SMA therapy approach
Down-regulation of NCALD in spinal muscular atrophy and diseases with a disturbed calcium homeostasis
Spinal muscular atrophy (SMA) is an autosomal recessive disorder based on the loss of the survival motor neuron 1 (SMN1) genes. The severity of the disease is inversely correlated with the copy number of the main disease modifying gene SMN2. In rare cases, siblings of SMA patients do not show SMA, although they carry exactly the same SMN1 and SMN2 gene status as their SMA affected relatives. So other genetic factors are able to fully protect homozygously SMN1-deleted individuals from developing SMA. The inventors found that this phenomenon might be caused by the overexpression of plastin 3, an actin-bundling protein, and/or low expression levels of the calcium sensing protein neurocalcin delta (NCALD).
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In vitro and in vivo studies show that inhibitors of neurocalcin delta (NCALD) are suitable for treating and preventing such disorders in a patient. Said inhibitors are, likewise, effective tools for in vitro neuronal differentiation and maturation, and restoration of impaired endocytosis. Therefore, down-regulation of NCALD can revert the effect caused by the loss of SMN1. There are promising indications that a combination of an SMN2 targeted therapy with NCALD inhibitors not only reduce the symptoms of SMA patients but cure the disease as it is seen by relatives that have the same SMN1 and SMN2 gene status.
Based on that interaction, the inhibition of NCALD provides a tool to treat SMA and other neurodegenerative diseases in which disturbed calcium homeostasis plays a role, such as Parkinson and Alzheimer disease as well as amyotrophic lateral sclerosis.
- A novel therapeutic approach to treat SMA and other neuro-degenerative disorders
- NCALD inhibitors might fully protect SMN1-deleted individuals
- New mode of action
- Combination with SMN2 drugs should be beneficial
Down-regulation of NCALD by e.g. siRNA or antisense oligonucleotides (ASOs) can be used to treat SMA and possibly other neurodegenerative diseases like Alzheimer. Potential application solely or as a combined therapy with SMN2 targeted drugs.
On behalf of the University of Cologne, PROvendis offers access to rights for commercial use as well as the opportunity for further co-development.
In vivo studies provided evidence for a therapeutic effectiveness of NCALD down-regulation in SMA mice that express low SMN levels by restoring axon growth. In case of interest, we are pleased to inform you about the current status of the patent.
Publikationen & Verweise
Wirth B, Garbes L, Riessland M. (2013) How genetic modifiers influence the phenotype of spinal muscular atrophy and suggest future therapeutic approaches. Curr. Opin. Genet. Dev. 23(3):330-8.
Ruiz et al. (2010) altered intracellular Ca2+ homeostasis in nerve terminals of severe spinal muscular atrophy in mice. J. Neurosci. 30(3):849-57.raes maximinihit plitas as alibus.
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StichworteNeurocalcin delta (NCALD), spinal muscular atrophy, SMA, antisense oligonucleotides, ASO, neurodegenerative diseases, SMN2