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PRMTs and miRNAs: functional cooperation in cancer and beyond.
- Source :
-
Cell cycle (Georgetown, Tex.) [Cell Cycle] 2019 Aug; Vol. 18 (15), pp. 1676-1686. Date of Electronic Publication: 2019 Jun 24. - Publication Year :
- 2019
-
Abstract
- Epigenetic modulators play pivotal roles in directing gene expression for the maintenance of normal cellular functions. However, when these modulators are aberrantly regulated, this can result in a variety of disease states, including cancer. One class of epigenetic regulators, protein arginine methyltransferases (PRMTs), have been shown to play critical roles in disease through methylation of arginine residues (R) on histone or non-histone proteins. Quite different from PRMTs, microRNAs (miRNAs) belong to the family of modulators known as noncoding RNAs (ncRNA) that act to regulate gene expression via RNA-mediated gene silencing. Importantly, miRNAs are frequently dysregulated and contribute to the progression of cancer and other conditions, including neurological and cardiovascular diseases. Recently, numerous studies have shown that miRNAs and other epigenetic enzymes can co-regulate each other. This review highlights multiple nodes of interaction between miRNAs and PRMTs and also discusses how this interplay might open up promising opportunities for drug development for the treatment of cancer and other diseases.
- Subjects :
- 3' Untranslated Regions
Arginine metabolism
Cardiovascular Diseases genetics
Cardiovascular Diseases metabolism
Cardiovascular Diseases therapy
Epigenesis, Genetic
Histones chemistry
Humans
Inflammation genetics
Inflammation metabolism
Inflammation therapy
Methylation
MicroRNAs biosynthesis
MicroRNAs genetics
Neoplasms metabolism
Neoplasms therapy
Neurodegenerative Diseases genetics
Neurodegenerative Diseases metabolism
Neurodegenerative Diseases therapy
Peptide Chain Initiation, Translational genetics
Protein Binding
Histones metabolism
MicroRNAs metabolism
Neoplasms genetics
Protein-Arginine N-Methyltransferases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1551-4005
- Volume :
- 18
- Issue :
- 15
- Database :
- MEDLINE
- Journal :
- Cell cycle (Georgetown, Tex.)
- Publication Type :
- Academic Journal
- Accession number :
- 31234694
- Full Text :
- https://doi.org/10.1080/15384101.2019.1629791