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Genome-wide microRNA expression profiling in placentae from frozen-thawed blastocyst transfer

BACKGROUND: Frozen-thawed embryo transfer (FET) is increasingly available for the improvement of the success rate of assisted reproductive technologies other than fresh embryo transfer (ET). There have been numerous findings that FET provides better obstetric and perinatal outcomes. However, the bir...

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Detalles Bibliográficos
Autores principales: Hiura, Hitoshi, Hattori, Hiromitsu, Kobayashi, Norio, Okae, Hiroaki, Chiba, Hatsune, Miyauchi, Naoko, Kitamura, Akane, Kikuchi, Hiroyuki, Yoshida, Hiroaki, Arima, Takahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543431/
https://www.ncbi.nlm.nih.gov/pubmed/28785370
http://dx.doi.org/10.1186/s13148-017-0379-6
Descripción
Sumario:BACKGROUND: Frozen-thawed embryo transfer (FET) is increasingly available for the improvement of the success rate of assisted reproductive technologies other than fresh embryo transfer (ET). There have been numerous findings that FET provides better obstetric and perinatal outcomes. However, the birth weight of infants conceived using FET is heavier than that of those conceived via ET. In addition, some reports have suggested that FET is associated with perinatal diseases such as placenta accreta and pregnancy-induced hypertension (PIH). RESULTS: In this study, we compared the microRNA (miRNA) expression profiles in term placentae derived from FET, ET, and spontaneous pregnancy (SP). We identified four miRNAs, miR-130a-3p, miR-149-5p, miR-423-5p, and miR-487b-3p, that were significantly downregulated in FET placentae compared with those from SP and ET. We found that DNA methylation of MEG3-DMR, not but IG-DMR, was associated with miRNA expression of the DLK1-DIO3 imprinted domain in the human placenta. In functional analyses, GO terms and signaling pathways related to positive regulation of gene expression, growth, development, cell migration, and type II diabetes mellitus (T2DM) were enriched. CONCLUSIONS: This study supports the hypothesis that the process of FET may increase exposure of epigenome to external influences. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-017-0379-6) contains supplementary material, which is available to authorized users.