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Embryonic miRNA Profiles of Normal and Ectopic Pregnancies
Our objective was to investigate the miRNA profile of embryonic tissues in ectopic pregnancies (EPs) and controlled abortions (voluntary termination of pregnancy; VTOP). Twenty-three patients suffering from tubal EP and twenty-nine patients with a normal ongoing pregnancy scheduled for a VTOP were r...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094496/ https://www.ncbi.nlm.nih.gov/pubmed/25013942 http://dx.doi.org/10.1371/journal.pone.0102185 |
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author | Dominguez, Francisco Moreno-Moya, Juan Manuel Lozoya, Teresa Romero, Ainhoa Martínez, Sebastian Monterde, Mercedes Gurrea, Marta Ferri, Blanca Núñez, Maria Jose Simón, Carlos Pellicer, Antonio |
author_facet | Dominguez, Francisco Moreno-Moya, Juan Manuel Lozoya, Teresa Romero, Ainhoa Martínez, Sebastian Monterde, Mercedes Gurrea, Marta Ferri, Blanca Núñez, Maria Jose Simón, Carlos Pellicer, Antonio |
author_sort | Dominguez, Francisco |
collection | PubMed |
description | Our objective was to investigate the miRNA profile of embryonic tissues in ectopic pregnancies (EPs) and controlled abortions (voluntary termination of pregnancy; VTOP). Twenty-three patients suffering from tubal EP and twenty-nine patients with a normal ongoing pregnancy scheduled for a VTOP were recruited. Embryonic tissue samples were analyzed by miRNA microarray and further validated by real time PCR. Microarray studies showed that four miRNAs were differentially downregulated (hsa-mir-196b, hsa-mir-30a, hsa-mir-873, and hsa-mir-337-3p) and three upregulated (hsa-mir-1288, hsa-mir-451, and hsa-mir-223) in EP compared to control tissue samples. Hsa-miR-196, hsa-miR-223, and hsa-miR-451 were further validated by real time PCR in a wider population of EP and control samples. We also performed a computational analysis to identify the gene targets and pathways which might be modulated by these three differentially expressed miRNAs. The most significant pathways found were the mucin type O-glycan biosynthesis and the ECM-receptor-interaction pathways. We also checked that the dysregulation of these three miRNAs was able to alter the expression of the gene targets in the embryonic tissues included in these pathways such as GALNT13 and ITGA2 genes. In conclusion, analysis of miRNAs in ectopic and eutopic embryonic tissues shows different expression patterns that could modify pathways which are critical for correct implantation, providing new insights into the understanding of ectopic implantation in humans. |
format | Online Article Text |
id | pubmed-4094496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40944962014-07-15 Embryonic miRNA Profiles of Normal and Ectopic Pregnancies Dominguez, Francisco Moreno-Moya, Juan Manuel Lozoya, Teresa Romero, Ainhoa Martínez, Sebastian Monterde, Mercedes Gurrea, Marta Ferri, Blanca Núñez, Maria Jose Simón, Carlos Pellicer, Antonio PLoS One Research Article Our objective was to investigate the miRNA profile of embryonic tissues in ectopic pregnancies (EPs) and controlled abortions (voluntary termination of pregnancy; VTOP). Twenty-three patients suffering from tubal EP and twenty-nine patients with a normal ongoing pregnancy scheduled for a VTOP were recruited. Embryonic tissue samples were analyzed by miRNA microarray and further validated by real time PCR. Microarray studies showed that four miRNAs were differentially downregulated (hsa-mir-196b, hsa-mir-30a, hsa-mir-873, and hsa-mir-337-3p) and three upregulated (hsa-mir-1288, hsa-mir-451, and hsa-mir-223) in EP compared to control tissue samples. Hsa-miR-196, hsa-miR-223, and hsa-miR-451 were further validated by real time PCR in a wider population of EP and control samples. We also performed a computational analysis to identify the gene targets and pathways which might be modulated by these three differentially expressed miRNAs. The most significant pathways found were the mucin type O-glycan biosynthesis and the ECM-receptor-interaction pathways. We also checked that the dysregulation of these three miRNAs was able to alter the expression of the gene targets in the embryonic tissues included in these pathways such as GALNT13 and ITGA2 genes. In conclusion, analysis of miRNAs in ectopic and eutopic embryonic tissues shows different expression patterns that could modify pathways which are critical for correct implantation, providing new insights into the understanding of ectopic implantation in humans. Public Library of Science 2014-07-11 /pmc/articles/PMC4094496/ /pubmed/25013942 http://dx.doi.org/10.1371/journal.pone.0102185 Text en © 2014 Dominguez et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Dominguez, Francisco Moreno-Moya, Juan Manuel Lozoya, Teresa Romero, Ainhoa Martínez, Sebastian Monterde, Mercedes Gurrea, Marta Ferri, Blanca Núñez, Maria Jose Simón, Carlos Pellicer, Antonio Embryonic miRNA Profiles of Normal and Ectopic Pregnancies |
title | Embryonic miRNA Profiles of Normal and Ectopic Pregnancies |
title_full | Embryonic miRNA Profiles of Normal and Ectopic Pregnancies |
title_fullStr | Embryonic miRNA Profiles of Normal and Ectopic Pregnancies |
title_full_unstemmed | Embryonic miRNA Profiles of Normal and Ectopic Pregnancies |
title_short | Embryonic miRNA Profiles of Normal and Ectopic Pregnancies |
title_sort | embryonic mirna profiles of normal and ectopic pregnancies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094496/ https://www.ncbi.nlm.nih.gov/pubmed/25013942 http://dx.doi.org/10.1371/journal.pone.0102185 |
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