Targeting histone deacetylase and NFκB signaling as a novel therapy for Mucoepidermoid Carcinomas

Sci Rep. 2018 Feb 1;8(1):2065. doi: 10.1038/s41598-018-20345-w.

Abstract

Malignancies from the salivary glands are rare and represent 11% of all cancers from the oropharyngeal anatomical area. Mucoepidermoid Carcinomas (MEC) is the most common malignancy from the salivary glands. Low survival rates of high-grade Mucoepidermoid Carcinomas (MEC) are particularly associated with the presence of positive lymph nodes, extracapsular lymph node spread, and perineural invasion. Most recently, the presence of cancer stem cells (CSC), and the activation of the NFκB signaling pathway have been suggested as cues for an acquired resistance phenotype. We have previously shown that NFκB signaling is very active in MEC tumors. Herein, we explore the efficacy of NFκB inhibition in combination with class I and II HDAC inhibitor to deplete the population of CSC and to destroy MEC tumor cells. Our finding suggests that disruption of NFκB signaling along with the administration of HDAC inhibitors constitute an effective strategy to manage MEC tumors.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Carcinoma, Mucoepidermoid / metabolism*
  • Cell Line, Tumor
  • Emetine / pharmacology
  • Histone Deacetylase Inhibitors / pharmacology*
  • Humans
  • NF-kappa B / antagonists & inhibitors*
  • NF-kappa B / metabolism
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / metabolism
  • Protein Synthesis Inhibitors / pharmacology*
  • Salivary Gland Neoplasms / metabolism*
  • Vorinostat / pharmacology

Substances

  • Antineoplastic Agents
  • Histone Deacetylase Inhibitors
  • NF-kappa B
  • Protein Synthesis Inhibitors
  • Vorinostat
  • Emetine