Cellular Biology in Renal Diseases Laboratory, Universidad Autónoma Madrid, IIS-Fundación Jiménez Díaz, Madrid, Spain.
RedInRen RETIC, ISCIII, Spain.
Mediators Inflamm. 2018 Dec 13;2018:2931049. doi: 10.1155/2018/2931049. eCollection 2018.
The growing incidence of obesity, hypertension, and diabetes, coupled with the aging of the population, is increasing the prevalence of renal diseases in our society. Chronic kidney disease (CKD) is characterized by persistent inflammation, fibrosis, and loss of renal function leading to end-stage renal disease. Nowadays, CKD treatment has limited effectiveness underscoring the importance of the development of innovative therapeutic options. Recent studies have identified how epigenetic modifications participate in the susceptibility to CKD and have explained how the environment interacts with the renal cell epigenome to contribute to renal damage. Epigenetic mechanisms regulate critical processes involved in gene regulation and downstream cellular responses. The most relevant epigenetic modifications that play a critical role in renal damage include DNA methylation, histone modifications, and changes in miRNA levels. Importantly, these epigenetic modifications are reversible and, therefore, a source of potential therapeutic targets. Here, we will explain how epigenetic mechanisms may regulate essential processes involved in renal pathology and highlight some possible epigenetic therapeutic strategies for CKD treatment.
肥胖症、高血压和糖尿病的发病率不断上升,加上人口老龄化,导致我们社会的肾脏疾病患病率不断上升。慢性肾脏病(CKD)的特征是持续的炎症、纤维化和肾功能丧失,导致终末期肾病。如今,CKD 的治疗效果有限,这凸显了开发创新治疗选择的重要性。最近的研究已经确定了表观遗传修饰如何参与 CKD 的易感性,并解释了环境如何与肾细胞表观基因组相互作用导致肾脏损伤。表观遗传机制调节参与基因调控和下游细胞反应的关键过程。在肾脏损伤中起关键作用的最相关的表观遗传修饰包括 DNA 甲基化、组蛋白修饰和 miRNA 水平的变化。重要的是,这些表观遗传修饰是可逆的,因此是潜在治疗靶点的来源。在这里,我们将解释表观遗传机制如何调节肾脏病理学中涉及的基本过程,并强调一些用于 CKD 治疗的潜在表观遗传治疗策略。