| Literature DB >> 31234694 |
Jiamin Jin1,2, Matthew Martin2, Antja-Voy Hartley2, Tao Lu2,3,4.
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.Entities:
Keywords: Cancer; PRMTs; disease; miRNA
Year: 2019 PMID: 31234694 PMCID: PMC6650030 DOI: 10.1080/15384101.2019.1629791
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534