HDAC inhibitors in cancer biology: emerging mechanisms and clinical applications.

Reversible acetylation mediated by histone deacetylases (HDACs) influences a broad repertoire of physiological processes, many of which are aberrantly controlled in tumor cells. As HDAC inhibition prompts tumor cells to enter apoptosis, small-molecule HDAC inhibitors have been developed as a new cla...

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Main Authors: Khan, O, La Thangue, N
Format: Journal article
Language:English
Published: 2012
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author Khan, O
La Thangue, N
author_facet Khan, O
La Thangue, N
author_sort Khan, O
collection OXFORD
description Reversible acetylation mediated by histone deacetylases (HDACs) influences a broad repertoire of physiological processes, many of which are aberrantly controlled in tumor cells. As HDAC inhibition prompts tumor cells to enter apoptosis, small-molecule HDAC inhibitors have been developed as a new class of mechanism-based anti-cancer agent, many of which have entered clinical trials. Although the clinical picture is evolving and the precise utility of HDAC inhibitors remains to be determined, it is noteworthy that certain tumor types undergo a favorable response, in particular hematological malignancies. Vorinostat and romidepsin have been approved for treating cutaneous T-cell lymphoma in patients with progressive, persistent or recurrent disease. Here, we discuss developments in our understanding of molecular events that underlie the anti-cancer effects of HDAC inhibitors and relate this information to the emerging clinical picture for the application of these inhibitors in the treatment of cancer.
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spelling oxford-uuid:036d4e0f-d642-4794-8e9f-0c085297ad082022-03-26T08:46:03ZHDAC inhibitors in cancer biology: emerging mechanisms and clinical applications.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:036d4e0f-d642-4794-8e9f-0c085297ad08EnglishSymplectic Elements at Oxford2012Khan, OLa Thangue, NReversible acetylation mediated by histone deacetylases (HDACs) influences a broad repertoire of physiological processes, many of which are aberrantly controlled in tumor cells. As HDAC inhibition prompts tumor cells to enter apoptosis, small-molecule HDAC inhibitors have been developed as a new class of mechanism-based anti-cancer agent, many of which have entered clinical trials. Although the clinical picture is evolving and the precise utility of HDAC inhibitors remains to be determined, it is noteworthy that certain tumor types undergo a favorable response, in particular hematological malignancies. Vorinostat and romidepsin have been approved for treating cutaneous T-cell lymphoma in patients with progressive, persistent or recurrent disease. Here, we discuss developments in our understanding of molecular events that underlie the anti-cancer effects of HDAC inhibitors and relate this information to the emerging clinical picture for the application of these inhibitors in the treatment of cancer.
spellingShingle Khan, O
La Thangue, N
HDAC inhibitors in cancer biology: emerging mechanisms and clinical applications.
title HDAC inhibitors in cancer biology: emerging mechanisms and clinical applications.
title_full HDAC inhibitors in cancer biology: emerging mechanisms and clinical applications.
title_fullStr HDAC inhibitors in cancer biology: emerging mechanisms and clinical applications.
title_full_unstemmed HDAC inhibitors in cancer biology: emerging mechanisms and clinical applications.
title_short HDAC inhibitors in cancer biology: emerging mechanisms and clinical applications.
title_sort hdac inhibitors in cancer biology emerging mechanisms and clinical applications
work_keys_str_mv AT khano hdacinhibitorsincancerbiologyemergingmechanismsandclinicalapplications
AT lathanguen hdacinhibitorsincancerbiologyemergingmechanismsandclinicalapplications