Proteostasis disruption and lipid dyshomeostasis in neurodegeneration: exploring common druggable targets across sporadic and monogenic disorders

Neurodegenerative disorders pose an increasing burden in the aging society. These conditions share several molecular pathomechanisms, some of which may offer opportunities for therapeutic intervention. In this review, we explore a representative selection of sporadic and hereditary neurodegenerative diseases-namely Alzheimer's disease, cerebral amyloid angiopathy, and the polyQ disorders spinocerebellar ataxia types 2 and 3, as well as Huntington's disease-which all feature the accumulation of intra- or extracellular protein deposits as a hallmark. We place particular emphasis on dysregulations in proteostasis-underlying the formation of these aggregates-and the less commonly addressed disturbances in lipid metabolism. By highlighting potential mechanistic links across different classes of neurodegenerative diseases, we aim to provide new insights that may guide the identification of shared druggable targets and the development of broad-spectrum therapeutic strategies.

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Publication Details

Journal
Frontiers in Molecular Neuroscience
Published
2025-10-24
DOI
https://doi.org/10.3389/fnmol.2025.1681079
Primary Topic
Ubiquitin and proteasome pathways
Type
article
Field-Weighted Citation Impact
0.00

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article

Proteostasis disruption and lipid dyshomeostasis in neurodegeneration: exploring common druggable targets across sporadic and monogenic disorders

Thorsten Schmidt, Jonasz Jeremiasz Weber, Alcibiades E. Villarreal, Lars Friedrich et al.
Frontiers in Molecular Neuroscience
Ubiquitin and proteasome pathways
article

Proteostasis disruption and lipid dyshomeostasis in neurodegeneration: exploring common druggable targets across sporadic and monogenic disorders

Thorsten Schmidt, Jonasz Jeremiasz Weber, Alcibiades E. Villarreal, Lars Friedrich, Priscila Pereira Sena, Maria Luiza Saraiva Pereira, Florian Fath, Mar Hernández‐Guillamón, Gabrielle B. Britton, Liubovi Sopco
article en

Abstract

Neurodegenerative disorders pose an increasing burden in the aging society. These conditions share several molecular pathomechanisms, some of which may offer opportunities for therapeutic intervention. In this review, we explore a representative selection of sporadic and hereditary neurodegenerative diseases-namely Alzheimer's disease, cerebral amyloid angiopathy, and the polyQ disorders spinocerebellar ataxia types 2 and 3, as well as Huntington's disease-which all feature the accumulation of intra- or extracellular protein deposits as a hallmark. We place particular emphasis on dysregulations in proteostasis-underlying the formation of these aggregates-and the less commonly addressed disturbances in lipid metabolism. By highlighting potential mechanistic links across different classes of neurodegenerative diseases, we aim to provide new insights that may guide the identification of shared druggable targets and the development of broad-spectrum therapeutic strategies.

Frontiers in Molecular NeuroscienceVol. 18
Universidad de Panamá (PA), Universidade Federal do Rio Grande do Sul (BR), Hospital de Clínicas de Porto Alegre (BR), Vall d'Hebron Institut de Recerca (ES), Secretaría Nacional de Ciencia, Tecnología e Innovación (PA), St. Josef-Hospital (DE), Instituto de Investigaciones Científicas y Servicios de Alta Tecnología (PA), University of Tübingen (DE), Ruhr University Bochum (DE)
Eberhard Karls Universität Tübingen
Openalex Percentile: Top 73%
Ubiquitin and proteasome pathways
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