Literature DB >> 30756362

Nucleic Acid-Based Therapeutics for Parkinson's Disease.

Masayuki Nakamori1, Eunsung Junn2, Hideki Mochizuki1, M Maral Mouradian3.   

Abstract

Parkinson's disease (PD) is a progressive neurodegenerative disorder that is diagnosed largely on clinical grounds due to characteristic motor manifestations that result from the loss of nigrostriatal dopaminergic neurons. While traditional pharmacological approaches to enhance dopamine levels, such as with L-dopa, can be very effective initially, the chronic use of this dopamine precursor is commonly plagued with motor response complications. Additionally, with advancing disease, non-motor manifestations emerge, including psychosis and dementia that compound patient disability. The pathology includes hallmark intraneuronal inclusions known as Lewy bodies and Lewy neurites that contain fibrillar α-synuclein aggregates. Evidence has also accumulated that these aggregates can propagate across synaptically connected brain regions, a phenomenon that can explain the progressive nature of the disease and the emergence of additional symptoms over time. The level of α-synuclein is believed to play a critical role in its fibrillization and aggregation. Accordingly, nucleic acid-based therapeutics for PD include strategies to deliver dopamine biosynthetic enzymes to boost dopamine production or modulate the basal ganglia circuitry in order to improve motor symptoms. Delivery of trophic factors that might enhance the survival of dopamine neurons is another strategy that has been attempted. These gene therapy approaches utilize viral vectors and are delivered stereotaxically in the brain. Alternative disease-modifying strategies focus on downregulating the expression of the α-synuclein gene using various techniques, including modified antisense oligonucleotides, short hairpin RNA, short interfering RNA, and microRNA. The latter approaches also have implications for dementia with Lewy bodies. Other PD genes can also be targeted using nucleic acids. In this review, we detail these various strategies that are still experimental, and discuss the challenges and opportunities of nucleic acid-based therapeutics for PD.

Entities:  

Keywords:  Antisense oligonucleotides; Gene therapy; MicroRNA; Neurodegeneration; α-Synuclein

Mesh:

Substances:

Year:  2019        PMID: 30756362      PMCID: PMC6554378          DOI: 10.1007/s13311-019-00714-7

Source DB:  PubMed          Journal:  Neurotherapeutics        ISSN: 1878-7479            Impact factor:   7.620


  75 in total

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3.  Alteration in alpha-synuclein mRNA expression in Parkinson's disease.

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Journal:  Mov Disord       Date:  2004-02       Impact factor: 10.338

4.  Sequence-specific inhibition of microRNA- and siRNA-induced RNA silencing.

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Journal:  RNA       Date:  2004-03       Impact factor: 4.942

Review 5.  The ups and downs of alpha-synuclein mRNA expression.

Authors:  Justus C Dächsel; Sarah J Lincoln; John Gonzalez; Owen A Ross; Dennis W Dickson; Matthew J Farrer
Journal:  Mov Disord       Date:  2007-01-15       Impact factor: 10.338

6.  Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.

Authors:  Demetrius M Maraganore; Mariza de Andrade; Alexis Elbaz; Matthew J Farrer; John P Ioannidis; Rejko Krüger; Walter A Rocca; Nicole K Schneider; Timothy G Lesnick; Sarah J Lincoln; Mary M Hulihan; Jan O Aasly; Tetsuo Ashizawa; Marie-Christine Chartier-Harlin; Harvey Checkoway; Carlo Ferrarese; Georgios Hadjigeorgiou; Nobutaka Hattori; Hideshi Kawakami; Jean-Charles Lambert; Timothy Lynch; George D Mellick; Spiridon Papapetropoulos; Abbas Parsian; Aldo Quattrone; Olaf Riess; Eng-King Tan; Christine Van Broeckhoven
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7.  Silencing of human alpha-synuclein in vitro and in rat brain using lentiviral-mediated RNAi.

Authors:  Mohan K Sapru; Jonathan W Yates; Shea Hogan; Lixin Jiang; Jeremy Halter; Martha C Bohn
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Journal:  Biochem Biophys Res Commun       Date:  2006-01-25       Impact factor: 3.575

9.  Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.

Authors:  Alexander Zimprich; Saskia Biskup; Petra Leitner; Peter Lichtner; Matthew Farrer; Sarah Lincoln; Jennifer Kachergus; Mary Hulihan; Ryan J Uitti; Donald B Calne; A Jon Stoessl; Ronald F Pfeiffer; Nadja Patenge; Iria Carballo Carbajal; Peter Vieregge; Friedrich Asmus; Bertram Müller-Myhsok; Dennis W Dickson; Thomas Meitinger; Tim M Strom; Zbigniew K Wszolek; Thomas Gasser
Journal:  Neuron       Date:  2004-11-18       Impact factor: 17.173

10.  Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.

Authors:  Coro Paisán-Ruíz; Shushant Jain; E Whitney Evans; William P Gilks; Javier Simón; Marcel van der Brug; Adolfo López de Munain; Silvia Aparicio; Angel Martínez Gil; Naheed Khan; Janel Johnson; Javier Ruiz Martinez; David Nicholl; Itxaso Martí Carrera; Amets Saénz Pena; Rohan de Silva; Andrew Lees; José Félix Martí-Massó; Jordi Pérez-Tur; Nick W Wood; Andrew B Singleton
Journal:  Neuron       Date:  2004-11-18       Impact factor: 17.173

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Review 1.  MicroRNAs Dysregulation and Metabolism in Multiple System Atrophy.

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2.  PD-L1 siRNA Theranostics With a Dextran Nanoparticle Highlights the Importance of Nanoparticle Delivery for Effective Tumor PD-L1 Downregulation.

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3.  Two-step screening method to identify α-synuclein aggregation inhibitors for Parkinson's disease.

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Journal:  Sci Rep       Date:  2022-01-10       Impact factor: 4.379

4.  MiR-9-5p Inhibits the MMP+-Induced Neuron Apoptosis through Regulating SCRIB/β-Catenin Signaling in Parkinson's Disease.

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Review 5.  Epigenetic Regulation of Neuroinflammation in Parkinson's Disease.

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6.  MicroRNA-18a-5p Administration Suppresses Retinal Neovascularization by Targeting FGF1 and HIF1A.

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7.  Construction of a Potential Breast Cancer-Related miRNA-mRNA Regulatory Network.

Authors:  Xinhong Liu; Feng Chen; Fang Tan; Fang Li; Ruokun Yi; Dingyi Yang; Xin Zhao
Journal:  Biomed Res Int       Date:  2020-11-04       Impact factor: 3.411

8.  Intracerebral Administration of a Ligand-ASO Conjugate Selectively Reduces α-Synuclein Accumulation in Monoamine Neurons of Double Mutant Human A30P*A53T*α-Synuclein Transgenic Mice.

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  8 in total

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