Literature DB >> 22491302

Clinical development of histone deacetylase inhibitor romidepsin.

P Guan1, H Fang.   

Abstract

Histone deactylase inhibitors have emerged as a promising epigenetic therapy for neoplasic indications. The US Food and Drug Administration granted approval to romidepsin for treatment of cutaneous T cell lymphoma (CTCL) in 2009. Phase I/II trials of romidepsin as monotherapy or hybird therapy have demonstrated substantial efficacy profoundly in CTCL and peripheral T-cell lymphoma and marginally in other hematogological malignancies and solid tumors, with a tolerable safety and toxicity profile. The current status of the clinical evaluation of romidepsin is detailed in the present contribution.

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Year:  2010        PMID: 22491302

Source DB:  PubMed          Journal:  Drug Discov Ther        ISSN: 1881-7831


  9 in total

1.  Synthesis of a new trifluoromethylketone analogue of l-arginine and contrasting inhibitory activity against human arginase I and histone deacetylase 8.

Authors:  Monica Ilies; Daniel P Dowling; Patrick M Lombardi; David W Christianson
Journal:  Bioorg Med Chem Lett       Date:  2011-08-03       Impact factor: 2.823

2.  Binding of the Microbial Cyclic Tetrapeptide Trapoxin A to the Class I Histone Deacetylase HDAC8.

Authors:  Nicholas J Porter; David W Christianson
Journal:  ACS Chem Biol       Date:  2017-08-30       Impact factor: 5.100

3.  Structural basis of the antiproliferative activity of largazole, a depsipeptide inhibitor of the histone deacetylases.

Authors:  Kathryn E Cole; Daniel P Dowling; Matthew A Boone; Andrew J Phillips; David W Christianson
Journal:  J Am Chem Soc       Date:  2011-07-26       Impact factor: 15.419

Review 4.  Structure, mechanism, and inhibition of histone deacetylases and related metalloenzymes.

Authors:  Patrick M Lombardi; Kathryn E Cole; Daniel P Dowling; David W Christianson
Journal:  Curr Opin Struct Biol       Date:  2011-08-25       Impact factor: 6.809

5.  Variable active site loop conformations accommodate the binding of macrocyclic largazole analogues to HDAC8.

Authors:  Christophe Decroos; Dane J Clausen; Brandon E Haines; Olaf Wiest; Robert M Williams; David W Christianson
Journal:  Biochemistry       Date:  2015-03-20       Impact factor: 3.162

Review 6.  Metabolic Regulation by Lysine Malonylation, Succinylation, and Glutarylation.

Authors:  Matthew D Hirschey; Yingming Zhao
Journal:  Mol Cell Proteomics       Date:  2015-02-25       Impact factor: 5.911

7.  General Base-General Acid Catalysis in Human Histone Deacetylase 8.

Authors:  Sister M Lucy Gantt; Christophe Decroos; Matthew S Lee; Laura E Gullett; Christine M Bowman; David W Christianson; Carol A Fierke
Journal:  Biochemistry       Date:  2016-01-25       Impact factor: 3.162

8.  Structure of 'linkerless' hydroxamic acid inhibitor-HDAC8 complex confirms the formation of an isoform-specific subpocket.

Authors:  Alexa A Tabackman; Rochelle Frankson; Eric S Marsan; Kay Perry; Kathryn E Cole
Journal:  J Struct Biol       Date:  2016-06-29       Impact factor: 2.867

9.  Structural mass spectrometry decodes domain interaction and dynamics of the full-length Human Histone Deacetylase 2.

Authors:  Zoja Soloviev; Joshua M A Bullock; Juliette M B James; Andrea C Sauerwein; Joanne E Nettleship; Raymond J Owens; D Flemming Hansen; Maya Topf; Konstantinos Thalassinos
Journal:  Biochim Biophys Acta Proteins Proteom       Date:  2022-01-18       Impact factor: 3.036

  9 in total

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