Transcriptional modulation using HDACi depsipeptide promotes immune cell-mediated tumor destruction of murine B16 melanoma

J Invest Dermatol. 2008 Jun;128(6):1506-16. doi: 10.1038/sj.jid.5701216. Epub 2008 Jan 10.

Abstract

With melanoma, as with many other malignancies, aberrant transcriptional repression is a hallmark of refractory cancer. To restore gene expression, use of a histone deacetylase inhibitor (HDACi) is expected to be effective. Our recent DNA micro-array analysis showed that the HDACi depsipeptide (FK228) significantly enhances gp100 antigen expression. Herein, we demonstrate that depsipeptide promotes tumor-specific T-cell-mediated killing of B16/F10 murine melanoma cells. First, by a quantitative assay of caspase-3/7 activity, a sublethal dose of depsipeptide was determined (ED50: 5 nM), in which p21(Waf1/Cip1) and Fas were sufficiently evoked concomitantly with histone H3 acetylation. Second, the sublethal dose of depsipeptide treatment with either a recombinant Fas ligand or tumor-specific T cells synergistically enhanced apoptotic cell death in B16/F10 cells in vitro. Furthermore, we found that depsipeptide increased levels of perforin in T cells. Finally, in vivo metastatic growth of B16/F10 in the lung was significantly inhibited by a combination of depsipeptide treatment and immune cell adoptive transfer from immunized mice using irradiated B16 cells and gp100-specific (Pmel-1) TCR transgenic mice (P<0.05, vs cell transfer alone). Consequently, employment of a transcriptional modulation strategy using HDACis might prove to be a useful pretreatment for human melanoma immunotherapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibiotics, Antineoplastic / pharmacology
  • Caspase 3 / metabolism
  • Caspase 7 / metabolism
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism
  • Depsipeptides / pharmacology
  • Gene Expression Regulation, Neoplastic*
  • Histone Deacetylases / metabolism
  • Melanoma / pathology
  • Melanoma, Experimental
  • Mice
  • Mice, Transgenic
  • Oligonucleotide Array Sequence Analysis
  • Transcription, Genetic*
  • fas Receptor / metabolism

Substances

  • Antibiotics, Antineoplastic
  • Cdkn1a protein, mouse
  • Cyclin-Dependent Kinase Inhibitor p21
  • Depsipeptides
  • fas Receptor
  • romidepsin
  • Caspase 3
  • Caspase 7
  • Histone Deacetylases