miR-30c-1* promotes natural killer cell cytotoxicity against human hepatoma cells by targeting the transcription factor HMBOX1

Cancer Sci. 2012 Apr;103(4):645-52. doi: 10.1111/j.1349-7006.2012.02207.x. Epub 2012 Feb 13.

Abstract

Natural killer (NK) cells play a critical role in antitumor immunity, and the activation of NK cells is regulated by a series of NK cell receptors. Here, we show that crosslinking CD226, an important NK cell receptor, with the anti-CD226 mAb LeoA1 on NKL cells, regulated the expression of several microRNA and transmembrane tumor necrosis factor-α. Among them, miR-30c-1(*) was noticed because overexpression of miR-30c-1(*) triggered upregulation of transmembrane tumor necrosis factor-α expression and enhanced NK cell cytotoxicity against hepatoma cell lines SMMC-7721 and HepG2. Furthermore, we proved that the inhibitory transcription factor HMBOX1, which depressed the activation of NK cells, was the direct target gene of miR-30c-1(*). In conclusion, our results revealed a novel regulatory mechanism: miR-30c-1(*) promoted NK cell cytotoxicity against hepatoma cells by targeting HMBOX1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Differentiation, T-Lymphocyte
  • Carcinoma, Hepatocellular / immunology*
  • Cell Line, Tumor
  • Cytotoxicity, Immunologic
  • Female
  • Homeodomain Proteins / antagonists & inhibitors*
  • Humans
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism
  • Liver Neoplasms / immunology*
  • Mice
  • MicroRNAs / physiology*
  • T Lineage-Specific Activation Antigen 1
  • Tumor Necrosis Factor-alpha / biosynthesis*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antigens, Differentiation, T-Lymphocyte
  • T Lineage-Specific Activation Antigen 1
  • HMBOX1 protein, human
  • Homeodomain Proteins
  • MIRN30b microRNA, human
  • MicroRNAs
  • Tumor Necrosis Factor-alpha