| Literature DB >> 25017212 |
Seth A Brodie1, Johann C Brandes.
Abstract
Valproic acid is an inhibitor of class I histone deacetylases. Epigenetic therapies in cancer have been focus of a keen interest and histone deacetylase inhibitors, in particular, have been approved for certain types of hematologic malignancies. Valproic acid is an attractive candidate for cancer therapy due to its mechanism of action, its low cost and generally good clinical tolerability. In the following editorial, we will review its role as monotherapy for cancer, its place in combination epigenetic therapy, and its role as chemosensitizer, and cancer preventative agent.Entities:
Keywords: AML; HDAC; MDS; cancer prevention; methylation; valproic acid
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Year: 2014 PMID: 25017212 PMCID: PMC4579528 DOI: 10.1586/14737140.2014.940329
Source DB: PubMed Journal: Expert Rev Anticancer Ther ISSN: 1473-7140 Impact factor: 4.512