Journal article
Antimalarial activity of the anticancer histone deacetylase inhibitor SB939
SDM Sumanadasa, CD Goodman, AJ Lucke, T Skinner-Adams, I Saham, A Haque, TA Do, GI McFadden, DP Fairlie, KT Andrews
Antimicrobial Agents and Chemotherapy | Published : 2012
DOI: 10.1128/AAC.00030-12
Abstract
Histone deacetylase (HDAC) enzymes posttranslationally modify lysines on histone and nonhistone proteins and play crucial roles in epigenetic regulation and other important cellular processes. HDAC inhibitors (e.g., suberoylanilide hydroxamic acid [SAHA; also known as vorinostat]) are used clinically to treat some cancers and are under investigation for use against many other diseases. Development of new HDAC inhibitors for noncancer indications has the potential to be accelerated by piggy-backing onto cancer studies, as several HDAC inhibitors have undergone or are undergoing clinical trials. One such compound, SB939, is a new orally active hydroxamate-based HDAC inhibitor with an improved ..
View full abstractRelated Projects (2)
Grants
Awarded by Australian Research Council
Awarded by Australian National Health and Medical Research Council
Funding Acknowledgements
We thank the Australian Research Council (grant FF0668705 to G.I.M., grant FF0668733 to D.P.F., and grant FT0991213 to K.T.A.) and the Australian National Health and Medical Research Council (grant 569735 to D.P.F. and grant 637406 to G.I.M.) for research and fellowship support.