Histone deacetylase inhibitors: latest developments, trends and prospects

Oscar Moradei1, Christiane R Maroun, Isabelle Paquin

  • 1MethylGene Inc., 7220 Frederick-Banting, Montréal, Québec H4S 2A1, Canada.

Current Medicinal Chemistry. Anti-Cancer Agents
|September 24, 2005
PubMed

Insights

Histone deacetylase (HDAC) inhibitors are promising anti-cancer drugs. Research is rapidly advancing, with numerous new inhibitors and patents emerging, highlighting their therapeutic potential.

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Oncology

Background:

  • Histone deacetylases (HDACs) and histone acetyltransferases (HATs) regulate protein acetylation.
  • Imbalances in acetylation are linked to human cancers.
  • HDAC inhibition is a developing anti-cancer therapeutic strategy.

Purpose of the Study:

  • To review recent advancements in the design and synthesis of HDAC inhibitors.
  • To highlight novel HDAC inhibitors with potential as anti-cancer agents.

Main Methods:

  • Literature review of research papers and patent applications.
  • Analysis of different structural classes of HDAC inhibitors.

Main Results:

  • Significant research activity from over 30 academic and industrial groups.
  • Disclosure of numerous new HDAC inhibitors in diverse structural classes.
  • Identification of potential anti-cancer drug candidates.

Conclusions:

  • The field of HDAC inhibitors is rapidly evolving.
  • Continued research into novel HDAC inhibitors holds promise for cancer therapy.

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