| Literature DB >> 26949823 |
Silvia M Sirchia1, Alice Faversani2, Davide Rovina1, Maria V Russo2, Leda Paganini2,3, Federica Savi2, Claudia Augello2,3, Lorenzo Rosso4, Alessandro Del Gobbo2, Silvia Tabano2,3, Silvano Bosari2,3, Monica Miozzo2,3.
Abstract
BACKGROUND: Tumor epigenetic defects are of increasing relevance to clinical practice, because they are 'druggable' targets for cancer therapy using chromatin-remodeling agents (CRAs). New evidences highlight the importance of the microenvironment on the epigenome regulation and the need to use culture models able to preserve tissue morphology, to better understand the action of CRAs. Methods & methods: We studied the epigenetic response induced by culturing and CRAs in a preclinical model, preserving ex vivo the original tissue microenvironment and morphology, assessing different epigenetic signatures. Our overall findings suggest that culturing and CRAs cause heterogeneous effects on the genes methylation; CRAs affect the global DNA methylation and can trigger an active DNA demethylation; the culture induces alterations in the histone deacetylase expression.Entities:
Keywords: DNA hydroxymethylation; DNA methylation; HDAC; chromatin remodeling agents; epigenetics; organotypic culture
Mesh:
Substances:
Year: 2016 PMID: 26949823 DOI: 10.2217/epi.15.111
Source DB: PubMed Journal: Epigenomics ISSN: 1750-192X Impact factor: 4.778