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Application of CRISPR/Cas9 System in the Treatment of Alzheimer's Disease and Neurodegenerative Diseases.

Authors :
Rahimi, Araz
Sameei, Parsa
Mousavi, Sana
Ghaderi, Kimia
Hassani, Amin
Hassani, Sepideh
Alipour, Shahriar
Source :
Molecular Neurobiology; Nov2024, Vol. 61 Issue 11, p9416-9431, 16p
Publication Year :
2024

Abstract

Alzheimer's, Parkinson's, and Huntington's are some of the most common neurological disorders, which affect millions of people worldwide. Although there have been many treatments for these diseases, there are still no effective treatments to treat or completely stop these disorders. Perhaps the lack of proper treatment for these diseases can be related to various reasons, but the poor results related to recent clinical research also prompted doctors to look for new treatment approaches. In this regard, various researchers from all over the world have provided many new treatments, one of which is CRISPR/Cas9. Today, the CRISPR/Cas9 system is mostly used for genetic modifications in various species. In addition, by using the abilities available in the CRISPR/Cas9 system, researchers can either remove or modify DNA sequences, which in this way can establish a suitable and useful treatment method for the treatment of genetic diseases that have undergone mutations. We conducted a non-systematic review of articles and study results from various databases, including PubMed, Medline, Web of Science, and Scopus, in recent years. and have investigated new treatment methods in neurodegenerative diseases with a focus on Alzheimer's disease. Then, in the following sections, the treatment methods were classified into three groups: anti-tau, anti-amyloid, and anti-APOE regimens. Finally, we discussed various applications of the CRISPR/Cas-9 system in Alzheimer's disease. Today, using CRISPR/Cas-9 technology, scientists create Alzheimer's disease models that have a more realistic phenotype and reveal the processes of pathogenesis; following the screening of defective genes, they establish treatments for this disease. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08937648
Volume :
61
Issue :
11
Database :
Complementary Index
Journal :
Molecular Neurobiology
Publication Type :
Academic Journal
Accession number :
180429363
Full Text :
https://doi.org/10.1007/s12035-024-04143-2