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Circulating microRNAs in follicular fluid, powerful tools to explore in vitro fertilization process

Circulating or “extracellular” microRNAs (miRNAs) detected in biological fluids, could be used as potential diagnostic and prognostic biomarkers of several disease, such as cancer, gynecological and pregnancy disorders. However, their contributions in female infertility and in vitro fertilization (I...

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Detalles Bibliográficos
Autores principales: Scalici, E., Traver, S., Mullet, T., Molinari, N., Ferrières, A., Brunet, C., Belloc, S., Hamamah, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840336/
https://www.ncbi.nlm.nih.gov/pubmed/27102646
http://dx.doi.org/10.1038/srep24976
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author Scalici, E.
Traver, S.
Mullet, T.
Molinari, N.
Ferrières, A.
Brunet, C.
Belloc, S.
Hamamah, S.
author_facet Scalici, E.
Traver, S.
Mullet, T.
Molinari, N.
Ferrières, A.
Brunet, C.
Belloc, S.
Hamamah, S.
author_sort Scalici, E.
collection PubMed
description Circulating or “extracellular” microRNAs (miRNAs) detected in biological fluids, could be used as potential diagnostic and prognostic biomarkers of several disease, such as cancer, gynecological and pregnancy disorders. However, their contributions in female infertility and in vitro fertilization (IVF) remain unknown. This study investigated the expression profiles of five circulating miRNAs (let-7b, miR-29a, miR-30a, miR-140 and miR-320a) in human follicular fluid from 91 women with normal ovarian reserve and 30 with polycystic ovary syndrome (PCOS) and their ability to predict IVF outcomes. The combination of FF miR-30a, miR-140 and let-7b expression levels discriminated between PCOS and normal ovarian reserve with a specificity of 83.8% and a sensitivity of 70% (area under the ROC curve, AUC = 0.83 [0.73–0.92]; p < 0.0001). FF samples related to low number of mature oocytes (≤2) contained significant less miR-320a levels than those related to a number of mature oocytes >2 (p = 0.04). Moreover, FF let-7b predicted the development of expanded blastocysts with 70% sensitivity and 64.3% specificity (AUC = 0.67 [0.54–0.79]; p = 0.02) and FF miR-29a potential to predict clinical pregnancy outcome reached 0.68 [0.55–0.79] with a sensitivity of 83.3% and a specificity of 53.5% (p = 0.01). Therefore, these miRNAs could provide new helpful biomarkers to facilitate personalized medical care during IVF.
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spelling pubmed-48403362016-04-28 Circulating microRNAs in follicular fluid, powerful tools to explore in vitro fertilization process Scalici, E. Traver, S. Mullet, T. Molinari, N. Ferrières, A. Brunet, C. Belloc, S. Hamamah, S. Sci Rep Article Circulating or “extracellular” microRNAs (miRNAs) detected in biological fluids, could be used as potential diagnostic and prognostic biomarkers of several disease, such as cancer, gynecological and pregnancy disorders. However, their contributions in female infertility and in vitro fertilization (IVF) remain unknown. This study investigated the expression profiles of five circulating miRNAs (let-7b, miR-29a, miR-30a, miR-140 and miR-320a) in human follicular fluid from 91 women with normal ovarian reserve and 30 with polycystic ovary syndrome (PCOS) and their ability to predict IVF outcomes. The combination of FF miR-30a, miR-140 and let-7b expression levels discriminated between PCOS and normal ovarian reserve with a specificity of 83.8% and a sensitivity of 70% (area under the ROC curve, AUC = 0.83 [0.73–0.92]; p < 0.0001). FF samples related to low number of mature oocytes (≤2) contained significant less miR-320a levels than those related to a number of mature oocytes >2 (p = 0.04). Moreover, FF let-7b predicted the development of expanded blastocysts with 70% sensitivity and 64.3% specificity (AUC = 0.67 [0.54–0.79]; p = 0.02) and FF miR-29a potential to predict clinical pregnancy outcome reached 0.68 [0.55–0.79] with a sensitivity of 83.3% and a specificity of 53.5% (p = 0.01). Therefore, these miRNAs could provide new helpful biomarkers to facilitate personalized medical care during IVF. Nature Publishing Group 2016-04-22 /pmc/articles/PMC4840336/ /pubmed/27102646 http://dx.doi.org/10.1038/srep24976 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Scalici, E.
Traver, S.
Mullet, T.
Molinari, N.
Ferrières, A.
Brunet, C.
Belloc, S.
Hamamah, S.
Circulating microRNAs in follicular fluid, powerful tools to explore in vitro fertilization process
title Circulating microRNAs in follicular fluid, powerful tools to explore in vitro fertilization process
title_full Circulating microRNAs in follicular fluid, powerful tools to explore in vitro fertilization process
title_fullStr Circulating microRNAs in follicular fluid, powerful tools to explore in vitro fertilization process
title_full_unstemmed Circulating microRNAs in follicular fluid, powerful tools to explore in vitro fertilization process
title_short Circulating microRNAs in follicular fluid, powerful tools to explore in vitro fertilization process
title_sort circulating micrornas in follicular fluid, powerful tools to explore in vitro fertilization process
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840336/
https://www.ncbi.nlm.nih.gov/pubmed/27102646
http://dx.doi.org/10.1038/srep24976
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