Journal article
A focus on the preclinical development and clinical status of the histone deacetylase inhibitor, romidepsin (depsipeptide, Istodax®)
SJ Harrison, M Bishton, SE Bates, S Grant, RL Piekarz, RW Johnstone, Y Dai, B Lee, ME Araujo, HM Prince
Epigenomics | FUTURE MEDICINE LTD | Published : 2012
DOI: 10.2217/epi.12.52
Abstract
Romidepsin (Istodax®, depsipeptide, FR901228, FK228, NSC 630176) is a cyclic peptide, broad-spectrum, potent histone deacetylase inhibitor, with activity mainly against class I histone deacetylase enzymes. In this article, we give an overview of the putative modes of action, such as effects on gene expression, cell cycle regulation, apoptosis induction, DNA repair, protein acetylation and induction of autophagy. Romidepsin has mainly been developed as a therapy for hematologic malignancies and is approved by the US FDA for the treatment of cutaneous T-cell lymphomas. This report outlines the laboratory and clinical development of the compound as a single agent that has more recently been eva..
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Awarded by National Cancer Institute
Funding Acknowledgements
SJ Harrison and HM Prince have received grant funding and honoraria from Celgene. SE Bates recieves funding via Cooperative Research and Development Agreement between NCI and Celgene. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.