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Parkinson’s Disease: A Complex Interplay of Mitochondrial DNA Alterations and Oxidative Stress
Parkinson’s disease (PD) is one of the most common age-related neurodegenerative diseases. This pathology causes a significant loss of dopaminergic neurons in the Substantia Nigra. Several reports have claimed a role of defective nuclear and mitochondrial DNA repair pathways in PD etiology, in parti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3587993/ https://www.ncbi.nlm.nih.gov/pubmed/23348931 http://dx.doi.org/10.3390/ijms14022388 |
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author | Ciccone, Sarah Maiani, Emiliano Bellusci, Giovanna Diederich, Marc Gonfloni, Stefania |
author_facet | Ciccone, Sarah Maiani, Emiliano Bellusci, Giovanna Diederich, Marc Gonfloni, Stefania |
author_sort | Ciccone, Sarah |
collection | PubMed |
description | Parkinson’s disease (PD) is one of the most common age-related neurodegenerative diseases. This pathology causes a significant loss of dopaminergic neurons in the Substantia Nigra. Several reports have claimed a role of defective nuclear and mitochondrial DNA repair pathways in PD etiology, in particular, of the Base Excision Repair (BER) system. In addition, recent findings, related to PD progression, indicate that oxidative stress pathways involving c-Abl and GST could also be implicated in this pathology. This review focuses on recently described networks most likely involved in an integrated manner in the course of PD. |
format | Online Article Text |
id | pubmed-3587993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-35879932013-03-13 Parkinson’s Disease: A Complex Interplay of Mitochondrial DNA Alterations and Oxidative Stress Ciccone, Sarah Maiani, Emiliano Bellusci, Giovanna Diederich, Marc Gonfloni, Stefania Int J Mol Sci Review Parkinson’s disease (PD) is one of the most common age-related neurodegenerative diseases. This pathology causes a significant loss of dopaminergic neurons in the Substantia Nigra. Several reports have claimed a role of defective nuclear and mitochondrial DNA repair pathways in PD etiology, in particular, of the Base Excision Repair (BER) system. In addition, recent findings, related to PD progression, indicate that oxidative stress pathways involving c-Abl and GST could also be implicated in this pathology. This review focuses on recently described networks most likely involved in an integrated manner in the course of PD. MDPI 2013-01-24 /pmc/articles/PMC3587993/ /pubmed/23348931 http://dx.doi.org/10.3390/ijms14022388 Text en © 2013 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Ciccone, Sarah Maiani, Emiliano Bellusci, Giovanna Diederich, Marc Gonfloni, Stefania Parkinson’s Disease: A Complex Interplay of Mitochondrial DNA Alterations and Oxidative Stress |
title | Parkinson’s Disease: A Complex Interplay of Mitochondrial DNA Alterations and Oxidative Stress |
title_full | Parkinson’s Disease: A Complex Interplay of Mitochondrial DNA Alterations and Oxidative Stress |
title_fullStr | Parkinson’s Disease: A Complex Interplay of Mitochondrial DNA Alterations and Oxidative Stress |
title_full_unstemmed | Parkinson’s Disease: A Complex Interplay of Mitochondrial DNA Alterations and Oxidative Stress |
title_short | Parkinson’s Disease: A Complex Interplay of Mitochondrial DNA Alterations and Oxidative Stress |
title_sort | parkinson’s disease: a complex interplay of mitochondrial dna alterations and oxidative stress |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3587993/ https://www.ncbi.nlm.nih.gov/pubmed/23348931 http://dx.doi.org/10.3390/ijms14022388 |
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