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Impaired proteostasis in rare neurological diseases.
Osinalde, Nerea; Duarri, Anna; Ramirez, Juanma; Barrio, Rosa; Perez de Nanclares, Guiomar; Mayor, Ugo.
Afiliação
  • Osinalde N; Department of Biochemistry and Molecular Biology, Faculty of Pharmacy, University of the Basque Country (UPV/EHU), 01006 Vitoria-Gasteiz, Spain.
  • Duarri A; Barcelona Stem Cell Bank, Center of Regenerative Medicine in Barcelona, 08908 Hospitalet de Llobregat, Barcelona, Spain.
  • Ramirez J; Department of Biochemistry and Molecular Biology, Faculty of Science and Technology, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain.
  • Barrio R; Functional Genomics Unit, CIC bioGUNE, 48160 Derio, Spain.
  • Perez de Nanclares G; Molecular (Epi)Genetics Laboratory, BioAraba National Health Institute, Hospital Universitario Araba-Txagorritxu, Vitoria-Gasteiz, Alava, Spain.
  • Mayor U; Department of Biochemistry and Molecular Biology, Faculty of Science and Technology, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain; Ikerbasque, Basque Foundation for Science, 48013 Bilbao, Spain. Electronic address: ugo.mayor@ehu.eus.
Semin Cell Dev Biol ; 93: 164-177, 2019 09.
Article em En | MEDLINE | ID: mdl-30355526
Rare diseases are classified as such when their prevalence is 1:2000 or lower, but even if each of them is so infrequent, altogether more than 300 million people in the world suffer one of the ∼7000 diseases considered as rare. Over 1200 of these disorders are known to affect the brain or other parts of our nervous system, and their symptoms can affect cognition, motor function and/or social interaction of the patients; we refer collectively to them as rare neurological disorders or RNDs. We have focused this review on RNDs known to have compromised protein homeostasis pathways. Proteostasis can be regulated and/or altered by a chain of cellular mechanisms, from protein synthesis and folding, to aggregation and degradation. Overall, we provide a list comprised of above 215 genes responsible for causing more than 170 distinct RNDs, deepening on some representative diseases, including as well a clinical view of how those diseases are diagnosed and dealt with. Additionally, we review existing methodologies for diagnosis and treatment, discussing the potential of specific deubiquitinating enzyme inhibition as a future therapeutic avenue for RNDs.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas / Proteostase / Doenças do Sistema Nervoso Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas / Proteostase / Doenças do Sistema Nervoso Idioma: En Ano de publicação: 2019 Tipo de documento: Article