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New Clinical Developments in Histone Deacetylase Inhibitors for Epigenetic Therapy of Cancer

Overview
Journal J Hematol Oncol
Publisher Biomed Central
Specialties Hematology
Oncology
Date 2009 Jun 3
PMID 19486511
Citations 36
Authors
Affiliations
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Abstract

DNA methylation and histone acetylation are two well known epigenetic chromatin modifications. Epigenetic agents leading to DNA hypomethylation and histone hyperacetylation have been approved for treatment of hematological disorders. The first histone deacetylase inhibitor, vorinostat, has been licensed for cutaneous T cell lymphoma treatment. More than 11 new epigenetic agents are in various stages of clinical development for therapy of multiple cancer types. In this review we summarize novel histone deacetylase inhibitors and new regimens from clinical trials for epigenetic therapy of cancer.

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References
1.
Blumenschein Jr G, Kies M, Papadimitrakopoulou V, Lu C, Kumar A, Ricker J . Phase II trial of the histone deacetylase inhibitor vorinostat (Zolinza, suberoylanilide hydroxamic acid, SAHA) in patients with recurrent and/or metastatic head and neck cancer. Invest New Drugs. 2007; 26(1):81-7. DOI: 10.1007/s10637-007-9075-2. View

2.
Marks P . Discovery and development of SAHA as an anticancer agent. Oncogene. 2007; 26(9):1351-6. DOI: 10.1038/sj.onc.1210204. View

3.
Carducci M, Gilbert J, Bowling M, Noe D, Eisenberger M, Sinibaldi V . A Phase I clinical and pharmacological evaluation of sodium phenylbutyrate on an 120-h infusion schedule. Clin Cancer Res. 2001; 7(10):3047-55. View

4.
Bali P, Pranpat M, Bradner J, Balasis M, Fiskus W, Guo F . Inhibition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: a novel basis for antileukemia activity of histone deacetylase inhibitors. J Biol Chem. 2005; 280(29):26729-34. DOI: 10.1074/jbc.C500186200. View

5.
Kelly W, Marks P . Drug insight: Histone deacetylase inhibitors--development of the new targeted anticancer agent suberoylanilide hydroxamic acid. Nat Clin Pract Oncol. 2005; 2(3):150-7. DOI: 10.1038/ncponc0106. View