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PMID: 19342155 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

HDACi--targets beyond chromatin.

Cancer letters ·Vol. 280 ·No. 2 ·2009-08-08 ·Pages 160-7

Buchwald M, Krämer OH, Heinzel T

Abstract

Histone deacetylases (HDACs) play an important role in gene regulation. Inhibitors of HDACs (HDACi) are novel anti-cancer drugs, which induce histone (hyper-) acetylation and counteract aberrant gene repression. On the other hand, HDACi treatment can also result in decreased gene expression, and targeting HDACs affects more than chromatin. Recently, HDACi were shown to evoke non-histone protein acetylation, which can alter signaling networks relevant for tumorgenesis. Furthermore, HDACi can promote the degradation of (proto-) oncoproteins. Here, we summarize these findings and discuss how these substances could be beneficial for the treatment and prevention of human ailments, such as cancer and unbalanced immune functions.

MeSH Terms
Acetylation Antineoplastic Agents/therapeutic use Chromatin/metabolism Cytokines/physiology Histone Deacetylase Inhibitors Histone Deacetylases/metabolism Humans Inflammation/metabolism NF-kappa B/physiology Neoplasms/drug therapy,metabolism Proteasome Endopeptidase Complex/physiology Proto-Oncogene Proteins/metabolism STAT Transcription Factors/physiology Signal Transduction/physiology Ubiquitin/physiology
Chemicals
Antineoplastic Agents Chromatin Cytokines Histone Deacetylase Inhibitors NF-kappa B Proto-Oncogene Proteins STAT Transcription Factors Ubiquitin Proteasome Endopeptidase Complex Histone Deacetylases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Buchwald Marc
Center for Molecular Biomedicine, Institute for Biochemistry and Biophysics, Friedrich-Schiller-Universität Jena, Jena, Germany. Marc.Buchwald@uni-jena.de
Krämer Oliver H
Heinzel Thorsten
Article Info
Journal
Cancer letters
Abbr.
Cancer Lett
ISSN
1872-7980
Published
2009-08-08
Epub
2009-00-01
Pages
160-7
Language
English
Region
Ireland
NLM ID
7600053
Subset
IM
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