Abstract |
Spinal muscular atrophy (SMA) is the leading genetic cause of early childhood death worldwide and no therapy is available today. Many drugs, especially histone deacetylase inhibitors (HDACi), increase SMN levels. As all HDACi tested so far only mildly ameliorate the SMA phenotype or are unsuitable for use in humans, there is still need to identify more potent drugs. Here, we assessed the therapeutic power of the pan-HDACi JNJ-26481585 for SMA, which is currently used in various clinical cancer trials. When administered for 64 h at 100 nM, JNJ-26481585 upregulated SMN levels in SMA fibroblast cell lines, including those from non-responders to valproic acid. Oral treatment of Taiwanese SMA mice and control littermates starting at P0 showed no overt extension of lifespan, despite mild improvements in motor abilities and weight progression. Many treated and untreated animals showed a very rapid decline or unexpected sudden death. We performed exploratory autopsy and histological assessment at different disease stages and found consistent abnormalities in the intestine, heart and lung and skeletal muscle vasculature of SMA animals, which were not prevented by JNJ-26481585 treatment. Interestingly, some of these features may be only indirectly caused by α-motoneuron function loss but may be major life-limiting factors in the course of disease. A better understanding of - primary or secondary - non-neuromuscular organ involvement in SMA patients may improve standard of care and may lead to reassessment of how to investigate SMA patients clinically.
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Authors | Julia Schreml, Markus Riessland, Mario Paterno, Lutz Garbes, Kristina Roßbach, Bastian Ackermann, Jan Krämer, Eilidh Somers, Simon H Parson, Raoul Heller, Albrecht Berkessel, Anja Sterner-Kock, Brunhilde Wirth |
Journal | European journal of human genetics : EJHG
(Eur J Hum Genet)
Vol. 21
Issue 6
Pg. 643-52
(Jun 2013)
ISSN: 1476-5438 [Electronic] England |
PMID | 23073311
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Histone Deacetylase Inhibitors
- Hydroxamic Acids
- SMN Complex Proteins
- quisinostat
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Topics |
- Animals
- Body Weight
(drug effects)
- Brain
(drug effects, metabolism, pathology)
- Cells, Cultured
- Dose-Response Relationship, Drug
- Fibroblasts
(drug effects, metabolism, pathology)
- Histone Deacetylase Inhibitors
(pharmacology, therapeutic use)
- Humans
- Hydroxamic Acids
(adverse effects, pharmacology, therapeutic use)
- Mice
- Motor Activity
(drug effects)
- Muscle, Skeletal
(blood supply, drug effects, pathology)
- Muscular Atrophy, Spinal
(drug therapy, metabolism, pathology)
- Neuromuscular Junction
(drug effects, metabolism, pathology)
- Organ Specificity
(drug effects)
- Phenotype
- SMN Complex Proteins
(metabolism)
- Spinal Cord
(drug effects, metabolism, pathology)
- Survival Analysis
- Treatment Outcome
- Up-Regulation
(drug effects)
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