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The Search for Potent, Small-Molecule HDACIs in Cancer Treatment: A Decade After Vorinostat

Journal

MEDICINAL RESEARCH REVIEWS
Volume 37, Issue 6, Pages 1373-1428

Publisher

WILEY
DOI: 10.1002/med.21437

Keywords

histone deacetylase inhibitors; hydroxamic acids; benzamides; cyclic peptides; epigenetics

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Histone deacetylases (HDACs) play a crucial role in the remodeling of chromatin, and are involved in the epigenetic regulation of gene expression. In the last decade, inhibition of HDACs came out as a target for specific epigenetic changes associated with cancer and other diseases. Until now, more than 20 HDAC inhibitors (HDACIs) have entered clinical studies, and some of them (e.g., vorinostat, romidepsin) have been approved for the treatment of cutaneous T-cell lymphoma. This review provides an overview of current knowledge, progress, and molecular mechanisms of HDACIs, covering a period from 2011 until 2015. (C) 2017 Wiley Periodicals, Inc.

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