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• W2079620992 abstract "Post-translational modifications of histone and non-histone proteins by acetylation are known to play a key role in tumourigenesis. Pharmacological manipulation of acetylation has been possible with the identification of small molecule inhibitors of histone deacetylases (HDAC), the enzymes responsible for deacetylating lysine residues. An explosion of drug discovery efforts in recent years has led to the development of an extensive group of HDAC inhibitors, many of which have been shown pre-clinically to have potent anti-tumour activity. Clinical trials using these agents are now underway, with Vorinostat (suberoylanilide hydroxamic acid) having been approved by the FDA for treating cutaneous T-cell lymphoma (CTCL) in patients with progressive, persistent or recurrent disease. This review discusses how biomarkers are being identified and used to expand our knowledge of the mechanisms by which HDAC inhibitors exhibit their anti-cancer effects. In the longer term, biomarkers will provide a means towards achieving patient stratification in tumour types that will respond favourably to HDAC inhibitors." @default.
• W2079620992 created "2016-06-24" @default.
• W2079620992 creator A5001022039 @default.
• W2079620992 creator A5045302508 @default.
• W2079620992 date "2009-08-01" @default.
• W2079620992 modified "2023-10-13" @default.
• W2079620992 title "Biomarkers for predicting clinical responses to HDAC inhibitors" @default.
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• W2079620992 doi "https://doi.org/10.1016/j.canlet.2009.03.016" @default.
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