, but not calcium mobilization, regulation of activating receptors, or expression of perforin or granzyme B. Thus, the antineoplastic activity of 8-AG should be re-evaluated in light of this novel potentiating effect on NK cells.

Keywords: 8-azaguanine; Cytotoxicity; Immunomodulatory drugs; Library screening; NK cells.

MeSH terms

  • Amphotericin B / therapeutic use
  • Antineoplastic Agents / therapeutic use*
  • Azaguanine / therapeutic use*
  • Cells, Cultured
  • Cytoplasmic Granules / metabolism
  • Cytotoxicity, Immunologic
  • Drug Screening Assays, Antitumor
  • Fluoxetine / therapeutic use
  • Granzymes / metabolism
  • Hematologic Neoplasms / drug therapy*
  • Humans
  • Immunologic Factors / therapeutic use*
  • Killer Cells, Natural / immunology*
  • Lymphocyte Activation
  • Perforin / genetics
  • Perforin / metabolism
  • Small Molecule Libraries

Substances

  • Antineoplastic Agents
  • Immunologic Factors
  • Small Molecule Libraries
  • Fluoxetine
  • Perforin
  • Amphotericin B
  • Granzymes
  • Azaguanine