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Development of new chemical tools to combat ALS

Project description

Targeted molecular therapies against amyotrophic lateral sclerosis

Patients suffering from amyotrophic lateral sclerosis (ALS) experience progressive neurodegeneration. Although the precise genetic aetiology remains elusive, an hexanucleotide expansion in one of the introns of the C9ORF72 gene is the most frequent genetic mutation associated with the disease. Scientists of the EU-funded Combat_ALS project are working towards the development of therapeutic tools to counteract the deleterious effects produced by the repeat-containing RNAs resulting from C9ORF72 transcription. A number of chemical agents including antisense oligonucleotides will be tested and their efficacy will be evaluated in cell models and human cerebral organoids.

Objective

Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disorder that occurs in families, and sporadically in individuals. It was recently discovered that the massive expansion of a GC-rich hexanucleotide in the intron of the gen C9orf72 is its most frequent genetic cause. Many efforts have been dedicated to decipher the mechanisms by which this repeat expansion contributes to the disease. Although not completely understood, the most prominent mechanism suggested is the toxicity mediated by bidirectional transcription of RNA containing expansion of the repeated motif. These transcripts form nuclear RNA foci may sequester RNA-binding proteins (RBPs) leading to a loss of function. Recent investigations have reported on RBPs that specifically interact with quadruplex structures formed by repeat-containing C9orf72 RNAs. All these evidences make C9orf72 a very promising therapeutic target for ALS.
This proposal is focused on the development of new therapeutic tools based on targeting C9orf72 repeat-containing RNA. The objective is finding chemical agents able to counteract the toxicity induced by these RNAs. I will explore antisense and siRNA oligonucleotides containing novel chemical modifications with improved properties. I will study their structure, stability and silencing potencies. Moreover, I propose to use new screening methods to find small compounds with good affinity and specificity for C9orf72 repeats. This proposal includes an in-depth study of the binding mode of the most promising ligands by high resolution NMR, and in vivo testing. For this final aim, I will address the generation of human cerebral organoids carrying C9orf72 repeat expansion and their use to test the therapeutic strategies mentioned above.

Fields of science (EuroSciVoc)

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Programme(s)

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Topic(s)

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Funding Scheme

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MSCA-IF-GF - Global Fellowships

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Call for proposal

Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.

(opens in new window) H2020-MSCA-IF-2017

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Coordinator

AGENCIA ESTATAL CONSEJO SUPERIOR DE INVESTIGACIONES CIENTIFICAS
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 224 683,20
Address
CALLE SERRANO 117
28006 MADRID
Spain

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Region
Comunidad de Madrid Comunidad de Madrid Madrid
Activity type
Research Organisations
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 224 683,20

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