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Reduced microRNA-451 expression in eutopic endometrium contributes to the pathogenesis of endometriosis
BACKGROUND: Endometriosis (EMs) is a chronic and recurrent, but benign, disease in women of reproductive age, and EMs patients have a high risk of developing gynecological tumors and autoimmune disorders. The etiology of EMs is not clear. Certain genetic markers in the eutopic endometrium are key in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718782/ https://www.ncbi.nlm.nih.gov/pubmed/31531311 http://dx.doi.org/10.12998/wjcc.v7.i16.2155 |
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author | Gao, Shan Liu, Shuang Gao, Zi-Ming Deng, Peng Wang, Dan-Bo |
author_facet | Gao, Shan Liu, Shuang Gao, Zi-Ming Deng, Peng Wang, Dan-Bo |
author_sort | Gao, Shan |
collection | PubMed |
description | BACKGROUND: Endometriosis (EMs) is a chronic and recurrent, but benign, disease in women of reproductive age, and EMs patients have a high risk of developing gynecological tumors and autoimmune disorders. The etiology of EMs is not clear. Certain genetic markers in the eutopic endometrium are key in the pathogenesis of EMs. MicroRNAs (miRNAs) are implicated in several biological processes, such as cell proliferation, differentiation, and apoptosis. MiR-451 is interesting, as it acts as a tumor suppressor and is relevant to the poor prognosis of cancers. AIM: To evaluate the expression levels and role of miR-451 in the eutopic endometrium and predict possible targets of miR-451 and related signaling pathways. METHODS: Quantitative real-time polymerase chain reaction was used to evaluate miR-451 expression in cultured cell lines as well as in pathologic tissues from 40 patients with EMs and 20 donors with no history of the disease (controls). Cell Counting Kit-8 and flow cytometric assays were performed to determine cell proliferation and survival rates after transfection with miR-451 mimics and siRNAs. MiR-451 targets were predicted using miRDB and miRcode target-predicting databases. RESULTS: We observed lower miR-451 levels in eutopic endometrial tissues from patients with EMs than in control tissues, and this difference was not related to the American Society for Reproductive Medicine stage. Ectopic overexpression of miR-451 in eutopic cells induced apoptosis and inhibited cell proliferation. SiRNA-mediated miR-451 knockdown reversed these effects. Using miRDB and miRcode, we identified 12 potential miR-451 target genes. We hypothesize that the expression of YWHAZ, OSR1, TTN, and CDKN2D may be regulated by miR-451 and be involved in disease pathogenesis. CONCLUSION: Reduced miR-451 expression in the eutopic endometrium contributes to the pathogenesis of EMs by promoting cell proliferation and reducing apoptosis. Thus, miR-451 is a novel biomarker for EMs. YWHAZ, OSR1, TTN, and CDKN2D are potential target genes of miR-451 and may have key roles in this disease. |
format | Online Article Text |
id | pubmed-6718782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-67187822019-09-17 Reduced microRNA-451 expression in eutopic endometrium contributes to the pathogenesis of endometriosis Gao, Shan Liu, Shuang Gao, Zi-Ming Deng, Peng Wang, Dan-Bo World J Clin Cases Basic Study BACKGROUND: Endometriosis (EMs) is a chronic and recurrent, but benign, disease in women of reproductive age, and EMs patients have a high risk of developing gynecological tumors and autoimmune disorders. The etiology of EMs is not clear. Certain genetic markers in the eutopic endometrium are key in the pathogenesis of EMs. MicroRNAs (miRNAs) are implicated in several biological processes, such as cell proliferation, differentiation, and apoptosis. MiR-451 is interesting, as it acts as a tumor suppressor and is relevant to the poor prognosis of cancers. AIM: To evaluate the expression levels and role of miR-451 in the eutopic endometrium and predict possible targets of miR-451 and related signaling pathways. METHODS: Quantitative real-time polymerase chain reaction was used to evaluate miR-451 expression in cultured cell lines as well as in pathologic tissues from 40 patients with EMs and 20 donors with no history of the disease (controls). Cell Counting Kit-8 and flow cytometric assays were performed to determine cell proliferation and survival rates after transfection with miR-451 mimics and siRNAs. MiR-451 targets were predicted using miRDB and miRcode target-predicting databases. RESULTS: We observed lower miR-451 levels in eutopic endometrial tissues from patients with EMs than in control tissues, and this difference was not related to the American Society for Reproductive Medicine stage. Ectopic overexpression of miR-451 in eutopic cells induced apoptosis and inhibited cell proliferation. SiRNA-mediated miR-451 knockdown reversed these effects. Using miRDB and miRcode, we identified 12 potential miR-451 target genes. We hypothesize that the expression of YWHAZ, OSR1, TTN, and CDKN2D may be regulated by miR-451 and be involved in disease pathogenesis. CONCLUSION: Reduced miR-451 expression in the eutopic endometrium contributes to the pathogenesis of EMs by promoting cell proliferation and reducing apoptosis. Thus, miR-451 is a novel biomarker for EMs. YWHAZ, OSR1, TTN, and CDKN2D are potential target genes of miR-451 and may have key roles in this disease. Baishideng Publishing Group Inc 2019-08-26 2019-08-26 /pmc/articles/PMC6718782/ /pubmed/31531311 http://dx.doi.org/10.12998/wjcc.v7.i16.2155 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Basic Study Gao, Shan Liu, Shuang Gao, Zi-Ming Deng, Peng Wang, Dan-Bo Reduced microRNA-451 expression in eutopic endometrium contributes to the pathogenesis of endometriosis |
title | Reduced microRNA-451 expression in eutopic endometrium contributes to the pathogenesis of endometriosis |
title_full | Reduced microRNA-451 expression in eutopic endometrium contributes to the pathogenesis of endometriosis |
title_fullStr | Reduced microRNA-451 expression in eutopic endometrium contributes to the pathogenesis of endometriosis |
title_full_unstemmed | Reduced microRNA-451 expression in eutopic endometrium contributes to the pathogenesis of endometriosis |
title_short | Reduced microRNA-451 expression in eutopic endometrium contributes to the pathogenesis of endometriosis |
title_sort | reduced microrna-451 expression in eutopic endometrium contributes to the pathogenesis of endometriosis |
topic | Basic Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718782/ https://www.ncbi.nlm.nih.gov/pubmed/31531311 http://dx.doi.org/10.12998/wjcc.v7.i16.2155 |
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