Epigenetics of Estrogen and Progesterone Receptors in Endometriosis

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This review discusses epigenetic mechanisms including DNA methylation, histone modification, miRNAs, and lncRNAs in regulating estrogen and progesterone receptor expression in endometriosis.

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This paper reviews evidence that epigenetic mechanisms regulate the expression of estrogen receptors (ERs) and progesterone receptors (PRs) in endometriosis, focusing on DNA methylation and histone modifications as well as non-classic mechanisms involving miRNAs and lncRNAs. Drawing on multiple in vitro and in vivo studies, it reports that epigenetic regulation of ER/PR expression can influence key disease-relevant hormonal pathways, including progesterone resistance and inflammatory responses. A limitation is that the review is not a single primary study and synthesizes heterogeneous findings across different models and targets, so causal mechanisms and effect sizes are not standardized. This paper is centrally about endometriosis — it specifically discusses how epigenetic control of estrogen and progesterone receptor expression may drive endometriosis pathology.

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Abstract

Endometriosis is an estrogen-dependent inflammatory gynecological disease. Increased estrogen activity and progesterone resistance are the main hormonal substrate of this disease and are associated with inflammatory response and debilitating symptoms, including pain and infertility. Estrogens and progesterone act via their specific nuclear receptors. The regulation of receptor expression by epigenetics maybe a critical factor for endometriosis. The present review aims to discuss the epigenetic mechanisms related to the expression of estrogen receptors (ERs) and progesterone receptors (PRs) in patients with endometriosis, including two classic epigenetic mechanisms: DNA methylation and histone modification, and, other non-classic mechanisms: miRNAs and lncRNA. Several in vitro and in vivo studies support the key role of epigenetics in the regulation of the expression of ERs and PRs, which may provide new molecules and targets for the diagnosis and treatment of endometriosis. Similar content being viewed by others

References

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Acknowledgments The study has been contributed with the support of “Fondazione Careggi-Academy for Women’s Health,” “Fondazione CR Firenze, project entitled The First 1000 Days of Life: Ambiental Disruptors and Women’s Health” endometriosis No.181010, the National Natural Science Foundation of China (81701401 to Luting Chen) and AHH and FP extend their appreciation to the International Scientific Partnership Program ISPP at King Saud University for funding this research work through ISPP# 152. Author information Authors and Affiliations Corresponding author Ethics declarations Conflict of Interest The authors declare that they have no conflict of interest. Ethics Approval Not applicable. Additional information Publisher’s Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Rights and permissions About this article Cite this article Chen, H., Malentacchi, F., Fambrini, M. et al. Epigenetics of Estrogen and Progesterone Receptors in Endometriosis. Reprod. Sci. 27, 1967–1974 (2020). https://doi.org/10.1007/s43032-020-00226-2 Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s43032-020-00226-2

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mesh:D004715endometriosis

MeSH descriptors

Endometriosis Epigenesis, Genetic Receptors, Estrogen Receptors, Progesterone DNA Methylation Endometriosis Female Gene Expression Regulation Humans MicroRNAs MicroRNAs Receptors, Estrogen Receptors, Progesterone RNA, Long Noncoding RNA, Long Noncoding

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