Histone Deacetylase Inhibitors Enhance Cell Killing and Block Interferon-Beta Synthesis Elicited by Infection with an Oncolytic Parainfluenza Virus

Viruses. 2019 May 10;11(5):431. doi: 10.3390/v11050431.

Abstract

Previous results have shown that infection with the cytoplasmic-replicating parainfluenza virus 5 mutant P/V-CPI- sensitizes cells to DNA damaging agents, resulting in the enhanced killing of airway cancer cells. Here, we have tested the hypothesis that histone deacetylase (HDAC) inhibitors can also act with P/V-CPI- infection to enhance cancer cell killing. Using human small cell lung cancer and laryngeal cancer cell lines, 10 HDAC inhibitors were tested for their effect on viability of P/V-CPI- infected cells. HDAC inhibitors such as scriptaid enhanced caspase-3/7, -8 and -9 activity induced by P/V-CPI- and overall cell toxicity. Scriptaid-mediated enhanced killing was eliminated in lung cancer cells that were engineered to express a protein which sequesters double stranded RNA. Scriptaid also enhanced cancer cell killing by two other negative strand RNA viruses - the La Crosse virus and vesicular stomatitis virus. Scriptaid treatment enhanced the spread of the P/V-CPI- virus through a population of cancer cells, and suppressed interferon-beta induction through blocking phosphorylation and nuclear translocation of Interferon Regulatory Factor 3 (IRF-3). Taken together, these data support a role for combinations of a cytoplasmic-replicating RNA virus such as the P/V-CPI- mutant along with chemotherapeutic agents.

Keywords: histone deacetylase inhibitors; oncolytic virus; parainfluenza virus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Caspases / genetics
  • Caspases / metabolism
  • Cell Line, Tumor
  • Histone Deacetylase Inhibitors / pharmacology*
  • Humans
  • Hydroxylamines / pharmacology
  • Interferon Regulatory Factor-3 / genetics
  • Interferon Regulatory Factor-3 / metabolism
  • Interferon-beta / biosynthesis*
  • Neoplasms / genetics
  • Neoplasms / metabolism*
  • Neoplasms / therapy
  • Neoplasms / virology
  • Oncolytic Viruses / genetics
  • Oncolytic Viruses / physiology*
  • Parainfluenza Virus 5 / genetics
  • Parainfluenza Virus 5 / physiology*
  • Quinolines / pharmacology

Substances

  • Histone Deacetylase Inhibitors
  • Hydroxylamines
  • IRF3 protein, human
  • Interferon Regulatory Factor-3
  • Quinolines
  • scriptaid
  • Interferon-beta
  • Caspases