Epigenetics of Most Aggressive Solid Tumors: Pathways, Targets and Treatments

Highly aggressive tumors are characterized by a highly invasive phenotype, and they display chemoresistance. Furthermore, some of the tumors lack expression of biomarkers for target therapies. This is the case of small-cell lung cancer, triple-negative breast cancer, pancreatic ductal adenocarcinoma...

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Main Authors: Javier Martinez-Useros, Mario Martin-Galan, Maria Florez-Cespedes, Jesus Garcia-Foncillas
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/13/13/3209
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author Javier Martinez-Useros
Mario Martin-Galan
Maria Florez-Cespedes
Jesus Garcia-Foncillas
author_facet Javier Martinez-Useros
Mario Martin-Galan
Maria Florez-Cespedes
Jesus Garcia-Foncillas
author_sort Javier Martinez-Useros
collection DOAJ
description Highly aggressive tumors are characterized by a highly invasive phenotype, and they display chemoresistance. Furthermore, some of the tumors lack expression of biomarkers for target therapies. This is the case of small-cell lung cancer, triple-negative breast cancer, pancreatic ductal adenocarcinoma, glioblastoma, metastatic melanoma, and advanced ovarian cancer. Unfortunately, these patients show a low survival rate and most of the available drugs are ineffective. In this context, epigenetic modifications have emerged to provide the causes and potential treatments for such types of tumors. Methylation and hydroxymethylation of DNA, and histone modifications, are the most common targets of epigenetic therapy, to influence gene expression without altering the DNA sequence. These modifications could impact both oncogenes and tumor suppressor factors, which influence several molecular pathways such as epithelial-to-mesenchymal transition, WNT/β–catenin, PI3K–mTOR, MAPK, or mismatch repair machinery. However, epigenetic changes are inducible and reversible events that could be influenced by some environmental conditions, such as UV exposure, smoking habit, or diet. Changes in DNA methylation status and/or histone modification, such as acetylation, methylation or phosphorylation, among others, are the most important targets for epigenetic cancer therapy. Therefore, the present review aims to compile the basic information of epigenetic modifications, pathways and factors, and provide a rationale for the research and treatment of highly aggressive tumors with epigenetic drugs.
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spelling doaj.art-11d57e39a32f4c7fb0f48f9d762cb5b72023-12-03T13:09:56ZengMDPI AGCancers2072-66942021-06-011313320910.3390/cancers13133209Epigenetics of Most Aggressive Solid Tumors: Pathways, Targets and TreatmentsJavier Martinez-Useros0Mario Martin-Galan1Maria Florez-Cespedes2Jesus Garcia-Foncillas3Translational Oncology Division, OncoHealth Institute, Fundacion Jimenez Diaz University Hospital, Avenida Reyes Catolicos 2, 28040 Madrid, SpainTranslational Oncology Division, OncoHealth Institute, Fundacion Jimenez Diaz University Hospital, Avenida Reyes Catolicos 2, 28040 Madrid, SpainImperial College London, Exhibition Road, South Kensington, London SW7 2BX, UKTranslational Oncology Division, OncoHealth Institute, Fundacion Jimenez Diaz University Hospital, Avenida Reyes Catolicos 2, 28040 Madrid, SpainHighly aggressive tumors are characterized by a highly invasive phenotype, and they display chemoresistance. Furthermore, some of the tumors lack expression of biomarkers for target therapies. This is the case of small-cell lung cancer, triple-negative breast cancer, pancreatic ductal adenocarcinoma, glioblastoma, metastatic melanoma, and advanced ovarian cancer. Unfortunately, these patients show a low survival rate and most of the available drugs are ineffective. In this context, epigenetic modifications have emerged to provide the causes and potential treatments for such types of tumors. Methylation and hydroxymethylation of DNA, and histone modifications, are the most common targets of epigenetic therapy, to influence gene expression without altering the DNA sequence. These modifications could impact both oncogenes and tumor suppressor factors, which influence several molecular pathways such as epithelial-to-mesenchymal transition, WNT/β–catenin, PI3K–mTOR, MAPK, or mismatch repair machinery. However, epigenetic changes are inducible and reversible events that could be influenced by some environmental conditions, such as UV exposure, smoking habit, or diet. Changes in DNA methylation status and/or histone modification, such as acetylation, methylation or phosphorylation, among others, are the most important targets for epigenetic cancer therapy. Therefore, the present review aims to compile the basic information of epigenetic modifications, pathways and factors, and provide a rationale for the research and treatment of highly aggressive tumors with epigenetic drugs.https://www.mdpi.com/2072-6694/13/13/3209epigeneticmethylationacetylationnon-coding RNAsmall-cell lung cancertriple-negative breast cancer
spellingShingle Javier Martinez-Useros
Mario Martin-Galan
Maria Florez-Cespedes
Jesus Garcia-Foncillas
Epigenetics of Most Aggressive Solid Tumors: Pathways, Targets and Treatments
Cancers
epigenetic
methylation
acetylation
non-coding RNA
small-cell lung cancer
triple-negative breast cancer
title Epigenetics of Most Aggressive Solid Tumors: Pathways, Targets and Treatments
title_full Epigenetics of Most Aggressive Solid Tumors: Pathways, Targets and Treatments
title_fullStr Epigenetics of Most Aggressive Solid Tumors: Pathways, Targets and Treatments
title_full_unstemmed Epigenetics of Most Aggressive Solid Tumors: Pathways, Targets and Treatments
title_short Epigenetics of Most Aggressive Solid Tumors: Pathways, Targets and Treatments
title_sort epigenetics of most aggressive solid tumors pathways targets and treatments
topic epigenetic
methylation
acetylation
non-coding RNA
small-cell lung cancer
triple-negative breast cancer
url https://www.mdpi.com/2072-6694/13/13/3209
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