The role of DNA methylation in placental development and its implications for preeclampsia

Preeclampsia (PE) is a prevalent and multifaceted pregnancy disorder, characterized by high blood pressure, edema, proteinuria, and systemic organ dysfunction. It remains one of the leading causes of pregnancy complications, yet its exact origins and pathophysiological mechanisms are not fully under...

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Main Authors: Yizi Meng, Yimei Meng, Linli Li, Yuan Li, Jin He, Yanhong Shan
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-12-01
Series:Frontiers in Cell and Developmental Biology
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Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2024.1494072/full
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author Yizi Meng
Yimei Meng
Linli Li
Yuan Li
Jin He
Yanhong Shan
author_facet Yizi Meng
Yimei Meng
Linli Li
Yuan Li
Jin He
Yanhong Shan
author_sort Yizi Meng
collection DOAJ
description Preeclampsia (PE) is a prevalent and multifaceted pregnancy disorder, characterized by high blood pressure, edema, proteinuria, and systemic organ dysfunction. It remains one of the leading causes of pregnancy complications, yet its exact origins and pathophysiological mechanisms are not fully understood. Currently, the only definitive treatment is delivery, often requiring preterm termination of pregnancy, which increases neonatal and maternal morbidity and mortality rates, particularly in severe cases. This highlights the urgent need for further research to elucidate its underlying mechanisms and develop targeted interventions. PE is thought to result from a combination of factors, including inflammatory cytokines, trophoblast dysfunction, and environmental influences, which may trigger epigenetic changes, particularly DNA methylation. The placenta, a vital organ for fetal and maternal exchange, plays a central role in the onset of PE. Increasing evidence suggests a strong association between DNA methylation, placental function, and the development of PE. This review focuses on the impact of DNA methylation on placental development and its contribution to PE pathophysiology. It aims to clarify the epigenetic processes essential for normal placental development and explore potential epigenetic biomarkers and therapeutic targets for PE. Such insights could lead to the development of novel preventive and therapeutic strategies for this condition.
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spelling doaj-art-13b5628ff01c485e8fb56e1655965bb82024-12-03T06:30:29ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2024-12-011210.3389/fcell.2024.14940721494072The role of DNA methylation in placental development and its implications for preeclampsiaYizi Meng0Yimei Meng1Linli Li2Yuan Li3Jin He4Yanhong Shan5Department of Obstetrics, Obstetrics and Gynecology Center, The First Hospital of Jilin University, Changchun, ChinaDepartment of Obstetrics and Gynecology, The Second Affiliated Hospital of Harbin Medical University, Harbin, ChinaDepartment of Obstetrics, Obstetrics and Gynecology Center, The First Hospital of Jilin University, Changchun, ChinaDepartment of General Gynecology I, Obstetrics and Gynecology Center, The First Hospital of Jilin University, Changchun, ChinaDepartment of Obstetrics, Obstetrics and Gynecology Center, The First Hospital of Jilin University, Changchun, ChinaDepartment of Obstetrics, Obstetrics and Gynecology Center, The First Hospital of Jilin University, Changchun, ChinaPreeclampsia (PE) is a prevalent and multifaceted pregnancy disorder, characterized by high blood pressure, edema, proteinuria, and systemic organ dysfunction. It remains one of the leading causes of pregnancy complications, yet its exact origins and pathophysiological mechanisms are not fully understood. Currently, the only definitive treatment is delivery, often requiring preterm termination of pregnancy, which increases neonatal and maternal morbidity and mortality rates, particularly in severe cases. This highlights the urgent need for further research to elucidate its underlying mechanisms and develop targeted interventions. PE is thought to result from a combination of factors, including inflammatory cytokines, trophoblast dysfunction, and environmental influences, which may trigger epigenetic changes, particularly DNA methylation. The placenta, a vital organ for fetal and maternal exchange, plays a central role in the onset of PE. Increasing evidence suggests a strong association between DNA methylation, placental function, and the development of PE. This review focuses on the impact of DNA methylation on placental development and its contribution to PE pathophysiology. It aims to clarify the epigenetic processes essential for normal placental development and explore potential epigenetic biomarkers and therapeutic targets for PE. Such insights could lead to the development of novel preventive and therapeutic strategies for this condition.https://www.frontiersin.org/articles/10.3389/fcell.2024.1494072/fullpreeclampsiaDNA methylationplacental developmentepigenetic biomarkerstherapeutic targets
spellingShingle Yizi Meng
Yimei Meng
Linli Li
Yuan Li
Jin He
Yanhong Shan
The role of DNA methylation in placental development and its implications for preeclampsia
Frontiers in Cell and Developmental Biology
preeclampsia
DNA methylation
placental development
epigenetic biomarkers
therapeutic targets
title The role of DNA methylation in placental development and its implications for preeclampsia
title_full The role of DNA methylation in placental development and its implications for preeclampsia
title_fullStr The role of DNA methylation in placental development and its implications for preeclampsia
title_full_unstemmed The role of DNA methylation in placental development and its implications for preeclampsia
title_short The role of DNA methylation in placental development and its implications for preeclampsia
title_sort role of dna methylation in placental development and its implications for preeclampsia
topic preeclampsia
DNA methylation
placental development
epigenetic biomarkers
therapeutic targets
url https://www.frontiersin.org/articles/10.3389/fcell.2024.1494072/full
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