Histone deacetylase inhibitors in the treatment of muscular dystrophies: epigenetic drugs for genetic diseases

S Consalvi, V Saccone, L Giordani, G Minetti… - Molecular …, 2011 - Springer
Histone deacetylases inhibitors (HDACi) include a growing number of drugs that share the
ability to inhibit the enzymatic activity of some or all the HDACs. Experimental and preclinical …

Histone deacetylases: Molecular mechanisms and therapeutic implications for muscular dystrophies

M Sandonà, G Cavioli, A Renzini, A Cedola… - International Journal of …, 2023 - mdpi.com
Histone deacetylases (HDACs) are enzymes that regulate the deacetylation of numerous
histone and non-histone proteins, thereby affecting a wide range of cellular processes …

Histone deacetylase inhibitors: a potential epigenetic treatment for Duchenne muscular dystrophy

S Consalvi, V Saccone, C Mozzetta - Epigenomics, 2014 - Taylor & Francis
Duchenne muscular dystrophy (DMD) is a life-threatening genetic disease that currently has
no available cure. A number of pharmacological strategies that aim to target events …

Determinants of epigenetic resistance to HDAC inhibitors in dystrophic fibro‐adipogenic progenitors

S Consalvi, L Tucciarone, E Macrì, M De Bardi… - EMBO …, 2022 - embopress.org
Pharmacological treatment of Duchenne muscular dystrophy (DMD) with histone
deacetylase inhibitors (HDACi) is currently being tested in clinical trials; however, pre …

Inhibition of histone deacetylases: a pharmacological approach to the treatment of non-cancer disorders

NL Wiech, JF Fisher, P Helquist… - Current topics in …, 2009 - ingentaconnect.com
The dynamics of gene expression are regulated by histone acetylases (HATs) and histone
deacetylases (HDACs) that control the acetylation state of lysine side chains of the histone …

HDAC2 blockade by nitric oxide and histone deacetylase inhibitors reveals a common target in Duchenne muscular dystrophy treatment

C Colussi, C Mozzetta, A Gurtner, B Illi… - Proceedings of the …, 2008 - National Acad Sciences
The overlapping histological and biochemical features underlying the beneficial effect of
deacetylase inhibitors and NO donors in dystrophic muscles suggest an unanticipated …

Epigenetic drugs in the treatment of skeletal muscle atrophy

V Guasconi, PL Puri - Current Opinion in Clinical Nutrition & …, 2008 - journals.lww.com
We propose that the decline in anabolic signals ('passive atrophy') and activation of
catabolic pathways ('active atrophy') contribute differently to the pathogenesis of muscle …

Histone deacetylase functions and therapeutic implications for adult skeletal muscle metabolism

S Molinari, C Imbriano, V Moresi, A Renzini… - Frontiers in Molecular …, 2023 - frontiersin.org
Skeletal muscle is a highly adaptive organ that sustains continuous metabolic changes in
response to different functional demands. Healthy skeletal muscle can adjust fuel utilization …

Targeting HDAC8 to ameliorate skeletal muscle differentiation in Duchenne muscular dystrophy

M Spreafico, M Cafora, C Bragato, D Capitanio… - Pharmacological …, 2021 - Elsevier
Duchenne muscular dystrophy (DMD) causes progressive skeletal muscle degeneration
and currently there are few therapeutic options. The identification of new drug targets and …

Cytoplasmic HDAC4 regulates the membrane repair mechanism in Duchenne muscular dystrophy

A Renzini, N Marroncelli, G Cavioli… - Journal of Cachexia …, 2022 - Wiley Online Library
Abstract Background Histone deacetylase 4 (HDAC4) is a stress‐responsive factor that
mediates multiple cellular responses. As a member of class IIa HDACs, HDAC4 shuttles …