Literature DB >> 21827981

[Histone deacetylase inhibitors in the treatment of hematological malignancies].

Richard Lemal1, Aurélie Ravinet, Cécile Moluçon-Chabrot, Jacques-Olivier Bay, Romain Guièze.   

Abstract

Histone deacetylases inhibitors (HDACi) represent a new epigenetic targeting therapy class, which is widely investigated in fundamental research and clinical trials. They are able to restore and increase tumor suppressor genes expression and to play an anti-tumoral activity through numerous targets, which are distributed all over the main differentiation, proliferation and survival cellular pathways. Their use in hematology led to vorinostat (SAHA) and romidepsin approval by FDA for the treatment of refractory cutaneous T-cell lymphomas. Preclinical and preliminary clinical results show a promising antineoplasic activity in most hematologic malignancies. This review will focus on the HDACi recent developments and current investigations, highlighted by recent communications.

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Year:  2011        PMID: 21827981     DOI: 10.1684/bdc.2011.1409

Source DB:  PubMed          Journal:  Bull Cancer        ISSN: 0007-4551            Impact factor:   1.276


  2 in total

1.  Proteasome inhibitor MG-132 enhances histone deacetylase inhibitor SAHA-induced cell death of chronic myeloid leukemia cells by an ROS-mediated mechanism and downregulation of the Bcr-Abl fusion protein.

Authors:  Wenjing Zhou; Weiwei Zhu; Liya Ma; Feng Xiao; Wenbin Qian
Journal:  Oncol Lett       Date:  2015-09-02       Impact factor: 2.967

2.  Polyamine-based small molecule epigenetic modulators.

Authors:  Shiv K Sharma; Stuart Hazeldine; Michael L Crowley; Allison Hanson; Ross Beattie; Sheeba Varghese; Thulani M D Senanayake; Aiko Hirata; Fusao Hirata; Yi Huang; Yu Wu; Nora Steinbergs; Tracey Murray-Stewart; Ian Bytheway; Robert A Casero; Patrick M Woster
Journal:  Medchemcomm       Date:  2011-11-26       Impact factor: 3.597

  2 in total

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