Role of RNA Oxidation in Neurodegenerative Diseases.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
16 Jul 2020
Historique:
received: 06 06 2020
revised: 10 07 2020
accepted: 14 07 2020
entrez: 26 7 2020
pubmed: 28 7 2020
medline: 23 2 2021
Statut: epublish

Résumé

In the history of nucleic acid research, DNA has always been the main research focus. After the sketch of the human genome was completed in 2000, RNA has been started to gain more attention due to its abundancies in the cell and its essential role in cellular physiology and pathologies. Recent studies have shown that RNAs are susceptible to oxidative damage and oxidized RNA is able to break the RNA strand, and affect the protein synthesis, which can lead to cell degradation and cell death. Studies have shown that RNA oxidation is one of the early events in the formation and development of neurodegenerative disorders, including Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis. However, its molecular mechanism, as well as its impact on these diseases, are still unclear. In this article, we review the different types of RNA oxidative damage and the neurodegenerative diseases that are reported to be associated with RNA oxidative damage. In addition, we discuss recent findings on the association between RNA oxidative damage and the development of neurodegenerative diseases, which will have great significance for the development of novel strategies for the prevention and treatment of these diseases.

Identifiants

pubmed: 32708667
pii: ijms21145022
doi: 10.3390/ijms21145022
pmc: PMC7403986
pii:
doi:

Substances chimiques

RNA 63231-63-0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : National Natural Science Foundation of China
ID : 91849209; 81850410551

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Auteurs

Ziqian Liu (Z)

Center for Molecular Genetics, Institute for Translational Medicine, Qingdao University, Qingdao 266000, China.
School of Basic Medicine, Qingdao University, Qingdao 266000, China.

Xiatian Chen (X)

Center for Molecular Genetics, Institute for Translational Medicine, Qingdao University, Qingdao 266000, China.
School of Basic Medicine, Qingdao University, Qingdao 266000, China.

Zhe Li (Z)

Center for Molecular Genetics, Institute for Translational Medicine, Qingdao University, Qingdao 266000, China.
School of Basic Medicine, Qingdao University, Qingdao 266000, China.

Wei Ye (W)

Jiangsu Provincial Engineering Research Center for Biomedical Materials and Advanced Medical Device, Huaiyin Institute of Technology, Huaian 223003, China.

Hongyan Ding (H)

Jiangsu Provincial Engineering Research Center for Biomedical Materials and Advanced Medical Device, Huaiyin Institute of Technology, Huaian 223003, China.

Peifeng Li (P)

Center for Molecular Genetics, Institute for Translational Medicine, Qingdao University, Qingdao 266000, China.

Lynn Htet Htet Aung (LHH)

Center for Molecular Genetics, Institute for Translational Medicine, Qingdao University, Qingdao 266000, China.
School of Basic Medicine, Qingdao University, Qingdao 266000, China.

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