3.8 Article

Nanoparticle-Based Modification of the DNA Methylome: A Therapeutic Tool for Atherosclerosis?

Journal

CARDIOGENETICS
Volume 12, Issue 1, Pages 12-23

Publisher

MDPI
DOI: 10.3390/cardiogenetics12010002

Keywords

atherosclerosis; bioactive molecule delivery; drug delivery; epigenetics; DNA methylation; nanoparticle

Funding

  1. Mexican National Council for Science and Technology (CONACyT) Atencion a Problemas Nacionales Programme [PDCPN-2015-01-584]
  2. CONACyT

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Cardiovascular epigenomics is a young field that provides new insights into gene regulation in atherosclerosis and offers new avenues for prevention and therapy. Advances in nanoparticle technology allow targeted delivery of drugs and bioactive molecules to the vascular wall. The partnership of these two fields has the potential to generate novel treatments for atherosclerosis.
Cardiovascular epigenomics is a relatively young field of research, yet it is providing novel insights into gene regulation in the atherosclerotic arterial wall. That information is already pointing to new avenues for atherosclerosis (AS) prevention and therapy. In parallel, advances in nanoparticle (NP) technology allow effective targeting of drugs and bioactive molecules to the vascular wall. The partnership of NP technology and epigenetics in AS is just beginning and promises to produce novel exciting candidate treatments. Here, we briefly discuss the most relevant recent advances in the two fields. We focus on AS and DNA methylation, as the DNA methylome of that condition is better understood in comparison with the rest of the cardiovascular disease field. In particular, we review the most recent advances in NP-based delivery systems and their use for DNA methylome modification in inflammation. We also address the promises of DNA methyltransferase inhibitors for prevention and therapy. Furthermore, we emphasize the unique challenges in designing therapies that target the cardiovascular epigenome. Lastly, we touch the issue of human exposure to industrial NPs and its impact on the epigenome as a reminder of the undesired effects that any NP-based therapy must avoid to be apt for secondary prevention of AS.

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