Histone deacetylase inhibitors in the treatment of cancer: overview and perspectives

Future Med Chem. 2012 Jul;4(11):1439-60. doi: 10.4155/fmc.12.80.

Abstract

Histone deacetylase inhibitors (HDACis) are one of the last frontiers in pharmaceutical research. Several classes of HDACi have been identified. Although more than 20 HDACi are under preclinical and clinical investigation as single agents and in combination therapies against different cancers, just two of them were approved by the US FDA: Zolinza(®) and Istodax(®), both licensed for the treatment of cutaneous T-cell lymphoma, the latter also of peripheral T-cell lymphoma. Since HDAC enzymes act by forming multiprotein complexes (clusters), containing cofactors, the main problem in designing new HDACi is that the inhibition activity evaluated on isolated enzyme isoforms does not match the in vivo outcomes. In the coming years, the research will be oriented toward a better understanding of the functioning of these protein complexes as well as the development of new screening assays, with the final goal to obtain new drug candidates for the treatment of cancer.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Apoptosis / drug effects
  • Depsipeptides / pharmacology
  • Depsipeptides / therapeutic use
  • Drug Design
  • Drug Therapy, Combination
  • Histone Deacetylase Inhibitors / pharmacology
  • Histone Deacetylase Inhibitors / therapeutic use*
  • Histone Deacetylases / chemistry*
  • Histone Deacetylases / metabolism
  • Humans
  • Hydroxamic Acids / pharmacology
  • Hydroxamic Acids / therapeutic use
  • Lymphoma, T-Cell, Cutaneous / drug therapy
  • Neoplasms / drug therapy*
  • Neoplasms / enzymology
  • Protein Isoforms / antagonists & inhibitors
  • Protein Isoforms / metabolism
  • Vorinostat

Substances

  • Antineoplastic Agents
  • Depsipeptides
  • Histone Deacetylase Inhibitors
  • Hydroxamic Acids
  • Protein Isoforms
  • Vorinostat
  • romidepsin
  • Histone Deacetylases