Literature DB >> 30076486

Therapeutic potential of combined viral transduction and CRISPR/Cas9 gene editing in treating neurodegenerative diseases.

Joshua Kuruvilla1, Andrew Octavian Sasmita1, Anna Pick Kiong Ling2.   

Abstract

BACKGROUND AND
PURPOSE: The central nervous system (CNS) faces unique difficulties in attaining permanent therapy for neurodegenerative disorder (ND). Genomic level forms of therapy have garnered interest in the recent decade, with the novel CRISPR/Cas9 gene editing tool continuing to be explored due to its efficiency, safety, and adaptability to varying conditions. With the aid of viral vectors as transport vectors, the gene editing tool has produced promising in vitro and in vivo findings in study models. Thus, this review focuses on the recent advancements and update of CRISPR/Cas9 to combat neurodegenerative diseases.
METHODS: Articles detailing potential applications of CRISPR/Cas9 in neurodegenerative settings were retrieved from PubMed and Google Scholar with the keywords "CRISPR," "gene editing," and "neurodegenerative diseases." Relevant information was collected and critically reviewed.
RESULTS: The utility of CRISPR/Cas9 coupled with viral transduction ranges from the disruption of amyloid precursor protein (APP) production at a genomic level in Alzheimer's disease (AD) to the deletion of varying exon portions of the Dmd gene in Duchenne muscular dystrophy (DMD) which would increase dystrophin expression. This usage of CRISPR/Cas9 also extends to experimentally ameliorate the neurodegenerative effects caused by viral infections.
CONCLUSION: The CRISPR/Cas9 gene editing tool is a powerful arsenal in the field of gene therapy and molecular medicine; hence, more research should be called to focus on the ample potential this tool has to offer in the field of neurodegenerative diseases.

Entities:  

Keywords:  CRISPR/Cas9; Demyelination; Gene editing; Molecular neuroscience; Neurodegeneration

Mesh:

Year:  2018        PMID: 30076486     DOI: 10.1007/s10072-018-3521-0

Source DB:  PubMed          Journal:  Neurol Sci        ISSN: 1590-1874            Impact factor:   3.307


  72 in total

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Journal:  Mol Ther       Date:  2009-06-02       Impact factor: 11.454

2.  Convection-enhanced delivery of AAV vector in parkinsonian monkeys; in vivo detection of gene expression and restoration of dopaminergic function using pro-drug approach.

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3.  Generation of a gene-corrected isogenic control cell line from an Alzheimer's disease patient iPSC line carrying a A79V mutation in PSEN1.

Authors:  Carlota Pires; Benjamin Schmid; Carina Petræus; Anna Poon; Natakarn Nimsanor; Troels T Nielsen; Gunhild Waldemar; Lena E Hjermind; Jørgen E Nielsen; Poul Hyttel; Kristine K Freude
Journal:  Stem Cell Res       Date:  2016-08-07       Impact factor: 2.020

Review 4.  Prevalence and treatment of depression in Parkinson's disease.

Authors:  Connie Veazey; Sahinde Ozlem Erden Aki; Karon F Cook; Eugene C Lai; Mark E Kunik
Journal:  J Neuropsychiatry Clin Neurosci       Date:  2005       Impact factor: 2.198

5.  In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy.

Authors:  Christopher E Nelson; Chady H Hakim; David G Ousterout; Pratiksha I Thakore; Eirik A Moreb; Ruth M Castellanos Rivera; Sarina Madhavan; Xiufang Pan; F Ann Ran; Winston X Yan; Aravind Asokan; Feng Zhang; Dongsheng Duan; Charles A Gersbach
Journal:  Science       Date:  2015-12-31       Impact factor: 47.728

Review 6.  Harnessing neuroplasticity: modern approaches and clinical future.

Authors:  Andrew Octavian Sasmita; Joshua Kuruvilla; Anna Pick Kiong Ling
Journal:  Int J Neurosci       Date:  2018-05-04       Impact factor: 2.292

7.  Modeling familial Alzheimer's disease with induced pluripotent stem cells.

Authors:  Takuya Yagi; Daisuke Ito; Yohei Okada; Wado Akamatsu; Yoshihiro Nihei; Takahito Yoshizaki; Shinya Yamanaka; Hideyuki Okano; Norihiro Suzuki
Journal:  Hum Mol Genet       Date:  2011-09-07       Impact factor: 6.150

8.  Intramuscular Delivery of scAAV9-hIGF1 Prolongs Survival in the hSOD1G93A ALS Mouse Model via Upregulation of D-Amino Acid Oxidase.

Authors:  HuiQian Lin; HaoJie Hu; WeiSong Duan; YaLing Liu; GuoJun Tan; ZhongYao Li; YaKun Liu; BinBin Deng; XueQin Song; Wan Wang; Di Wen; Ying Wang; ChunYan Li
Journal:  Mol Neurobiol       Date:  2016-12-19       Impact factor: 5.590

9.  Improving single injection CSF delivery of AAV9-mediated gene therapy for SMA: a dose-response study in mice and nonhuman primates.

Authors:  Kathrin Meyer; Laura Ferraiuolo; Leah Schmelzer; Lyndsey Braun; Vicki McGovern; Shibi Likhite; Olivia Michels; Alessandra Govoni; Julie Fitzgerald; Pablo Morales; Kevin D Foust; Jerry R Mendell; Arthur H M Burghes; Brian K Kaspar
Journal:  Mol Ther       Date:  2014-10-31       Impact factor: 11.454

10.  Long-term neurologic and neurosensory sequelae in adult survivors of a childhood brain tumor: childhood cancer survivor study.

Authors:  Roger J Packer; James G Gurney; Judy A Punyko; Sarah S Donaldson; Peter D Inskip; Marilyn Stovall; Yutaka Yasui; Ann C Mertens; Charles A Sklar; H Stacy Nicholson; Lonnie K Zeltzer; Joseph P Neglia; Leslie L Robison
Journal:  J Clin Oncol       Date:  2003-09-01       Impact factor: 50.717

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  1 in total

1.  Recent Scientific Breakthroughs Applying CRISPR Gene Editing in Neurological Disorders.

Authors:  Mitra Assadi-Khansari; London Pamela McGill
Journal:  Dela J Public Health       Date:  2021-12-15
  1 in total

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