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常染色体显性多囊肾病中的表观遗传学

Epigenetics in autosomal dominant polycystic kidney disease.

作者信息

Yan Zhipeng, Cao Feng, Shao Tingting, Liao Bingqing, Wang Guoping, Tang Xianhu, Luo Hongwen, Zhu Fengjuan, Liao Yunqiang, Zhang Fengxia, Li Xiaosheng, Wang Jian, Liu Zhenzhen, Zhuang Shougang

机构信息

Department of Nephrology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China; Department of Nephrology, the First Affiliated Hospital of Gannan Medical University, China.

Department of Nephrology, the First Affiliated Hospital of Gannan Medical University, China.

出版信息

Biochim Biophys Acta Mol Basis Dis. 2025 Mar;1871(3):167652. doi: 10.1016/j.bbadis.2024.167652. Epub 2025 Jan 1.

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is the fourth leading cause of end-stage renal disease, contributing substantially to patient morbidity, mortality, and healthcare system strain. Emerging research highlights a pivotal role of epigenetics in ADPKD's pathophysiology, where mechanisms like DNA methylation, histone modifications, and non-coding RNA regulation significantly impact disease onset and progression. These epigenetic factors influence gene expression and regulate key processes involved in cyst formation and expansion, fibrosis, and inflammatory infiltration, thus accelerating ADPKD progression. Consequently, exploring epigenetic regulatory mechanisms presents a valuable pathway for developing novel therapeutic strategies and diagnostic biomarkers aimed at slowing or preventing ADPKD progression. This review systematically examines existing studies on epigenetic alterations-including DNA methylation, histone modification, and non-coding RNA regulation-in ADPKD patients, providing insights into gene expression changes and functions, and identifying potential drug targets for ADPKD treatment. CLINICAL SIGNIFICANCE: Autosomal dominant polycystic kidney disease (ADPKD) is the fourth leading cause of end-stage renal disease, causing significant morbidity, increasing patient mortality, and weakening the healthcare system. Further study on ADPKD has revealed that epigenetics plays an important role in the pathophysiological process of ADPKD. Epigenetics has a significant impact on the formation and progression of ADPKD through a variety of processes including DNA methylation, histone modification, and non-coding RNA. In addition to boosting cyst formation and proliferation, it induces cystic fibrosis and inflammatory cell infiltration, ultimately leading to a poor prognosis. This review summarizes the current understanding of the associated alterations in gene expression and function produced by epigenetic regulation in ADPKD, as well as potential treatment targets.

摘要

常染色体显性多囊肾病(ADPKD)是终末期肾病的第四大主要病因,对患者的发病率、死亡率及医疗系统造成了巨大压力。新兴研究突显了表观遗传学在ADPKD病理生理学中的关键作用,其中DNA甲基化、组蛋白修饰及非编码RNA调控等机制对疾病的发生和进展有显著影响。这些表观遗传因素影响基因表达,并调控囊肿形成与扩张、纤维化及炎症浸润等关键过程,从而加速ADPKD的进展。因此,探索表观遗传调控机制为开发旨在延缓或预防ADPKD进展的新型治疗策略和诊断生物标志物提供了一条有价值的途径。本综述系统地审视了关于ADPKD患者表观遗传改变(包括DNA甲基化、组蛋白修饰及非编码RNA调控)的现有研究,深入了解基因表达变化及其功能,并确定ADPKD治疗的潜在药物靶点。临床意义:常染色体显性多囊肾病(ADPKD)是终末期肾病的第四大主要病因,导致严重的发病情况,增加患者死亡率,并削弱医疗系统。对ADPKD的进一步研究表明,表观遗传学在ADPKD的病理生理过程中发挥重要作用。表观遗传学通过DNA甲基化、组蛋白修饰及非编码RNA等多种过程对ADPKD的形成和进展产生重大影响。除了促进囊肿形成和增殖外,它还引发囊性纤维化和炎症细胞浸润,最终导致预后不良。本综述总结了目前对ADPKD中表观遗传调控所产生的相关基因表达和功能改变的理解,以及潜在的治疗靶点。

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