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Downregulation of blood serum microRNA 29 family in patients with Parkinson’s disease
There is currently no reliable and easily applicable diagnostic marker for Parkinson’s disease (PD). The aims of the present study were to compare the expression profiles of the microRNA29 family (miR-29s) in blood serum from patients with PD with healthy controls and to clarify whether the expressi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511199/ https://www.ncbi.nlm.nih.gov/pubmed/28710399 http://dx.doi.org/10.1038/s41598-017-03887-3 |
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author | Bai, Xiaochen Tang, Yilin Yu, Mei Wu, Lei Liu, Fengtao Ni, Jianliang Wang, Zishan Wang, Jinghui Fei, Jian Wang, Wei Huang, Fang Wang, Jian |
author_facet | Bai, Xiaochen Tang, Yilin Yu, Mei Wu, Lei Liu, Fengtao Ni, Jianliang Wang, Zishan Wang, Jinghui Fei, Jian Wang, Wei Huang, Fang Wang, Jian |
author_sort | Bai, Xiaochen |
collection | PubMed |
description | There is currently no reliable and easily applicable diagnostic marker for Parkinson’s disease (PD). The aims of the present study were to compare the expression profiles of the microRNA29 family (miR-29s) in blood serum from patients with PD with healthy controls and to clarify whether the expression of miR-29s is correlated with disease severity, duration or L-dopa therapy and whether expression depends on the gender and age of patients. The levels of blood serum miR-29s in 80 patients with PD and 80 unaffected controls were assessed by reverse transcription-quantitative real-time PCR. The PCR products were confirmed by cloning and sequencing. Additionally, the expression of miR-7 in the blood serum from PD patients and control subjects was assessed. Serum miR-29 levels were significantly downregulated in PD patients compared to healthy controls. The serum miR-29 levels in female PD patients were markedly higher than in male PD patients. The expression of serum miR-29a and miR-29c expression tended to decrease with disease severity. Moreover, we found that serum miR-7 levels did not differ between PD patients and control subjects. Therefore, the reduction of serum miR-29 levels, particularly miR-29a and miR-29c, warrants further investigation of its potential serving as biomarkers for PD. |
format | Online Article Text |
id | pubmed-5511199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55111992017-07-17 Downregulation of blood serum microRNA 29 family in patients with Parkinson’s disease Bai, Xiaochen Tang, Yilin Yu, Mei Wu, Lei Liu, Fengtao Ni, Jianliang Wang, Zishan Wang, Jinghui Fei, Jian Wang, Wei Huang, Fang Wang, Jian Sci Rep Article There is currently no reliable and easily applicable diagnostic marker for Parkinson’s disease (PD). The aims of the present study were to compare the expression profiles of the microRNA29 family (miR-29s) in blood serum from patients with PD with healthy controls and to clarify whether the expression of miR-29s is correlated with disease severity, duration or L-dopa therapy and whether expression depends on the gender and age of patients. The levels of blood serum miR-29s in 80 patients with PD and 80 unaffected controls were assessed by reverse transcription-quantitative real-time PCR. The PCR products were confirmed by cloning and sequencing. Additionally, the expression of miR-7 in the blood serum from PD patients and control subjects was assessed. Serum miR-29 levels were significantly downregulated in PD patients compared to healthy controls. The serum miR-29 levels in female PD patients were markedly higher than in male PD patients. The expression of serum miR-29a and miR-29c expression tended to decrease with disease severity. Moreover, we found that serum miR-7 levels did not differ between PD patients and control subjects. Therefore, the reduction of serum miR-29 levels, particularly miR-29a and miR-29c, warrants further investigation of its potential serving as biomarkers for PD. Nature Publishing Group UK 2017-07-14 /pmc/articles/PMC5511199/ /pubmed/28710399 http://dx.doi.org/10.1038/s41598-017-03887-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bai, Xiaochen Tang, Yilin Yu, Mei Wu, Lei Liu, Fengtao Ni, Jianliang Wang, Zishan Wang, Jinghui Fei, Jian Wang, Wei Huang, Fang Wang, Jian Downregulation of blood serum microRNA 29 family in patients with Parkinson’s disease |
title | Downregulation of blood serum microRNA 29 family in patients with Parkinson’s disease |
title_full | Downregulation of blood serum microRNA 29 family in patients with Parkinson’s disease |
title_fullStr | Downregulation of blood serum microRNA 29 family in patients with Parkinson’s disease |
title_full_unstemmed | Downregulation of blood serum microRNA 29 family in patients with Parkinson’s disease |
title_short | Downregulation of blood serum microRNA 29 family in patients with Parkinson’s disease |
title_sort | downregulation of blood serum microrna 29 family in patients with parkinson’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511199/ https://www.ncbi.nlm.nih.gov/pubmed/28710399 http://dx.doi.org/10.1038/s41598-017-03887-3 |
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