HDAC8 and STAT3 repress BMF gene activity in colon cancer cells

Cell Death Dis. 2014 Oct 16;5(10):e1476. doi: 10.1038/cddis.2014.422.

Abstract

Histone deacetylase (HDAC) inhibitors are undergoing clinical trials as anticancer agents, but some exhibit resistance mechanisms linked to anti-apoptotic Bcl-2 functions, such as BH3-only protein silencing. HDAC inhibitors that reactivate BH3-only family members might offer an improved therapeutic approach. We show here that a novel seleno-α-keto acid triggers global histone acetylation in human colon cancer cells and activates apoptosis in a p21-independent manner. Profiling of multiple survival factors identified a critical role for the BH3-only member Bcl-2-modifying factor (Bmf). On the corresponding BMF gene promoter, loss of HDAC8 was associated with signal transducer and activator of transcription 3 (STAT3)/specificity protein 3 (Sp3) transcription factor exchange and recruitment of p300. Treatment with a p300 inhibitor or transient overexpression of exogenous HDAC8 interfered with BMF induction, whereas RNAi-mediated silencing of STAT3 activated the target gene. This is the first report to identify a direct target gene of HDAC8 repression, namely, BMF. Interestingly, the repressive role of HDAC8 could be uncoupled from HDAC1 to trigger Bmf-mediated apoptosis. These findings have implications for the development of HDAC8-selective inhibitors as therapeutic agents, beyond the reported involvement of HDAC8 in childhood malignancy.

Publication types

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

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics*
  • Apoptosis / drug effects
  • Colonic Neoplasms / enzymology
  • Colonic Neoplasms / genetics*
  • Colonic Neoplasms / pathology
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism
  • E1A-Associated p300 Protein / metabolism
  • HCT116 Cells
  • Histone Deacetylases / metabolism*
  • Humans
  • Models, Biological
  • Pyruvates / pharmacology
  • Repressor Proteins / metabolism*
  • STAT3 Transcription Factor / metabolism*
  • Transcription, Genetic / drug effects

Substances

  • Adaptor Proteins, Signal Transducing
  • BMF protein, human
  • Cyclin-Dependent Kinase Inhibitor p21
  • Pyruvates
  • Repressor Proteins
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • E1A-Associated p300 Protein
  • EP300 protein, human
  • HDAC8 protein, human
  • Histone Deacetylases