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Histone Deacetylase Inhibitors: Overview and Perspectives
Histone deacetylase inhibitors (HDACi) comprise structurally diverse compounds that are a group of targeted anticancer agents. The first of these new HDACi, vorinostat (suberoylanilide hydroxamic acid), has received Food and Drug Administration approval for treating patients with cutaneous T-cell ly...
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Published in: | Molecular cancer research 2007-10, Vol.5 (10), p.981-989 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Histone deacetylase inhibitors (HDACi) comprise structurally diverse compounds that are a group of targeted anticancer agents.
The first of these new HDACi, vorinostat (suberoylanilide hydroxamic acid), has received Food and Drug Administration approval
for treating patients with cutaneous T-cell lymphoma. This review focuses on the activities of the 11 zinc-containing HDACs,
their histone and nonhistone protein substrates, and the different pathways by which HDACi induce transformed cell death.
A hypothesis is presented to explain the relative resistance of normal cells to HDACi-induced cell death. (Mol Cancer Res
2007;5(10):981–9) |
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ISSN: | 1541-7786 1557-3125 |
DOI: | 10.1158/1541-7786.MCR-07-0324 |