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Non-coding RNAs in polycystic ovary syndrome: a systematic review and meta-analysis

BACKGROUND: Genetic, environmental and epigenetical factors may play important roles in the pathogenesis of polycystic ovary syndrome (PCOS), however the etiology of PCOS remains unclear. Studies indicated that non-coding RNAs (ncRNAs) were involved in the occurrence and development of PCOS. Thus, w...

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Autores principales: Mu, Liangshan, Sun, Xiaoting, Tu, Mixue, Zhang, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807442/
https://www.ncbi.nlm.nih.gov/pubmed/33446212
http://dx.doi.org/10.1186/s12958-020-00687-9
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author Mu, Liangshan
Sun, Xiaoting
Tu, Mixue
Zhang, Dan
author_facet Mu, Liangshan
Sun, Xiaoting
Tu, Mixue
Zhang, Dan
author_sort Mu, Liangshan
collection PubMed
description BACKGROUND: Genetic, environmental and epigenetical factors may play important roles in the pathogenesis of polycystic ovary syndrome (PCOS), however the etiology of PCOS remains unclear. Studies indicated that non-coding RNAs (ncRNAs) were involved in the occurrence and development of PCOS. Thus, we aim to perform a systematic review and meta-analysis to investigate the presence and dysregulated expression of ncRNAs in human PCOS. METHODS: We searched in PubMed, Medline, Web of Science and Embase until July 2019 and summarized all eligible publications focusing on microRNAs (miRNAs), long non-coding RNAs (lncRNAs), circular RNAs (circRNAs) and small interfering RNAs (siRNAs) in PCOS. RESULTS: Sixty-seven articles were included in our systematic review and 9 articles were included in meta-analysis. There is little overlap between studies when comparing miRNA profiles. Sensitivity analysis showed that the expression of miR-93 was upregulated in PCOS patients (WMD 0.75, P < 0.00001), without heterogeneity among remaining studies (I(2) = 0%). CONCLUSION: A large number of ncRNAs with altered levels were observed in plasma, serum, follicular fluid, granulosa cells or other issues from PCOS patients. Aberrant ncRNAs expression in PCOS may lead to aberrant steroidogenesis, adipocyte dysfunction, altered ovarian cell proliferation and/or apoptosis and have the potential to be used as diagnostic biomarkers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12958-020-00687-9.
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spelling pubmed-78074422021-01-14 Non-coding RNAs in polycystic ovary syndrome: a systematic review and meta-analysis Mu, Liangshan Sun, Xiaoting Tu, Mixue Zhang, Dan Reprod Biol Endocrinol Review BACKGROUND: Genetic, environmental and epigenetical factors may play important roles in the pathogenesis of polycystic ovary syndrome (PCOS), however the etiology of PCOS remains unclear. Studies indicated that non-coding RNAs (ncRNAs) were involved in the occurrence and development of PCOS. Thus, we aim to perform a systematic review and meta-analysis to investigate the presence and dysregulated expression of ncRNAs in human PCOS. METHODS: We searched in PubMed, Medline, Web of Science and Embase until July 2019 and summarized all eligible publications focusing on microRNAs (miRNAs), long non-coding RNAs (lncRNAs), circular RNAs (circRNAs) and small interfering RNAs (siRNAs) in PCOS. RESULTS: Sixty-seven articles were included in our systematic review and 9 articles were included in meta-analysis. There is little overlap between studies when comparing miRNA profiles. Sensitivity analysis showed that the expression of miR-93 was upregulated in PCOS patients (WMD 0.75, P < 0.00001), without heterogeneity among remaining studies (I(2) = 0%). CONCLUSION: A large number of ncRNAs with altered levels were observed in plasma, serum, follicular fluid, granulosa cells or other issues from PCOS patients. Aberrant ncRNAs expression in PCOS may lead to aberrant steroidogenesis, adipocyte dysfunction, altered ovarian cell proliferation and/or apoptosis and have the potential to be used as diagnostic biomarkers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12958-020-00687-9. BioMed Central 2021-01-14 /pmc/articles/PMC7807442/ /pubmed/33446212 http://dx.doi.org/10.1186/s12958-020-00687-9 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Mu, Liangshan
Sun, Xiaoting
Tu, Mixue
Zhang, Dan
Non-coding RNAs in polycystic ovary syndrome: a systematic review and meta-analysis
title Non-coding RNAs in polycystic ovary syndrome: a systematic review and meta-analysis
title_full Non-coding RNAs in polycystic ovary syndrome: a systematic review and meta-analysis
title_fullStr Non-coding RNAs in polycystic ovary syndrome: a systematic review and meta-analysis
title_full_unstemmed Non-coding RNAs in polycystic ovary syndrome: a systematic review and meta-analysis
title_short Non-coding RNAs in polycystic ovary syndrome: a systematic review and meta-analysis
title_sort non-coding rnas in polycystic ovary syndrome: a systematic review and meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807442/
https://www.ncbi.nlm.nih.gov/pubmed/33446212
http://dx.doi.org/10.1186/s12958-020-00687-9
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