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Prenatal circulating microRNA signatures of foetal Down syndrome
The altered expression pattern of miRNAs might potentially reflect anomalies related to foetal chromosomal aberrations. The aim of the study was to determine the expression level of miRNAs in plasma of pregnant women with foetal Down syndrome (DS). Out of 198 amniocentesis performed at 15–18 weeks o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382869/ https://www.ncbi.nlm.nih.gov/pubmed/30787377 http://dx.doi.org/10.1038/s41598-018-35876-5 |
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author | Zbucka-Kretowska, Monika Niemira, Magdalena Paczkowska-Abdulsalam, Magdalena Bielska, Agnieszka Szalkowska, Anna Parfieniuk, Ewa Ciborowski, Michal Wolczynski, Slawomir Kretowski, Adam |
author_facet | Zbucka-Kretowska, Monika Niemira, Magdalena Paczkowska-Abdulsalam, Magdalena Bielska, Agnieszka Szalkowska, Anna Parfieniuk, Ewa Ciborowski, Michal Wolczynski, Slawomir Kretowski, Adam |
author_sort | Zbucka-Kretowska, Monika |
collection | PubMed |
description | The altered expression pattern of miRNAs might potentially reflect anomalies related to foetal chromosomal aberrations. The aim of the study was to determine the expression level of miRNAs in plasma of pregnant women with foetal Down syndrome (DS). Out of 198 amniocentesis performed at 15–18 weeks of gestation, within a group of 12 patients with foetal DS and 12 patients with uncomplicated pregnancies, who delivered healthy newborns at term, we examined the expression level of 800 miRNAs using the NanoString technology. Our study revealed that there are 6 miRNAs were upregulated (hsa-miR-15a, hsa-let-7d, hsa-miR-142, hsa-miR-23a, hsa-miR-199, hsa-miR-191) and 7 were downregulated (hsa-miR-1290, hsa-miR-1915, hsa-miR30e, hsa-miR-1260, hsa-miR-483, hsa-miR-548, hsa-miR-590) in plasma samples of women with foetal DS syndrome. The genes regulated by identified miRNAs are involved in central nervous system development, congenital abnormalities and heart defects. The results of the present study yielded information on DS-specific miRNA expression signature, which can further help to design a panel of miRNAs as a non-invasive test for DS diagnosis. We believe that identified miRNAs may attend in the pathogenesis of DS and would potentially make a significant role for the future preventive therapies. |
format | Online Article Text |
id | pubmed-6382869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63828692019-02-25 Prenatal circulating microRNA signatures of foetal Down syndrome Zbucka-Kretowska, Monika Niemira, Magdalena Paczkowska-Abdulsalam, Magdalena Bielska, Agnieszka Szalkowska, Anna Parfieniuk, Ewa Ciborowski, Michal Wolczynski, Slawomir Kretowski, Adam Sci Rep Article The altered expression pattern of miRNAs might potentially reflect anomalies related to foetal chromosomal aberrations. The aim of the study was to determine the expression level of miRNAs in plasma of pregnant women with foetal Down syndrome (DS). Out of 198 amniocentesis performed at 15–18 weeks of gestation, within a group of 12 patients with foetal DS and 12 patients with uncomplicated pregnancies, who delivered healthy newborns at term, we examined the expression level of 800 miRNAs using the NanoString technology. Our study revealed that there are 6 miRNAs were upregulated (hsa-miR-15a, hsa-let-7d, hsa-miR-142, hsa-miR-23a, hsa-miR-199, hsa-miR-191) and 7 were downregulated (hsa-miR-1290, hsa-miR-1915, hsa-miR30e, hsa-miR-1260, hsa-miR-483, hsa-miR-548, hsa-miR-590) in plasma samples of women with foetal DS syndrome. The genes regulated by identified miRNAs are involved in central nervous system development, congenital abnormalities and heart defects. The results of the present study yielded information on DS-specific miRNA expression signature, which can further help to design a panel of miRNAs as a non-invasive test for DS diagnosis. We believe that identified miRNAs may attend in the pathogenesis of DS and would potentially make a significant role for the future preventive therapies. Nature Publishing Group UK 2019-02-20 /pmc/articles/PMC6382869/ /pubmed/30787377 http://dx.doi.org/10.1038/s41598-018-35876-5 Text en © The Author(s) 2019 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 Zbucka-Kretowska, Monika Niemira, Magdalena Paczkowska-Abdulsalam, Magdalena Bielska, Agnieszka Szalkowska, Anna Parfieniuk, Ewa Ciborowski, Michal Wolczynski, Slawomir Kretowski, Adam Prenatal circulating microRNA signatures of foetal Down syndrome |
title | Prenatal circulating microRNA signatures of foetal Down syndrome |
title_full | Prenatal circulating microRNA signatures of foetal Down syndrome |
title_fullStr | Prenatal circulating microRNA signatures of foetal Down syndrome |
title_full_unstemmed | Prenatal circulating microRNA signatures of foetal Down syndrome |
title_short | Prenatal circulating microRNA signatures of foetal Down syndrome |
title_sort | prenatal circulating microrna signatures of foetal down syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382869/ https://www.ncbi.nlm.nih.gov/pubmed/30787377 http://dx.doi.org/10.1038/s41598-018-35876-5 |
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