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Epigenetic Modification Mechanisms Involved in Inflammation and Fibrosis in Renal Pathology.
- Source :
-
Mediators of inflammation [Mediators Inflamm] 2018 Dec 13; Vol. 2018, pp. 2931049. Date of Electronic Publication: 2018 Dec 13 (Print Publication: 2018). - Publication Year :
- 2018
-
Abstract
- 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.
- Subjects :
- Animals
DNA Methylation genetics
DNA Methylation physiology
Epigenesis, Genetic physiology
Fibrosis genetics
Histone Code genetics
Histone Code physiology
Humans
Kidney metabolism
Kidney pathology
Kidney Failure, Chronic
MicroRNAs
Renal Insufficiency, Chronic genetics
Epigenesis, Genetic genetics
Inflammation genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1466-1861
- Volume :
- 2018
- Database :
- MEDLINE
- Journal :
- Mediators of inflammation
- Publication Type :
- Academic Journal
- Accession number :
- 30647531
- Full Text :
- https://doi.org/10.1155/2018/2931049