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Targeting DNA Methyltranferases in Urological Tumors

Urological cancers are a heterogeneous group of malignancies accounting for a considerable proportion of cancer-related morbidity and mortality worldwide. Aberrant epigenetic traits, especially altered DNA methylation patterns constitute a hallmark of these tumors. Nonetheless, these alterations are...

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Autores principales: Marques-Magalhães, Ângela, Graça, Inês, Henrique, Rui, Jerónimo, Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909196/
https://www.ncbi.nlm.nih.gov/pubmed/29706891
http://dx.doi.org/10.3389/fphar.2018.00366
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author Marques-Magalhães, Ângela
Graça, Inês
Henrique, Rui
Jerónimo, Carmen
author_facet Marques-Magalhães, Ângela
Graça, Inês
Henrique, Rui
Jerónimo, Carmen
author_sort Marques-Magalhães, Ângela
collection PubMed
description Urological cancers are a heterogeneous group of malignancies accounting for a considerable proportion of cancer-related morbidity and mortality worldwide. Aberrant epigenetic traits, especially altered DNA methylation patterns constitute a hallmark of these tumors. Nonetheless, these alterations are reversible, and several efforts have been carried out to design and test several epigenetic compounds that might reprogram tumor cell phenotype back to a normal state. Indeed, several DNMT inhibitors are currently under evaluation for therapeutic efficacy in clinical trials. This review highlights the critical role of DNA methylation in urological cancers and summarizes the available data on pre-clinical assays and clinical trials with DNMT inhibitors in bladder, kidney, prostate, and testicular germ cell cancers.
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spelling pubmed-59091962018-04-27 Targeting DNA Methyltranferases in Urological Tumors Marques-Magalhães, Ângela Graça, Inês Henrique, Rui Jerónimo, Carmen Front Pharmacol Pharmacology Urological cancers are a heterogeneous group of malignancies accounting for a considerable proportion of cancer-related morbidity and mortality worldwide. Aberrant epigenetic traits, especially altered DNA methylation patterns constitute a hallmark of these tumors. Nonetheless, these alterations are reversible, and several efforts have been carried out to design and test several epigenetic compounds that might reprogram tumor cell phenotype back to a normal state. Indeed, several DNMT inhibitors are currently under evaluation for therapeutic efficacy in clinical trials. This review highlights the critical role of DNA methylation in urological cancers and summarizes the available data on pre-clinical assays and clinical trials with DNMT inhibitors in bladder, kidney, prostate, and testicular germ cell cancers. Frontiers Media S.A. 2018-04-13 /pmc/articles/PMC5909196/ /pubmed/29706891 http://dx.doi.org/10.3389/fphar.2018.00366 Text en Copyright © 2018 Marques-Magalhães, Graça, Henrique and Jerónimo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Marques-Magalhães, Ângela
Graça, Inês
Henrique, Rui
Jerónimo, Carmen
Targeting DNA Methyltranferases in Urological Tumors
title Targeting DNA Methyltranferases in Urological Tumors
title_full Targeting DNA Methyltranferases in Urological Tumors
title_fullStr Targeting DNA Methyltranferases in Urological Tumors
title_full_unstemmed Targeting DNA Methyltranferases in Urological Tumors
title_short Targeting DNA Methyltranferases in Urological Tumors
title_sort targeting dna methyltranferases in urological tumors
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909196/
https://www.ncbi.nlm.nih.gov/pubmed/29706891
http://dx.doi.org/10.3389/fphar.2018.00366
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