Differential Methylation Signatures Associated with PCOS- A Systematic Review and In-Silico Analysis.

IF 2.5 3区 医学 Q2 OBSTETRICS & GYNECOLOGY
Priya Sharma, Ahelee Ghosal, Aiswarya Vs, Shweta Daryani, Tulsi Brahma, Preeti Khetarpal
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引用次数: 0

Abstract

Polycystic ovary syndrome (PCOS) is a common endocrinopathy affecting 5-20% of reproductive-age women. Besides genetic factors, environmental triggers are considered major underlying causes that play a role through epigenetic alterations. Since epigenetic studies can be a possible link to explain the complexity of multifactorial disorders, it is worthwhile to investigate differentially methylated regions (DMRs) associated with PCOS. Therefore, a systematic review was conducted to identify epigenetic modifications associated with PCOS and analyse their functional role in the pathogenesis of the syndrome. After following inclusion and exclusion criteria, various databases (PubMed, Google Scholar, Central Cochrane Library, and Science Direct) were searched with predetermined keywords up to 30th June 2025, and quality of the selected articles assessed through the Newcastle Ottawa scale (NOS). In-silico analysis was performed by STRING, and Shiny GO. A total of 46 eligible studies were included, were further sub-categorized based on the sample type. A total of one hundred eleven genes were identified with altered DMRs, out of which thirty seven genes were reported from the ovarian tissues alone. Their GO analysis shows a significant interaction with other PCOS-susceptible genes and their functions in female sex differentiation and gonadal development. However, in-silico analysis of thirty six genes identified in blood showed their functions were significantly involved in the insulin-like growth factor binding activity. Gene enrichment analysis of fifteen genes with altered methylation identified in adipose tissue shows the significant involvement of female sex differentiation and insulin-activated receptor functions. Further, alterations in methylation of which genes (INSR, AMHR2, YAP1, CYP19A1, LHCGR, CDKN1A, LINE-1, AMH and TOX3) have been reported by at least two separate studies, irrespective of sample type. Their in-silico analysis shows significant involvement of these genes in the female sex characters, and gonadal development The current study highlights tissue-specific epigenetic modifications in PCOS, summarizes DMRs of genes which are involved in reproductive and insulin-related pathways. DMRs of identified genes may have a role in the pathogenesis of PCOS, insight into which may provide novel therapeutic targets in the future.

与PCOS相关的差异甲基化特征-系统回顾和计算机分析。
多囊卵巢综合征(PCOS)是一种常见的内分泌疾病,影响5-20%的育龄妇女。除了遗传因素外,环境因素被认为是通过表观遗传改变发挥作用的主要潜在原因。由于表观遗传学研究可能是解释多因子疾病复杂性的一个可能环节,因此研究与多囊卵巢综合征相关的差异甲基化区域(DMRs)是值得的。因此,我们进行了一项系统的综述,以确定与多囊卵巢综合征相关的表观遗传修饰,并分析它们在多囊卵巢综合征发病机制中的功能作用。在遵循纳入和排除标准后,使用预定的关键词检索到2025年6月30日之前的各种数据库(PubMed、谷歌Scholar、Central Cochrane Library和Science Direct),并通过纽卡斯尔渥太华量表(NOS)评估所选文章的质量。用STRING和Shiny GO进行芯片分析。共纳入46项符合条件的研究,并根据样本类型进一步分类。共有111个基因被鉴定为DMRs改变,其中37个基因仅来自卵巢组织。他们的氧化石墨烯分析显示,与其他多囊卵巢综合征易感基因及其在女性性别分化和性腺发育中的功能有显著的相互作用。然而,对血液中36个基因的计算机分析表明,它们的功能与胰岛素样生长因子的结合活性密切相关。在脂肪组织中鉴定的15个甲基化改变基因的基因富集分析表明,雌性性别分化和胰岛素激活受体功能的显著参与。此外,至少有两项独立的研究报告了这些基因(INSR、AMHR2、YAP1、CYP19A1、LHCGR、CDKN1A、LINE-1、AMH和TOX3)的甲基化改变,而不考虑样品类型。他们的计算机分析表明,这些基因在女性的性别特征和性腺发育中有重要的作用。目前的研究重点是多囊卵巢综合征的组织特异性表观遗传修饰,总结了参与生殖和胰岛素相关途径的基因的DMRs。已鉴定基因的DMRs可能在多囊卵巢综合征的发病机制中发挥作用,为今后提供新的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Reproductive Sciences
Reproductive Sciences 医学-妇产科学
CiteScore
5.50
自引率
3.40%
发文量
322
审稿时长
4-8 weeks
期刊介绍: Reproductive Sciences (RS) is a peer-reviewed, monthly journal publishing original research and reviews in obstetrics and gynecology. RS is multi-disciplinary and includes research in basic reproductive biology and medicine, maternal-fetal medicine, obstetrics, gynecology, reproductive endocrinology, urogynecology, fertility/infertility, embryology, gynecologic/reproductive oncology, developmental biology, stem cell research, molecular/cellular biology and other related fields.
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