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Erschienen in: Alzheimer's Research & Therapy 1/2014

01.02.2014 | Review

Fyn kinase inhibition as a novel therapy for Alzheimer’s disease

verfasst von: Haakon B Nygaard, Christopher H van Dyck, Stephen M Strittmatter

Erschienen in: Alzheimer's Research & Therapy | Ausgabe 1/2014

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Abstract

Alzheimer’s disease (AD) is a devastating neurodegenerative disorder, afflicting more than one-third of people over the age of 85. While many therapies for AD are in late-stage clinical testing, rational drug design based on distinct signaling pathways in this disorder is only now emerging. Here we review the putative signaling pathway of amyloid-beta (Aβ), by which the tyrosine kinase Fyn is activated via cell surface binding of Aβ oligomers to cellular prion protein. Several lines of evidence implicate Fyn in the pathogenesis of AD, and its interaction with both Aβ and Tau renders Fyn a unique therapeutic target that addresses both of the major pathologic hallmarks of AD. We are currently enrolling patients in a phase Ib study of saracatinib (AZD0530), a small molecule inhibitor with high potency for Src and Fyn, for the treatment of AD. The results of this trial and a planned phase IIa multisite study will provide important data regarding the potential for this therapeutic strategy in AD.
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Metadaten
Titel
Fyn kinase inhibition as a novel therapy for Alzheimer’s disease
verfasst von
Haakon B Nygaard
Christopher H van Dyck
Stephen M Strittmatter
Publikationsdatum
01.02.2014
Verlag
BioMed Central
Erschienen in
Alzheimer's Research & Therapy / Ausgabe 1/2014
Elektronische ISSN: 1758-9193
DOI
https://doi.org/10.1186/alzrt238

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