Targeting SALL4 by entinostat in lung cancer

Oncotarget. 2016 Nov 15;7(46):75425-75440. doi: 10.18632/oncotarget.12251.

Abstract

The overall survival of lung cancer patients remains dismal despite the availability of targeted therapies. Oncofetal protein SALL4 is a novel cancer target. We herein report that SALL4 was aberrantly expressed in a subset of lung cancer patients with poor survival. SALL4 silencing by RNA interference or SALL4 peptide inhibitor treatment led to impaired lung cancer cell growth. Expression profiling of SALL4-knockdown cells demonstrated that both the EGFR and IGF1R signaling pathways were affected. Connectivity Map analysis revealed the HDAC inhibitor entinostat as a potential drug in treating SALL4-expressing cancers, and this was confirmed in 17 lung cancer cell lines. In summary, we report for the first time that entinostat can target SALL4-positive lung cancer. This lays the foundation for future clinical studies evaluating the therapeutic efficacy of entinostat in SALL4-positive lung cancer patients.

Keywords: HDAC inhibitor; SALL4; entinostat; lung cancer.

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology*
  • Benzamides / pharmacology*
  • Cell Line, Tumor
  • Cell Survival / genetics
  • Disease Models, Animal
  • Gene Expression
  • Histone Deacetylase Inhibitors / pharmacology*
  • Humans
  • Lung Neoplasms
  • Mice
  • Pyridines / pharmacology*
  • RNA Interference
  • RNA, Small Interfering / genetics
  • Transcription Factors / antagonists & inhibitors*
  • Xenograft Model Antitumor Assays

Substances

  • Antineoplastic Agents
  • Benzamides
  • Histone Deacetylase Inhibitors
  • Pyridines
  • RNA, Small Interfering
  • SALL4 protein, human
  • Transcription Factors
  • entinostat