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Identification of microRNAs and their target genes in the placenta as biomarkers of inflammation

OBJECTIVE: Recently, microRNA (miRNA) has been identified both as a powerful regulator involved in various biological processes through the regulation of numerous genes and as an effective biomarker for the prediction and diagnosis of various disease states. The objective of this study was to identi...

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Autores principales: Jang, Hee Yeon, Lim, Seung Mook, Lee, Hyun Jung, Hong, Joon-Seok, Kim, Gi Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Reproductive Medicine 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127901/
https://www.ncbi.nlm.nih.gov/pubmed/32146774
http://dx.doi.org/10.5653/cerm.2019.03013
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author Jang, Hee Yeon
Lim, Seung Mook
Lee, Hyun Jung
Hong, Joon-Seok
Kim, Gi Jin
author_facet Jang, Hee Yeon
Lim, Seung Mook
Lee, Hyun Jung
Hong, Joon-Seok
Kim, Gi Jin
author_sort Jang, Hee Yeon
collection PubMed
description OBJECTIVE: Recently, microRNA (miRNA) has been identified both as a powerful regulator involved in various biological processes through the regulation of numerous genes and as an effective biomarker for the prediction and diagnosis of various disease states. The objective of this study was to identify and validate miRNAs and their target genes involved in inflammation in placental tissue. METHODS: Microarrays were utilized to obtain miRNA and gene expression profiles from placentas with or without inflammation obtained from nine normal pregnant women and 10 preterm labor patients. Quantitative real-time polymerase chain reaction and Western blots were performed to validate the miRNAs and differentially-expressed genes in the placentas with inflammation. Correlations between miRNA and target gene expression were confirmed by luciferase assays in HTR-8/SVneo cells. RESULTS: We identified and validated miRNAs and their target genes that were differentially expressed in placentas with inflammation. We also demonstrated that several miRNAs (miR-371a-5p, miR-3065-3p, miR-519b-3p, and miR-373-3p) directly targeted their target genes (LEF1, LOX, ITGB4, and CD44). However, some miRNAs and their direct target genes showed no correlation in tissue samples. Interestingly, miR-373-3p and miR-3065-3p were markedly regulated by lipopolysaccharide (LPS) treatment, although the expression of their direct targets CD44 and LOX was not altered by LPS treatment. CONCLUSION: These results provide candidate miRNAs and their target genes that could be used as placental biomarkers of inflammation. These candidates may be useful for further miRNA-based biomarker development.
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spelling pubmed-71279012020-04-09 Identification of microRNAs and their target genes in the placenta as biomarkers of inflammation Jang, Hee Yeon Lim, Seung Mook Lee, Hyun Jung Hong, Joon-Seok Kim, Gi Jin Clin Exp Reprod Med Original Article OBJECTIVE: Recently, microRNA (miRNA) has been identified both as a powerful regulator involved in various biological processes through the regulation of numerous genes and as an effective biomarker for the prediction and diagnosis of various disease states. The objective of this study was to identify and validate miRNAs and their target genes involved in inflammation in placental tissue. METHODS: Microarrays were utilized to obtain miRNA and gene expression profiles from placentas with or without inflammation obtained from nine normal pregnant women and 10 preterm labor patients. Quantitative real-time polymerase chain reaction and Western blots were performed to validate the miRNAs and differentially-expressed genes in the placentas with inflammation. Correlations between miRNA and target gene expression were confirmed by luciferase assays in HTR-8/SVneo cells. RESULTS: We identified and validated miRNAs and their target genes that were differentially expressed in placentas with inflammation. We also demonstrated that several miRNAs (miR-371a-5p, miR-3065-3p, miR-519b-3p, and miR-373-3p) directly targeted their target genes (LEF1, LOX, ITGB4, and CD44). However, some miRNAs and their direct target genes showed no correlation in tissue samples. Interestingly, miR-373-3p and miR-3065-3p were markedly regulated by lipopolysaccharide (LPS) treatment, although the expression of their direct targets CD44 and LOX was not altered by LPS treatment. CONCLUSION: These results provide candidate miRNAs and their target genes that could be used as placental biomarkers of inflammation. These candidates may be useful for further miRNA-based biomarker development. Korean Society for Reproductive Medicine 2020-03 2020-03-01 /pmc/articles/PMC7127901/ /pubmed/32146774 http://dx.doi.org/10.5653/cerm.2019.03013 Text en Copyright © 2020. THE KOREAN SOCIETY FOR REPRODUCTIVE MEDICINE This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jang, Hee Yeon
Lim, Seung Mook
Lee, Hyun Jung
Hong, Joon-Seok
Kim, Gi Jin
Identification of microRNAs and their target genes in the placenta as biomarkers of inflammation
title Identification of microRNAs and their target genes in the placenta as biomarkers of inflammation
title_full Identification of microRNAs and their target genes in the placenta as biomarkers of inflammation
title_fullStr Identification of microRNAs and their target genes in the placenta as biomarkers of inflammation
title_full_unstemmed Identification of microRNAs and their target genes in the placenta as biomarkers of inflammation
title_short Identification of microRNAs and their target genes in the placenta as biomarkers of inflammation
title_sort identification of micrornas and their target genes in the placenta as biomarkers of inflammation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127901/
https://www.ncbi.nlm.nih.gov/pubmed/32146774
http://dx.doi.org/10.5653/cerm.2019.03013
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