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Spinocerebellar ataxias: from pathogenesis to recent therapeutic advances.
Cui, Zi-Ting; Mao, Zong-Tao; Yang, Rong; Li, Jia-Jia; Jia, Shan-Shan; Zhao, Jian-Li; Zhong, Fang-Tian; Yu, Peng; Dong, Ming.
Afiliación
  • Cui ZT; Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, China.
  • Mao ZT; Department of Plastic and Reconstructive Surgery, The First Hospital of Jilin University, Changchun, China.
  • Yang R; Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, China.
  • Li JJ; Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, China.
  • Jia SS; Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, China.
  • Zhao JL; Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, China.
  • Zhong FT; Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, China.
  • Yu P; Department of Ophthalmology, the Second Hospital of Jilin University, Changchun, China.
  • Dong M; Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, China.
Front Neurosci ; 18: 1422442, 2024.
Article en En | MEDLINE | ID: mdl-38894941
ABSTRACT
Spinocerebellar ataxia is a phenotypically and genetically heterogeneous group of autosomal dominant-inherited degenerative disorders. The gene mutation spectrum includes dynamic expansions, point mutations, duplications, insertions, and deletions of varying lengths. Dynamic expansion is the most common form of mutation. Mutations often result in indistinguishable clinical phenotypes, thus requiring validation using multiple genetic testing techniques. Depending on the type of mutation, the pathogenesis may involve proteotoxicity, RNA toxicity, or protein loss-of-function. All of which may disrupt a range of cellular processes, such as impaired protein quality control pathways, ion channel dysfunction, mitochondrial dysfunction, transcriptional dysregulation, DNA damage, loss of nuclear integrity, and ultimately, impairment of neuronal function and integrity which causes diseases. Many disease-modifying therapies, such as gene editing technology, RNA interference, antisense oligonucleotides, stem cell technology, and pharmacological therapies are currently under clinical trials. However, the development of curative approaches for genetic diseases remains a global challenge, beset by technical, ethical, and other challenges. Therefore, the study of the pathogenesis of spinocerebellar ataxia is of great importance for the sustained development of disease-modifying molecular therapies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Neurosci Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Neurosci Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza