The immunoreceptor NKG2D promotes tumour growth in a model of hepatocellular carcinoma

Nat Commun. 2017 Jan 27:8:13930. doi: 10.1038/ncomms13930.

Abstract

Inflammation is recognized as one of the drivers of cancer. Yet, the individual immune components that possess pro- and anti-tumorigenic functions in individual cancers remain largely unknown. NKG2D is a potent activating immunoreceptor that has emerged as an important player in inflammatory disorders besides its well-established function as tumour suppressor. Here, we provide genetic evidence of an unexpected tumour-promoting effect of NKG2D in a model of inflammation-driven liver cancer. Compared to NKG2D-deficient mice, NKG2D-sufficient mice display accelerated tumour growth associated with, an increased recruitment of memory CD8+T cells to the liver and exacerbated pro-inflammatory milieu. In addition, we show that NKG2D contributes to liver damage and consequent hepatocyte proliferation known to favour tumorigenesis. Thus, the NKG2D/NKG2D-ligand pathway provides an additional mechanism linking chronic inflammation to tumour development in hepatocellular carcinoma. Our findings expose the need to selectively target the types of cancer that could benefit from NKG2D-based immunotherapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents, Immunological / pharmacology
  • Antineoplastic Agents, Immunological / therapeutic use
  • Carcinogenesis / drug effects
  • Carcinogenesis / pathology
  • Carcinoma, Hepatocellular / chemically induced
  • Carcinoma, Hepatocellular / drug therapy
  • Carcinoma, Hepatocellular / immunology
  • Carcinoma, Hepatocellular / pathology*
  • Cell Proliferation / drug effects
  • Diethylnitrosamine / toxicity
  • Disease Progression
  • Hepatocytes / immunology
  • Hepatocytes / pathology
  • Humans
  • Immunotherapy / methods
  • Ligands
  • Liver / cytology
  • Liver / pathology
  • Liver Neoplasms / chemically induced
  • Liver Neoplasms / drug therapy
  • Liver Neoplasms / immunology
  • Liver Neoplasms / pathology*
  • Liver Neoplasms, Experimental / chemically induced
  • Liver Neoplasms, Experimental / drug therapy
  • Liver Neoplasms, Experimental / immunology
  • Liver Neoplasms, Experimental / pathology*
  • Male
  • Mice
  • Mice, Knockout
  • NK Cell Lectin-Like Receptor Subfamily K / genetics
  • NK Cell Lectin-Like Receptor Subfamily K / immunology
  • NK Cell Lectin-Like Receptor Subfamily K / metabolism*
  • T-Lymphocytes, Cytotoxic / drug effects
  • T-Lymphocytes, Cytotoxic / immunology
  • T-Lymphocytes, Cytotoxic / metabolism
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / immunology
  • Tumor Suppressor Proteins / metabolism*

Substances

  • Antineoplastic Agents, Immunological
  • Klrk1 protein, mouse
  • Ligands
  • NK Cell Lectin-Like Receptor Subfamily K
  • Tumor Suppressor Proteins
  • Diethylnitrosamine