Summary
February 2008, Vol. 17, No. 2, Pages 169-184 , DOI 10.1517/13543784.17.2.169

Histone deacetylase inhibitors: possible implications for neurodegenerative disorders

Eric Hahnen1 PhD MBA, Jan Hauke1, Christian Tränkle2, Ilker Y Eyüpoglu3, Brunhilde Wirth1 & Ingmar Blümcke4
1University of Cologne, Institute of Human Genetics, Institute of Genetics, and Center for Molecular Medicine Cologne (CMMC), Kerpenerstr. 34, 50931 Cologne, Germany +49 221 478 86464; +49 221 478 86465;
2University of Bonn, Department of Pharmacology and Toxicology, Institute of Pharmacy, Germany
3University of Erlangen, Department of Neurosurgery, Germany
4University of Erlangen, Institute of Neuropathology, Germany
Author for correspondence



During the past six years numerous studies identified histone deacetylase (HDAC) inhibitors as candidate drugs for the treatment of neurodegenerative disorders. Two major neuroprotective mechanisms of HDAC inhibitors have been identified, namely the transcriptional activation of disease-modifying genes and the correction of perturbations in histone acetylation homeostasis, which have been shown to be intimately involved in the neurodegenerative pathomechanisms of Huntington's, Parkinson's and Kennedy disease, amyotropic lateral sclerosis, Rubinstein-Taybi syndrome as well as stroke. Based on the promising in vitro and in vivo analyses, clinical trials have been initiated to evaluate the safety and efficacy of HDAC inhibitors for the treatment of devastating diseases such as Huntington's disease, amyotropic lateral sclerosis and spinal muscular atrophy. Here, the authors summarize and discuss the findings on the emerging field of epigenetic therapy strategies in neurodegenerative disorders.

Full Text | PDF (201 KB) | PDF Plus (408 KB)

Forward Links to Citing Articles

Elizabeth A. Thomas. (2009) Focal Nature of Neurological Disorders Necessitates Isotype-Selective Histone Deacetylase (HDAC) Inhibitors. Molecular Neurobiology 40:1, 33-45
Online publication date: 1-Sep-2009.
CrossRef
Ana Ricobaraza, Mar Cuadrado-Tejedor, Alberto Pérez-Mediavilla, Diana Frechilla, Joaquin Del Río, Ana García-Osta. (2009) Phenylbutyrate Ameliorates Cognitive Deficit and Reduces Tau Pathology in an Alzheimer's Disease Mouse Model. Neuropsychopharmacology 34:7, 1721-1732
Online publication date: 1-Jul-2009.
CrossRef
Sebastian Lunke, Assam El-Osta. (2009) The emerging role of epigenetic modifications and chromatin remodeling in spinal muscular atrophy. Journal of Neurochemistry 109:6, 1557-1569
Online publication date: 1-Jul-2009.
CrossRef
Yufeng Chen, Rong He, Yihua Chen, MelissaA. D'Annibale, Brett Langley, AlanP. Kozikowski. (2009) Studies of Benzamide- and Thiol-Based Histone Deacetylase Inhibitors in Models of Oxidative-Stress-Induced Neuronal Death: Identification of Some HDAC3-Selective Inhibitors. ChemMedChem 4:5, 842-852
Online publication date: 11-Jun-2009.
CrossRef
Sama F Sleiman, Manuela Basso, Lata Mahishi, Alan P Kozikowski, Mary E Donohoe, Brett Langley, Rajiv R Ratan. (2009) Putting the ‘HAT’ back on survival signalling: the promises and challenges of HDAC inhibition in the treatment of neurological conditions. Expert Opinion on Investigational Drugs 18:5, 573-584
Online publication date: 1-May-2009.
Summary | Full Text | PDF (1252 KB) | PDF Plus (4802 KB) 
Gilles Pieffet, Pavel A. Petukhov. (2009) Parameterization of aromatic azido groups: application as photoaffinity probes in molecular dynamics studies. Journal of Molecular Modeling
Online publication date: 14-Apr-2009.
CrossRef
Didem Dayangaç-Erden, Gamze Bora, Peruze Ayhan, Çetin Kocaefe, Sevim Dalkara, Kemal Yelekçi, Ayhan S. Demir, Hayat Erdem-Yurter. (2009) Histone Deacetylase Inhibition Activity and Molecular Docking of ( E )-Resveratrol: Its Therapeutic Potential in Spinal Muscular Atrophy. Chemical Biology & Drug Design 73:3, 355-364
Online publication date: 1-Apr-2009.
CrossRef
J. Hauke, M. Riessland, S. Lunke, I. Y. Eyupoglu, I. Blumcke, A. El-Osta, B. Wirth, E. Hahnen. (2008) Survival motor neuron gene 2 silencing by DNA methylation correlates with spinal muscular atrophy disease severity and can be bypassed by histone deacetylase inhibition. Human Molecular Genetics 18:2, 304-317
Online publication date: 22-Nov-2008.
CrossRef
Aleksey G. Kazantsev, Leslie M. Thompson. (2008) Therapeutic application of histone deacetylase inhibitors for central nervous system disorders. Nature Reviews Drug Discovery 7:10, 854-868
Online publication date: 1-Nov-2008.
CrossRef

Users who read this article also read:

Putting the ‘HAT’ back on survival signalling: the promises and challenges of HDAC inhibition in the treatment of neurological conditions
Sama F Sleiman, Manuela Basso, Lata Mahishi, Alan P Kozikowski, Mary E Donohoe, Brett Langley, Rajiv R Ratan
Expert Opinion on Investigational Drugs, May 2009, Vol. 18, No. 5, Pages 573-584.
Summary | Full Text | PDF (1252 KB) | PDF Plus (4802 KB) | Add to Favorites | Related 
 

Prev. Article | Next Article
View/Print PDF (201 KB)
View PDF Plus (408 KB)
Add to favourite
Email to a friend
TOC Alert | Citation Alert What is RSS?

 
 
Quick Search
for 
Authors:
Eric Hahnen
Jan Hauke
Christian Tränkle
Ilker Y Eyüpoglu
Brunhilde Wirth
Ingmar Blümcke
Keywords:
adrenoleukodystrophy
Alzheimer's disease
amyotropic lateral sclerosis
dentatorubral-pallidoluysian atrophy
depsipeptide
histone acetyltransferase
histone deacetylase
histone deacetylase inhibitor
phenylbutyrate
romidepsin
sodium butyrate
spinal muscular atrophy
spinocerebellar ataxia
suberoylanilide hydroxamic acid
valproic acid